Journal Club with Dr. Peter Attia | Effects of Light & Dark on Mental Health & Treatments for Cancer

Welcome to the Huberman Lab Podcast where we discuss science and science based tools for everyday life. I'm Andrew Huberman and I'm a professor of Neurobiology and Ophthalmology at Stanford School of Medicine. Today marks the second episode in our Journal Club series with myself and Dr. Peter Attia. Dr. Peter Attia, as many of you know, is a medical doctor who is a world expert in all things healthspan and lifespan. He is the author of the best selling book Outlive as well as the host of his own terrific podcast the Drive. For today's episode, Peter and I each select a different paper to share with you. We selected these papers because we feel they are both extremely interesting and extremely actionable. First, I present a paper that is about how light exposure during the morning and daytime, as well as dark exposure at night, each have independent and positive effects on mental health as well as the ability to reduce the symptoms of many different mental health disorders. Now, I've talked before on this podcast and elsewhere about the key importance of seeing morning sunlight as well as trying to be in dim light at night. However, the data presented in the paper today really expands on that by identifying the key importance of not just morning sunlight, but getting bright light in one's eyes as much as is safely possible throughout the entire day, and a separate additive effect of being in as much darkness at night as possible. I describe the data in a lot of detail, although you do not need a background in biology in order to understand that discussion. And there's a key takeaway which is that if you can't get enough light in your eyes during the daytime, you would be well advised to get as much darkness exposure at night. In other words, light and dark have independent and additive effects on mental health. And during today's discussion, you'll learn exactly how to apply light exposure and dark exposure in order to get those benefits. Then Peter presents a paper about novel treatments for cancer. I must say, it's an extremely important conversation that everybody, regardless of whether or not you may have had cancer or know somebody who's had cancer, ought to listen to. He highlights the current technology of cancer treatments, as well as the future technology of cancer treatments, and the key role that the immune system and the autoimmune system play in treatments for cancer. I assure you that by the end of today's Journal Club episode, you will have learned a ton of new information about light and dark and mental health as well as cancer and the immune system and treatments for curing cancer. Before we begin, I'd like to emphasize that this podcast is separate from my teaching and research roles at Stanford. It is, however, part of my desire and effort to bring zero cost to consumer information about science and science related tools to the general public. In keeping with that theme, I'd like to thank the sponsors of today's podcast. Our first sponsor is eight Sleep eight Sleep makes smart mattress covers with cooling, heating and sleep tracking capacity I've spoken many times before on this podcast about the fact that sleep is the foundation of mental health, physical health and performance. Now, a key component of getting a great night's sleep is that in order to fall and stay deeply asleep, your body temperature actually has to drop by about 1 to 3 degrees. And in order to wake up feeling refreshed and energized, your body temperature actually has to increase by about to 3 degrees. One of the best ways to make sure that those temperature changes occur at the appropriate times at the beginning and throughout and at the end of your night when you wake up is to control the temperature of your sleeping environment. And that's what eight Sleep allows you to do. It allows you to program the temperature of your mattress and sleeping environment such that you fall and stay deeply asleep easily and wake up each morning feeling incredibly refreshed and energized. I've been sleeping on an eight sleep mattress cover for almost three years now and it has dramatically improved the quality of my sleep. So much so that when I travel and I' a hotel or an Airbnb and I don't have access to my eight sleep, I very much look forward to getting home because my sleep is always better when I sleep on my Eight Sleep mattress cover. If you'd like to try Eight Sleep, you can go to eightsleep.comhuberman to get $150 off their Pod 3 mattress cover. Eight Sleep currently ships in the USA, Canada, UK, select countries in the EU and Australia. Again, that's eightsleep.comhuberman Today's episode is also brought to us by BetterHelp. BetterHelp offers professional therapy with a licensed therapist carried out online. I've been going to therapy for well over 30 years. Initially, I didn't have a choice. It was a condition of being allowed to stay in school. But pretty soon I realized that therapy is extremely valuable. In fact, I consider doing regular therapy just as important as getting regular exercise, including cardiovascular exercise and resistance training, which of course I also do every week. The reason I know therapy is so valuable is that it if you can find a therapist with whom you can develop a really good rapport. You not only get terrific support for some of the challenges in your life, but you also can derive tremendous insights from that therapy, insights that can allow you to better not just your emotional life and your relationship life, but of course also the relationship to yourself and to your professional life, to all sorts of career goals. In fact, I see therapy as one of the key components for meshing together all aspects of one's life and being able to really direct one's focus and attention toward what really matters. If you'd like to try BetterHelp, go to betterhelp.comhuberman to get 10% off your first month. Again, that's betterhelp.comhuberman Today's episode is also brought to us by Joovv. Joovv makes medical grade red light therapy devices. Now, if there's one thing I've consistently emphasized on this podcast is the incredible role that light can have on our biology. And of course, I'm always telling people that they should get sunlight in their eyes as soon as possible after waking, on as many days of their life as possible and for sake of setting circadian rhythm, daytime mood, focus and alertness, and improve sleep. Now, in addition to sunlight, red light and near infrared light has been shown to have positive effects on improving numerous aspects of cellar and organ health, including faster muscle recovery, improved skin health and wound healing, even improvements in acne or that is, removal of acne, reducing pain and inflammation, improving mitochondrial function, and even improving vision itself. What sets Joovv apart and why it's my preferred red light therapy device is that it has clinically proven wavelengths, meaning it uses specific wavelengths of red light and near infrared light in combination that trigger the optimal cellar adaptations. Personally, I use the handheld Joovv every day. The handheld Joovv is about the size of a thick piece of toast, and I also own a Joovv panel that allows for full body exposure, and I use that one approximately five times per week for for about 10 to 15 minutes per session. If you'd like to try Joovv, you can go to Joovv spelled J-O-O-V-V.com Huberman Again, that's Joovv.com Huberman for this month only, January 2024, Joovv is offering exclusive discounts to Huberman Lab listeners with up to $500 off select Joovv products. Again, that's Joovv spelled J-O-O-V-V.com huberman to get up to $500 off select joovva products and now for my discussion with Dr. Peter Attia.

Andrew, great to have you here for Journal club number two. I'm already confident this is going to become a regular for us.

I'm excited. I really enjoy this because I get to pick papers I'm really excited about, I get to hear papers that you're excited about, and we get to sharpen our skills at reading and sharing data. And people listening can do that as well.

So last time I went first. So I think I'm going to put you in the hot seat first and have you go first, then I'll follow you.

Okay. Well, I'm really excited about this paper for a number of reasons. First of all, it, at least by my read, is a very powerful paper in the sense that it examined light exposure behavior as well as dark exposure behavior. And that's going to be an important point in more than 85,000 people as part of this cohort in the UK. I'll just mention a couple of things to give people background and I'll keep this relatively brief. First of all, there's a long standing interest in the relationship between light and mental health and physical health. And we can throw up some very well agreed upon bullet points. First of all, there is such a thing as seasonal affective disorder. It doesn't just impact people living at really northern locations, but basically there's a correlation between day length and mood and mental health, such that for many people, not all, but for many people, when days are longer in the spring and summer, they feel better, they report fewer depressive symptoms, and conversely, when days are shorter, significantly more people report feeling lower mood and affect. Okay, so there's a long standing treatment for seasonal affective disorder which is to give people exposure to very bright light, especially in the morning. The way that that's normally accomplished is with these SAD lamps, seasonal affective disorder lamps. And those lamps are basically bright, meaning more than 10,000 lux lights that they place on their kitchen counter or at their table in the morning or in their office. So they're getting a lot of bright light. That has proven to be fairly effective for the treatment of seasonal affective disorder. What's less understood is how light exposure in the middle of the night can negatively impact mood and health. And so where we are headed with this is that there seems to be, based on the conclusions of this new study, a powerful and independent role of both daytime light exposure and nighttime dark exposure for mental health. Now, a couple of other key points. The biological mechanisms for all this are really well established. There's a Set of cells in the neural retina, which aligns the back of your eye. They're sometimes called intrinsically photosensitive retinal ganglion cells. They're sometimes called melanopsin, retinal ganglion cells. We'll talk about those in a bit of detail in a moment. It's well known that those cells are the ones that respond to two different types of light input. Not one, but two different types of light input, and send information to the hypothalamus, where your master circadian clock resides. And then your master C and clock sends out secretory signals, so peptides, hormones, but also neural signals to the brain and body. And say, hey, now it's daytime, now it's nighttime. Be awake, be asleep. But it goes way beyond that. These melanopsin intrinsically photosensitive retinal ganglion cells, we know also project to areas of the brain like the habenula, which can trigger negative affect, negative mood. They can trigger the release of dopamine or the suppression of dopamine, the release of serotonin, the suppression of dopamine of serotonin. And so they're not just cells for setting your circadian clock. They also have a direct line, literally one synapse away into the structures of the brain that we know powerfully control mood. So, so the mechanistic basis for all this is there. So there's just a couple of other key points to understand for people to really be able to digest the data in this paper fully. There are basically two types of stimuli that these cells respond to. One is very bright light, as we just talked about. That's why getting a lot of daytime sunlight is correlated with elevated mood. That's why looking at a 10,000 lux artificial lamp can offset seasonal affective disorder, by the way.

Just a couple questions on that. How many lux does the sun provide on a sunny day at noon?

Okay, great question. So if you're out in the sun with no cloud cover or minimal cloud cover in the middle of the day at noon, chances are it's over 100,000 lux. On a really bright day, could be 300,000 lux. Okay. Most indoor environments, even though they might seem very bright, I like to think of your kind of like department store with the bright lights. Believe it or not, that's probably only closer to 6000 lux maximum, and probably more like 4000. Luxury most brightly lit indoor environments are not that bright when it comes down to total photon energy. Now, here's the interesting thing. On a cloudy day, when you're outside, it can be as bright as an average of a hundred thousand lux. But it won't seem that bright because you don't quote, unquote, see the sun. But it's also because when there's cloud cover, a lot of those long wavelengths of light, such as orange and red light aren't coming through. However, and this is so important, the circadian clock, the suprachiasmatic nucleus, it sums photons, it's a photon summing system. So basically, if you're outside in 8000 lux, very overcast UK winter day, and you're walking around hopefully without sunglasses, because sunglasses are going to filter a lot of those photons out, your circadian clock is summing the photons. So it's an integration mechanism. It's not triggered in a moment. And actually the experiments of recording from these cells, first done by David Burson at Brown, were, you know, historic in the field of visual neuroscience. When shown bright light on these intrinsically photosensitive cells, you could crank up the intensity of the light and the neurons would ramp up their membrane potential and then start spiking, firing action potential, long trains of action potentials that have been shown to go on for hours. And so that's this signal that's propagating into the whole brain and body. Okay, so the, the important thing to understand is this is not a quick switch. That's why I suggest on non cloudy days, we'll call them that people get 10 minutes or so of sunlight in their eyes in the early part of the day, another 10 minimum in the later part of the day, as much sunlight in their eyes as they safely can throughout the day. But since you're a physician, I should just. And you had a guest on talking about this recently. When the sun is low in the sky, low solar angle sunlight, that's really the key time for reasons we'll talk about in a moment. And when the sun is low in the sky, you run very, very little risk of inducing cataract by looking in the general direction of the sun. You should still blink as needed to protect the eyes. It's when the sun is overhead and there's all those photons coming in quickly in one, in a short period of time that you do have to be concerned about cataract and macular degeneration if you're getting too much daytime sunlight. So the idea is sunglasses in the middle of the day are fine, but you really should avoid using them in the early and later part of the day unless you're driving into the sun and you need you know, for safety reasons.

Another question, Andrew. Yeah. If, if a person is indoors, but they have large windows, so there's, they're getting tons of sunlight into their space, they don't even need ambient indoor light. How much of the photons are making it through the glass and how does that compare to this effect?

Yeah, in general, unless the light is coming directly through the window, most of the relevant wavelengths are filtered out.

In other words, if you can't see the sun through the window, even if sufficient light is being provided, that's insufficient to trigger this phenomenon.

That's right. However, if you have, you know, windows on your roof, which some people do, skylights, that makes the situation much, much better. In fact, the neurons that in the eye that signal to the circadian clock and these mood centers in the brain reside mainly in the bottom two thirds of the neural retina and are responsible for looking up, basically they're gathering light from above. These cells are also very low resolution. So think of them as big pixels. They're not interested in patterns and edges and movement. They're interested in how much ambient light there happens to be. Now, keep in mind that this mechanism is perhaps the most well conserved mechanism in cellular organisms. So there. And I'll use that as a way to frame up the four types of light that one needs to see every 24 hours for optimal health. And, and when I say optimal health, I really mean mental health and physical health. But we're going to talk about mental health mainly today in this paper. There's an absolutely beautiful evolutionary story whereby single cell organisms, all the way to humans, dogs, rabbits and everything in between, have at least two cone opsins, one that responds to short wavelength light, AKA blue light, and another one that responds to longer wavelength light, orange and red. So your dogs have this, we have this, and it's a comparison mechanism in these cells of the eye, these neurons of the eye, they compare contrast between blues and orange, or sometimes blues and reds and pinks, which are also all long wavelength light. There are two times of day when the sky is enriched with blues, oranges, pinks and reds, and that's low solar angle sunlight at sunrise and in the evening. These cells are uniquely available to trigger the existence of those wavelengths of light early in the day and in the evening, not in the middle of the day. So these cells have these two cone photopigments and they say how much blue light is there, how much red light or orange light? And the subtraction between those two triggers the signal for them to fire the signal off to the circadian clock of the brain. And that's why I say look at low solar angle sunlight early in the day. What that does is it what call it as phase advances the clock. This can get a little technical, and we don't want to get too technical here, but think about pushing your kid on a swing. The period of that swing, the duration of that swing is a little bit longer than 12 hours. Okay? So when you stand closer to the kid, so your kid swings back and you give it a push, you're shortening the period, right? You're not allowing the swing to come all the way up. That's what happens when you look at morning sunlight. You're advancing your circadian clock. Translate to English or non nerd speak. You're making it such that you will want to go to bed a little bit earlier and wake up a little bit earlier the next day. In the evening, when you view low solar angle sunlight. So in the after the afternoon setting sun or evening setting sun, you do the exact opposite. You're phased, delaying the clock. It's the equivalent of your kid being at the very top of the arc. And so it's gone, you know, maybe 12 and a half hour, 12, let's say 12 and a half hours is the duration of that swing. And you run up and you push them from behind and give them a little more push. That's the equivalent of making yourself stay up a little later and wake up a little later. These two signals average so that your clock stays stable, you don't drift, meaning you're not waking up earlier every single day or going to sleep later every single day. This is why it's important to view low solar angle sunlight in the morning and again in the evening as often as possible. And it's done by that readout of those two photopigments. Now, midday sun, which contains its bright light, but you see it as white light, contains all of those wavelengths at equal intensity. So the middle of the day is the so called circadian dead zone. In the middle of the day, bright light triggers the activation of the of the other opsin, the melanopsin, which increases mood, increases feelings of well being, has some other consequences. But you can't shift your circadian clock by viewing the sun in the middle of the day because it's in the circadian dead zone. It's the equivalent of pushing your kid on the swing. When they're at the bottom of the arc, you can get little bit more, but not much. And in biological terms, you get nothing. So this is why looking at sunlight in the middle of the day is great, but it's not going to help anchor your sleep wake cycle. And if you think about this is incredible, right? Every organism from single cells to us has this mechanism to know when the sun is rising and when the sun is setting. And it's a color comparison mechanism which tells us that actually color vision evolved first not for pattern vision, not for seeing beautiful sunsets and recognizing that's beautiful or paintings or things of that sort, but rather for setting the circadian clock.

Now, what if you only do one of these? Andrew, so what if you've got constant exposure to low morning light, but your job prevents you from doing the same in the evening or vice versa?

Yeah, a great question. Better to get the morning light because if you have to pick between low solar angle light earlier, later in the day, and keep in mind if you miss a day, no big deal. It's a slow integrative mechanism averaging across the previous two or three days. But if you miss a day, you'll want to get twice as much light in your eyes that next morning. The reason it's better to do in the morning as opposed to the evening, although both would be to do best would be to do both, excuse me, is that most people are getting some artificial light exposure in the evening anyway. And here's the diabolical thing. Your retina is very insensitive to light early in the day. You need a lot of photons to trigger this mechanism early in the day. As the day goes on, retinal sensitivity increases and it takes very little light to shift your circadian clock late in the day. Keep in mind also that if you do see afternoon and evening sunlight, there's a beautiful study published in Science Reports, yes, Science Reports two years ago showing that that can partially offset the negative effects of artificial light exposure at night. I think of this as your Netflix inoc. The amount of melatonin suppression from nighttime light exposure is halved by viewing evening setting sun. Now keep in mind, you don't need to see the sun cross the horizon. It can just be when it's low solar angle. So you're looking for those yellow, blue or blue, pink, blue, red, contrast. And on cloudy days, believe it or not, they're still there. Just you don't perceive as much of it coming through. So they're really. So that's three things that we should all strive to do. View low solar angle sunlight early in the day, view solar angle sunlight later in the day, and get as much bright light in our eyes as we safely can, ideally from sunlight throughout the day. And if you can't do that, perhaps invest in one of these satellites, although they can be a bit expensive. There are a couple companies that are starting to design sunrise simulators and evening simulators that are actually good, that actually work. But right now my read is that aside from one company out there which by the way I have no relationship to, it's called the Tuolight T u O. And that light bulb was developed by the biologists at the University of Washington who basically discovered these color opponent mechanisms. Those lights are not particularly expensive, but they're, they do seem to work. In fact they're the study that is emerging. Again, unpublished data seems to indicate that if you look at it for more than five or six minutes, it can induce a mild euphoria. That's how powerful this contrast is. And what they did there in that light, I'll just tell you the mechanism is they figured out that when most people look at low solar angle sunlight in the morning, they're getting 19 reversals of blue, orange per second. So when you look at this light, it looks like a barely flashing white light, but it's reversals of orange and blue, orange and you know, red and blue and it's happening.

And so what does the person looking at it perceive?

Well, I've used one of these. It just looks like a flickering light and of course there's always the potential of a placebo effect, but that's what.

I was going to say. Is there a way to control for that by having something that looks the same to the user but of course is not producing the same photo effect?

Yeah, well they've done that with the 10,000 lux SAD lamps and you would and which most people use to try and induce sunrise simulation in their home. But keep in mind that sunrise gives you this comparison of short and long wavelength light. Just a bright 10,000 lux light triggers one of the opsins that that but it won't set your circadian clock. So most of the SAD lamps that are out there are activating only one of the mechanisms in these cells that's relevant and not the one that's most relevant. So I'm excited about what 2o is doing. I think that. And again I have no relation to them except I know the biologists who did the work that provide the mechanistic logic for that engineering. I still think we're in the like, the really like early days of this stuff. What should be done is to have this stuff built into your laptop.

Right.

It should be built into your phone and hopefully it will be. Now, I mentioned this color contrast thing in sunrise and sunset. I mentioned the bright light throughout the day. But there's a fourth light stimulus that turns out to be really important, and this will provide the segue into the paper. Turns out that dark exposure at night, independent of light exposure during the day, is important for mental health outcomes. Now, most people think dark exposure. How do I think about that? Well, it is dark, yet it's the absence of light. But what this paper really drives home is that people who make it a point to get dark exposure at night, AKA the absence of light at night, actually benefit even if they're not getting enough sunlight during the day. And this is especially true for people with certain mental health issues. So I don't think we can overstate the value of. Of accurately timed light exposure to the eyes in the context of mental health. I think, you know, there's so much data by now. I will say, however, that some people seem more resilient to these light effects than others. Meaning some people, you know, also don't suffer from jet lag too much. Some people can stay up late, get a lot of bright light exposure in the middle of the night, and during the day, they've got their sunglasses on all day and they're in a great mood all the time. Other people are more susceptible these sorts of things. And we don't know whether or not polymorphisms underlie that. I personally am very sensitive to sunlight in the sense that if I don't get enough sunlight, I don't feel well after a couple of days. But I'm less sensitive to light exposure at night, for instance. But I think it is, perhaps this is a big statement, but is perhaps the most fundamental environmental stimulus for levels of arousal and alertness, which correlate with all sorts of, you know, neuromodulator and hormone outputs. And so none of this should come as any surprise. I will mention one last thing. There was a study published, gosh, over 10 years ago now from Chuck Zeisser's lab at Harvard Medical School, phenomenal lab exploring circadian human health behavior. He's just considered a, no pun, a luminary in the field. But there wasn't a study that was in error where they had published in Science magazine that light shown behind the knee could shift circadian rhythms. And that paper was retracted, and a lot of people don't know that it was retracted. Light exposure to the eyes is what's relevant here. And as far as we Know the color of one's eyes, like darkness or lightness of one's eyes bears no relevance on their sensitivity to these types of mechanisms. And on and on.

So one question, one comment. The question again is going back to the morning evening light. And I spend a lot of time, more time looking at those types of skies, for example, just because of the nature of my hobbies, right? Because I'm always doing archery in the morning and rucking in the afternoon. So it's not uncommon that I'm seeing both of those. How relevant is it that the sun be above the horizon? So, for example, it begins to get light about in 30 minutes before sunrise and then, you know, right. So if sunrise is at 7:30, first light is 7 and then, you know, sort of 7:15 to 7:30 is actually quite bright. I mean, you can see anything and everything. And the same is true at sunset. So does, does that 30 minutes pre or when sun is beneath the horizon constitute part of that 10 minutes?

It does. I mean, in an ideal circumstance you'd get outside and see the sunrise every day and you'd see the sunset every day, even on cloudy days. Some people like myself wake up before the sun comes up, in which. And I get this question all the time. Well, in the absence of powers to make the sun rise faster, which I'm not aware anyone has, certainly not me, I think the best thing to do is simply to turn on as many bright lights as you can indoors to trigger that melanopsin mechanism. If you want to be awake, if you want to stay asleep or sleepy, then keep them dim and then get outside once the sun is starting to come out. Some people wake up after the sun has risen, right? In which case get what you can. And some people wake up 10am or noon, in which case you can still get the bright light exposure, but you won't shift your circadian clock. Now, in the evening, especially in the winter months, it's important to look west and try and get some sunlight in your eyes in the evening. If you've ever gone into the clinic, for instance, at 2 o' clock in the afternoon after lunch, you know, and then in the winter, and then come out and it's dark when you're walking to your car, it's a kind of eerie feeling. That sort of eerie feeling may correlate with the fact that you missed a signal. Your brain is trying to orient your brain and body in time. And that's what all of this is, right? It's trying to orient in time. And again, some people are more susceptible to that than others. Some people might like that feeling of, oh, I went in when it was bright and I come out when it's dark. But the vast majority of people feel better when they're getting this morning and evening sunlight exposure. And this is especially important in kids. All right, this is one of the things that, you know, this paper points out, and there are good data that people are spending approximately 90% of their time indoors nowadays. Daytime time indoors, and those indoor environments are simply not bright enough. You think, oh, there's all these bright lights and some people are putting blue blockers on in the middle of the day, which is the worst thing you could possibly do if you're going to wear blue blockers. And I don't think they're necessary, but if you're going to wear them, you'd want to wear them at night. And in the evening, you don't need to wear blue blockers. You just simply should dim the lights and ideally have lights that are set a little bit lower in your environment, which the Scandinavians have been doing for a long time. So, you know, kill the overhead lights and don't obsess about bright light exposure in the middle of the night. In fact, for a long time, I and some other people were saying, oh, you know, even just a brief flash of light in the middle of the night can quash your melatonin. That's true. But the other time in which you're in this quote unquote circadian dead zone is in the middle of the night. You can't shift your circadian clock in the middle of the night. But, you know, all of this gets down to interweaving rhythms of light sensitivity, temperature, hormone output, cortisol, it. I mean, there's a whole landscape of circadian biology. This paper, which was published in a new journal that I'm really excited about called Nature Mental Health, this journal was just launched recently, is entitled Day and Night Light Exposure are Associated with Psychiatric Disorders and Objective Light Study in more than 85,000 people. Now, I have to say that I think the title of this paper is Terrible. Sorry, folks at Nature Mental Health, because if one just read the title, it sounds like Day and Night Light Exposure Associated with Psychiatric Disorders. Right, right. If this were, if this were a newspaper headline, you'd be like, oh, my goodness, well, what are you supposed to do? Right? But that's not the conclusion. The conclusion is that getting a lot of sunlight exposure during the day and getting a lot of dark exposure at night is immensely beneficial for psychiatric Health and in a number of ways. Now, I'm not one to bring up another paper unannounced, but I will say that this paper built off a previous study entitled time spent in outdoor light is associated with mood, sleep and circadian rhythm related outcomes. And that was a cross sectional longitudinal study in 400,000 Biobank participants. So this UK Biobank is an incredibly valuable resource and there are now multiple studies establishing that one's pattern of light exposure is extremely important. Now, the previous study in 400,000 participants basically nailed home the idea that the more time you spend outdoors, the better is your mood, the better is your sleep, the better is the rhythmicity of your sleep wake cycles and on and on. Something that I think even though people will say we've known that for thousands of years needed scientific substantiation, this new study essentially looked at the relative contributions of daytime light exposure and nighttime dark exposure. And they did that on a background of looking. In particular people who had major depressive disorder, generalized anxiety, ptsd, bipolar disorder. Here's the basic takeaway and I'll quote them here and then I'll tell you my interpretation that here I'm quoting avoiding night at light and seeking light during the day. I love that word. Seeking may be a simple and effective non pharmacologic means for broadly improving mental health. So that's a pretty bold statement, right? And I love that they say seeking because it implies that people aren't reflexively getting the light exposure that they need, that this needs to be a practice much like zone 2 cardio or resistance training. Okay, so what did they do in this study? So basically they gathered up a hundred thousand people or so. It eventually was pared down to about 86,000 participants because some just didn't qualify or didn't report their data back. They equipped them with accelerometers on their wrists. And those wrist devices also could measure ambient light. Now that's not a perfect tool because what you'd love to do is measure ambient light at the level of the eyes. By the way, will somebody design an eyeglass frame that changes color when you've gotten sufficient light from sunlight during the day, and then, and then at night is a different color. And then if you're getting too much light exposure, we'll go to a different color frame. This has to be possible so that you don't have to wonder if you got enough light during the day. And of course, if it's at the level of the eyes, then you know, that's what's landing at the eyes.

Yeah. And it's less. I mean that's what I was going to ask you about that. Do these wrist based devices potentially get covered by clothing and some turned over. You have your sleeves down? I have my sleeves up.

They had it on the outside of the sleeve, but they asked that people just keep it on their dominant hand. It's not perfect, but in some ways it's kind of nice that it's not perfect. We could turn that disadvantage into advantage by thinking, you know, when the person is out and about, they're not often looking right at the sun. You know, if you're talking to a colleague under an overhang, for instance. So it's, it's not perfect, it's directionally. Right, okay. And then they had two hypothesis hypotheses, two primary hypotheses. One, that greater light exposure in the day is associated with lower risk for psychiatric disorders. And two second hypotheses, greater light exposure at night is associated with higher risk for psychiatric disorders and poorer mood. This is oh so relevant for the way we live now. People on screens and tablets in the middle of the night. Okay. Then they collected information about how much light exposure people were getting as well as their sleep and their activity and so on. I should mention this was done in males and females. It was a slightly older cohort than one is used to seeing people in their 50s and 60s. They had psychiatric diagnosis information and then they divided people into essentially two groups, but they had a lower, so a Q1 and a Q2, a lower quartile. That meant people that were getting less daytime light as opposed to the third and fourth quartile, more daytime light. They also had a nighttime light exposure evaluation and they had people in the low Q1 and Q2. So these people are getting less nighttime light versus Q3, Q4, more nighttime light. Nicely. They also looked at sleep duration and they looked at photo period, meaning how long the days were for those individuals, how active they were. Look, 10 hours a day, 14 hours a day. Because the more active you are, the more opportunity for light exposure you have during the day or night, for instance. Okay. So it. They had, I would say fairly complete data sets then. And I'm just going to kind of hit the top contour of what they.

Did in each and sorry, sleep duration, sleep efficiency, etc was determined off the accelerometer.

That's right. As well as self report. Yeah. Not. Not ideal. Right. You'd love to. For people to be wearing a whoop band or, or a ring or something of that sort of but this was initiated some time ago. So they either didn't have access to that technology or for whatever reason, didn't select it. I'd like to take a brief moment and thank one of our sponsors, and that's AG1. AG1 is a vitamin mineral, probiotic drink that also contains adaptogens. I started taking AG1 way back in 2012. The reason I started taking it and the reason I still take it every day is that it ensures that I meet all of my quotas for vitamins and minerals, and it ensures that I get enough prebiotic and probiotic to support gut health. Now, gut health is something that over the last 10 years, we realized is not just important for the health of our gut, but also for our immune system and for the production of neurotransmitters and neuromodulators, things like dopamine and serotonin. In other words, gut health is critical for proper brain functioning. Now, of course, I strive to consume healthy whole foods for the majority of my nutritional intake every single day. But there are a number of things in AG1, including specific micronutrients that are hard to get from whole foods or at least in sufficient quantities. So AG1 allows me to get the vitamins and minerals that I need. Probiotics, prebiotics, the adaptogens, and critical micronutrients. So anytime somebody asks me if they were to take just one supplement, what that supplement should be, I tell them AG1, because AG1 supports so many different systems within the body that are involved in mental health, physical health, and performance. To try AG1, go to drinkag1.comhuberman and you'll get a year supply of vitamin D3K2 and five free travel packs of AG1. Again, that's drinkag1.comhuberman then what they did is they got. They have information on who has major depressive disorder, who has PTSD, generalized anxiety, bipolar psychosis, etc. And then they ran three models. And you can tell me what you think about the power of these models. But, you know, as somebody who thinks about the mechanistic aspect of all of this a lot, but not somebody who's ever run this type of study, I'd be really curious. Model 1 examined the unadjusted association between day and nighttime light exposure and psychiatric outcomes. So just basically asking, is there a relationship between how much light you get during the day and how much light you get at night and how bad your or your depression is or anxiety is, et cetera? Looking at, you know, just a standard ratio of the probability that you have a certain symptom or set of symptoms versus you don't, given a certain amount of light exposure. Model 2 adjusted for the age of the person, their sex and ethnicity and photo period. So they looked at, you know, how long the days were in that given person's region of the world. And then model three, these people were.

All in the UK or were they around?

They were all in the uk, as far as I know. And then model three adjusted for employment. So employed versus unemployed, which if you think about it, is pretty important. Like you say, well, an unemployed person has a lot more time to control these variables, but an employed person who's doing shift work does not. Right. And they, they incorporated information about employed versus unemployed physical activity, which turns out to be very important, and then things like shift work, etc. And so these, what we can say very safely is that the outcomes with each of these models, the results were very similar. So we don't want to discard the differences between those models entirely. But in my read is in every figure of the paper, it doesn't seem like model one, two or three differ from one another in terms of total outcome.

Yeah, that's an unusual aspect of this paper. So these adjustments are very standard, right? So this is a classic tool that's used in most epidemiology because you don't have randomization. So once randomization is out the window, you know, you're like, so for example, the paper I'm going to present is based on an rct. There will be no models, it's just here are the data, right?

Yeah. Here they're asking people, what, what do you do? Report back to us. We're going to measure your light exposure. But no one was assigned any groups or swapped whatever quote, unquote controls are there, they're really not there. It's just comparisons between groups.

So what is interesting to me is that it's exactly as you said and we'll make all these figures available in addition to the papers. But I mean there, it's very unusual that there's no difference between the unadjusted and the adjusted models. And as you say, there's probably two places out of, you know, 30, when you look at all the different quartile comparisons where you might creep from, you know, statistically significant just out of it or just into it. But yeah, you could simplify this figure 2 completely by just showing one of the models and you would be, you know, getting 95% of the information, which is, you know, I mean, I think in one way that suggests that there's less dependency on those variables. Of course, it still doesn't address probably the greatest question I have here, which I'm sure we'll get to at some point as you continue.

Yeah. So I'm very curious what that question is, but I'll suppress my curiosity for the moment. So if we look at Figure 2 of this paper, and I realize a lot of people are listening and they're not able to look at this, although we have posted the figures on the YouTube versions of this. Just want to make clear what's going on. Just for those that are listening, essentially what they're looking at is what they call the odds ratio, which is the probability of something happening in one group versus divided by the probability of something happening another group, I guess would be it by way of example, would be, you know, if you're going to look at the odds ratio of, you know, the probability of somebody getting lung cancer if they smoke versus probability somebody getting lung cancer if they don't smoke.

So odds ratios and hazard ratios are often confused. They're very similar. And odds ratios generally refer to a lifetime exposure, whereas a hazard ratio is defined over a specific period of time. But the math is still effectively the same. And using the example you gave, if you took the odds ratio of, you know, death. So let's talk all cause mortality for a smoker versus a non smoker, and the answer were 1.78. I'm making that up, but that's directionally correct. 1.78 as an odds ratio means there's a 78% chance greater of the outcome of interest, in this case, death by any cause in the affected group, which would be the smokers. So odds ratio of two is 100%. An odds ratio of three is 200%. So the math is take the number, subtract one and that's the percent.

You know, figure two of this paper is one of the key. Take homes. They essentially look at the odds ratio of people who are in the. Let's say that let's just look at.

The nighttime light exposure and just remind me, Andrew, because. And everybody else watching every one of these is showing 2nd, 3rd, 4th as your X axis.

Right.

Meaning they're all being compared to the first quartile.

That's right.

And the first quartile is lowest light exposure or highest light exposure lowest.

Well, or. Well, we have to differentiate between day and night. That's right.

Okay, so restate it. Sure.

So if we look at, you know, what is your risk of a psychiatric challenge, broadly speaking. Well, panel A is major depressive disorder if you are in the second quartile, third quartile, or fourth quartile of night time light exposure. So second being the least amount of nighttime light exposure, third being more nighttime light exposure, and fourth, the most nighttime light exposure relative to the first quartile.

This is just a stupid thing. Like if I were doing this figure, if you were doing this in a lecture, you know what you would do to make it so easy? You would draw arrows on it that say, increasing light exposure at night, decreasing light exposure in the day. It's the same information. It just makes it easier for the reader to understand.

Absolutely.

But maybe the teaching point, I think is for people when they review articles like don't be afraid to do that and just kind of like, oh, I. Exactly. So it's like I draw the arrow that's increasing light, that's decreasing light, and that's how I can pay attention to what's actually happening. Right.

And I'm actually in touch with the editorial staff at Nature, at Nature Mental Health, although they don't know that I'm covering this paper until after this comes out. You know, I think one thing that scientific journals really, really need to do is start making the readability of the articles better for non experts. I mean, chances are if you can't understand a graph, and this is true for everybody, chances are there's a problem with the way it's presented. Yeah, put it on them. But then of course try and parse it because, you know, rarely, if ever is it all spelled out clearly. But anyway, that's what we're trying to do here. So yeah, the way I would have done is say second quartiles, low amounts of nighttime light exposure and define what that is. You know, third quartile is more light exposure and then fourth, maximum amount of light exposure at night. And basically what you see is that the probability of having worse major depressive symptoms linearly increases as you go from the second to third to fourth quartile. So more nighttime light exposure, worse for you. And there's a dose response, if you will, of the effect. Now we can march through or describe Figure 2 pretty quickly by saying the same thing is true. Now we're just talking about nighttime light exposure for generalized anxiety disorder. So that's panel C, bipolar disorder. Although the difference between the second and third quartile and bipolar disorder isn't as dramatic Once you get up to the fourth quartile, Bipolar symptoms get much worse when people are Getting nighttime light exposure. I really want to emphasize that point because they go on in the discussion of this paper to re emphasize that point several times. In fact, they say that while light exposure during the day, of course we will go into the data. Is beneficial for mental health. For people with bipolar disorder, it seems that light exposure at night is especially problematic independent of how much sunlight they're getting during the day. So you're bipolar. In the person with bipolar disorder who's struggling with either a manic or depressive episode, who's making a point to get sunlight during the day, who's also getting light exposure at night, is making their symptoms worse. And keep in mind, they, they couldn't completely control this, but this is largely independent of things like sleep duration. So that doesn't necessarily mean that the person's sleeping less, although in a, in a manic episode, presumably they are. It's independent of exercise. It's independent of a bunch of other things because any, any logical person will hear this and say, okay, well, they're getting more light at night because they're doing a bunch of other things, but it's largely independent of those other things. Likewise, the symptomology of PTSD gets far worse with increasing light exposure at night. Self harm really takes a leap from being fairly, I don't want to say minimal at the second and third quartile. So low and let's say medium, I'm using some, I'm taking some liberties here, but low and medium amounts of, of artificial light exposure at night. Then for people who get quite a lot of nighttime light exposure, self harm goes up and probability of psychotic episodes goes up or psychotic symptoms. Now, what's nice is that what's nice about the data is that the exact inverse is basically true for daytime light exposure, although not across the board. We can generally say that for major depressive disorder, generalized anxiety, bipolar symptoms, there it's a little more scattered PTSD and self harm, the more daytime light exposure, ideally from sunlight, because that's actually what's being measured in most cases. We could talk about how we know that is going to approximately linearly drop the probability or the severity of these symptoms.

And we could just explain again that the odds ratios now seem to be going down. So an odds ratio of 0.7 now refers to a 30% reduction in the variable of interest here.

Exactly. Now, the psychosis panel F, which focuses on psychosis, I think is also worth mentioning in a bit more detail. There's a fairly dramatic reduction in psychotic symptoms as one gets more daytime Light exposure independent of nighttime light exposure. There's a well known phenomenon called ICU psychosis, which is that people come into the hospital for a broken leg or a car accident. Maybe they were getting surgery from, from Peter back when for something totally independent. They're, they're housed in the hospital. And as anyone who's ever been in a hospital as a patient or visitor knows, the light in the lighting environment, the hospital is absolutely dreadful for health, just dreadful. I mean, people often complain about the food in the cafeteria as being unhealthy. That's often. Not always true. Not always true. But the lighting environments in hospitals is.

Absolutely counterpart, especially in the intensive care unit. Yeah, right. So I think the intensive care unit at Hopkins, the main one, the main sicu, didn't have windows.

People who go into the hospital with a brain injury or with a stroke or something, I get contacted all the time, even though I'm not a clinician. What should I do for my kid, my parent? I always say get them near a window and start to the best of your abilities, controlling their sleep, wake cycle. Now oftentimes there's their, you know, nurses coming in and taking blood tests and measuring pulses in the middle of the night. That's disruptive. There, there's bright light, not just blue light. That's disruptive. It's noisy. That's disruptive. ICU psychosis is when non psychotic individuals start having psychotic episodes in the hospital because of nighttime light exposure and in some cases lack of daytime sunlight. We can say that with some degree of confidence because when those people go home, even though sometimes their symptoms for what brought them to the hospital in the first place get worse, their psychosis goes away now and it's independent of medication. So let's just be really direct. There is a possibility that we are all socially jet lagged, that we are all disrupting these mood regulation symptoms systems. Excuse me, by not getting enough daytime light and by getting too much nighttime light. If we want to look at just some of the bullet points of the takeaways and Peter, thank you. You highlighted a few of these, but.

Can we just go back to this figure 2 for a second?

Oh, yeah, sure.

There's a handful of things that I.

Knew Peter was going to want to, want to dig in the data.

Yeah, yeah. And again, I normally wouldn't make so much hay out of this except for the fact that they're so tight, but the there are a few that really stand out. And again, I love this figure. I would have labeled it a little differently to make it completely user friendly. But nevertheless the increasing light at night and the impact on depression. Let me be really technical in what I say. And the relationship or correlation to depression is very strong. The relationship to light and self harm in the upper quartile. So when you take those 25% of people with the most nighttime light, that relationship to self harm is interesting. And completely uncoupled from the other 75%. That's interesting.

By uncoupled you mean that at the lower levels of light exposure at night you're not seeing an increase in self harm.

Not what's.

And then once you get to that.

Fourth quartile, it's a big step.

It's a like a 30% greater risk of self harm.

Yeah. So it's totally flat. The first, second, third quartile. No different. And then fourth big jump. And then the, the, the inverse relationship. Right. As light increases during the daytime, you see this reduction in self harm. Interesting. The PTSD relationship based on nighttime light and the psychosis relationship based on daytime light, those are the ones that really jumped out to me. I think anxiety relatively the you know, less impressive here and bipolar disorder didn't seem as strong.

Right.

As well. So I think those, those are the big ones that I agree. That jumped out to me.

Yeah, I agree there's a, there's a bit more scatter on generalized anxiety and the degree of the signif. The degree of significant change is not, is not as robust. In other words, getting a lot of daytime light, ideally from sunlight is not necessarily going to reduce your levels of anxiety. Getting a lot of nighttime light exposure is not going to not increasing nighttime anxiety that much. Although 20%, you know, is, is not nothing for nighttime light exposure. But yeah, where the psychosis, major, major depression and self harm are really, you know, they leap out. Actually we maybe we even just drill a little bit deeper on major depression. And basically when you go from the second to third quartile of nighttime light exposure, so more nighttime light exposure, you basically go from no significant increase to almost, almost a 20% increase. And then as you get up to the fourth quartile, so the most nighttime light exposure, you're at about 25% increase in major depressive symptoms. That's no joke. And you know, and I think that, I think that we, you know, if we were to, I mean we don't have the data right here, but if we were to look at like a standard SSRI treatment for major depression. You know, people debate this pretty actively, but light is a very potent stimulus and the Timing of light is critical because on the, the inverse is also true. As you get to the fourth quartile of daytime light exposure, you get about a 20% reduction in major depressive disorder.

What I like about a study like this is that it puts the error bars so easy to see on the data. And why is that interesting? Well, there's, there's, there's a, there's a belief that bigger is always better in sample size. And we often talk about that through the lens of power analysis. Right. So how many subjects do we need to, to, to reach a conclusion that is powered to, you know, this level? And that's, that's true. But what I don't think gets discussed as often is the opposite of that, which is what if you overpower a study? In other words, what if the power anal analysis says to be, to have a level of power at 90%, you need a thousand subjects and you say, great, we're going to do 10,000 subjects. Well, you're clearly powered for it, but you might be overpowered and people might say, well, why would that be a bad thing? It could be a bad thing because it means you are very likely to reach statistical significance in things that might not be actually significant. And so one thing about this study that is just a quick back, like kind of a quick and dirty way to tell that it's probably not overpowered is that you have varying lengths of error bars. And what that tells me is that, and again, this is not like a formal statistical analysis, it's just kind of like a back of the envelope statistical analysis. If you look for example, at self harm in the top quartile, you actually have pretty big error bars. In fact, all the self self harm have sort of slightly bigger error bars. And yet when you look at for example, the depression, even though the error bars aren't all the same size, they're tighter. In fact, when you look at the relationship between depression and daytime light, the error bars are really, really small. So that just gives me confidence that there is variability in this, which paradoxically you kind of want to see because it tells me that this wasn't just done, you know, there was, I think you said 8,000 subjects were in this.

And I realized 80 more than 86,000.

86,000. Sorry.

Yeah.

You realize that it wasn't that, oh, this should have been done with a tenth of that or a half of that. And we're picking up signal that is statistically relevant but clinically irrelevant.

Yeah, thanks for, for that point that I didn't pay attention to that. I mean, I paid attention to the error bars, but I didn't know that. So thank you. I'm learning too. And I suppose for people that are listening, we can just give them a sense of what the error bar ranges are for self harm. You know, they're running, you know, as much as 20% either side of the mean, the average. And for major depression it looks like it's more like, let's say 8 to 10%, if, if that 5. Right, so, yeah, I see what you're saying. So when you get a, a very large sample size, you're going to have some outliers in there and you can mask those outliers just by having so many data points, right?

Yeah, because these error bars directly tell you whether or not you're statistically significant. So what's really nice about this type of graph, and you see these in. There's going to be a graph in my paper where you see the same analysis, they're always drawing the 95% confidence interval on the, on the data point. And if the 95% confidence interval does not touch the, the line of unity, which in this case is the HODS ratio of 1.0 or the X axis, then you know, it's statistically significant to the confidence interval they've defined, which is almost assuredly 95%. Sometimes they'll make it tighter at 99. And so that's why you can just look right at these and go, oh, look. You know, in depression, the second quartile didn't reach statistical significance because the error bars are touching the line, just as the case for the second and third quartile for self harm. But when you look at the fourth quartile, you can see that the lower tip of the error bars isn't anywhere near unity. And so we know without having to look up the p value that it's smaller than either 0.05 or 0.1, however they've defined it. And it's really amazing when you see these, you know, overpowered studies which are easier to do epidemiologically, where, you know, the P value ends up being microscopic. You know, they can, they can drive their P values down to anything low because sample size can be infinite. But you know, you can see that it's just like the, the error bar is just skimming above the, the, the unity line, but it's so, so, so tight.

I'd like to take a quick break to acknowledge our sponsor Element Element is an electrolyte drink that has everything you need and Nothing you don't. That means zero sugar and the appropriate ratios of the electrolyte, sodium, magnesium and potassium. And that correct ratio of electrolytes is extremely important because every cell in your body, but especially your nerve cells, your neurons, relies on electrolytes in order to function properly. So when you're well hydrated and you have the appropriate amount of electrolytes in your system, your mental functioning and your physical functioning is improved. I drink one packet of element dissolved in about 16-32oz of water when I wake up in the morning as well as while I exercise. And if I've sweat a lot during that exercise exercise, I often will drink a third element packet dissolved in about 32 ounces of water after I exercise. Element comes in a variety of different flavors, all of which I find really tasty. I like the citrus, I like the watermelon, I like the raspberry. Frankly, I can't pick just one. It also comes in chocolate and chocolate mint, which I find tastes best if they are put into water, dissolved and then heated up. I tend to do that in the winter months because of course you don't just need hydration on hot days and in the summer and spring months, but also in the winter when the temperatures are cold and the environment tends to be dry. If you'd like to try element, you can go to drinklement spelled lmnt.com huberman to try a free sample pack. Again, that's drinkelement.com huberman One thing that I hope people are taking away from this study is that imagine you're somebody who has a very sensitive circadian mood system. Well, that would mean you need less daytime light exposure to feel good or less bad. But it also means that you might need very little light at night in order to negatively impact your mood systems. And in fact they make this argument in the discussion as an interesting point that I think is worth mentioning the way but because here again what I like about this study is that they've separated day and nighttime light exposure. Turns out that many of the drugs that are used to treat bipolar disorder reduce the sense are effective perhaps in part because they reduce the sensitivity of the light sensing circadian apparati. Now that's interesting, right? If you think about this, okay, so these are drugs that can ameliorate some of the symptoms of bipolar, perhaps in part by reducing the extent to which nighttime light exposure can relieve bipolar symptoms. Excuse me, can exacerbate bipolar symptoms. Conversely, there's evidence that people who take certain antidepressants May suppress the ability for daytime light to positively impact the mood systems of the brain. Now, of course, we don't want people halting their medication on the basis of that statement alone. Please don't, you know, talk to your psychiatrist. But if we know one thing for sure, it's that if you want a significant outcome and a paper as a scientist, give a drug, any drug, and look at the amount of rapid eye movement, sleep, or the circadian cycle. Pretty much any drug alters the circadian rhythm, for better or worse. But if we start to think about which medications might adjust our overall sensitivity to light, sometimes this could be a good thing. You think less sensitivity to light. Well, for people who have bipolar disorder, the amount of daytime light exposure isn't that important for their overall mood regulation, but the amount of nighttime light exposure really is. In other words, darkness for eight hours every night should be viewed, in my opinion, as a treatment for bipolar disorder. Not the only treatment. But it's also clear that we should all be avoiding really bright, extensive, really bright nighttime light exposure. I mean, if anything, you know, my takeaway from this study is that darkness at night is the fourth key light stimulus. Now, a couple of things. Very bright moonlight, very bright candlelight is probably only like, gosh, 3 to 50 lux.

What?

When you go outside on a brightly lit full moon night, I encourage people to download this free app. I have no relationship to it called light meter. And it gives you a pretty good read of what the lux are in that environment. By the way, a lot of people don't realize this. They think you just tap the button and then it tells you how many lux you hold it down. It's kind of fun. You can scan around the room and see how many lux are on average coming from that location or outside. Go out on a really bright moonlit night.

I mean, we. We should have a full moon tonight.

Yeah, let's do it. You're not going to get above 100 lux.

That's incredible.

You're sitting at a candlelight dinner with, with your spouse or with friends, and it's clearly bright enough to see them put that lux meter right up. Not too close to the flame. 50 to 200 lux.

I had an interesting experience a couple of months ago on an elk hunt where it was a full moon, which actually makes the hunting not so great. But it was the first time I've ever noticed my shadow in relation to the moon. That's how bright it seemed the light was.

This is Halloween appropriate. Since we're coming up, we're recording this close to Halloween.

It's remarkable. Super interesting to think it could be.

That dim campfire, you know, and firelight, you think? Okay, gathering around a campfire then. Okay. You know, everyone's circadian rhythm must have been disrupted for ages before the development of electricity. No, no, those campfires are extremely bright, but they're not, they're not that bright compared to a very densely overcast day.

And what is your phone if you don't use any sort of light mitigating tech on it?

Well, distance matters.

At the distance we're holding it.

Yeah. So with all the wavelengths cranked up, so. No, there is a nice feature intrinsic to the phone where you can eliminate the blues at night or this kind of thing. But if you crank it up to maximum light intensity, probably something like 500 to 1000 lux. Now keep in mind though, though it's additive, right? So it's over time. So lux is a measure of, I think it relates back to candelas is the amount of light shown at, I think it's like the one meter away and there's a squaring and a falling off of distance. We can look it up. These are old measurement, old school measurements converted to lux. But keep in mind that if you're looking at your phone or tablet at 800 lux or 500 lux in the evening, you do that for two hours. Well, you're summing quite a lot of photons. Now it is true and I do want to be fair to the biology and it'd be dishonest to say anything different. We've hammered on people about not shifting their circadian rhythm with light at night. But we know that the middle of the day, in the middle of the night are circadian dead zones. You can't shift your circadian rhythm that well in the middle of the day, in the middle of the night. But you can provide a wake up signal for your body and brain. It's really that sunrise and sunset that are critical. That's why I said there are four things. See, sunrise or sunrising, you don't need to see across the horizon. Sunset, bright light during the day minimize light exposure at night. And you don't need pitch black. In fact, pitch black probably just increases the frequency of injury. You know, I get up in the middle of the night to use the bathroom probably once I think it's normal, I go back to sleep. You know, if it were pitch black, I'd probably injure myself. So just, just dim it down. Some people use red lights. You know, our friend Rick Rubin, our mutual friend. Yeah, Rick Rubin is.

Can we tell a funny story about Rick?

Yeah, of course. Of course.

You know this story. But just in case Rick's listening, he'll appreciate this. When Rick was here staying last summer, he's up in our guest house and he came down after the first night and he was like, unacceptable. You know what I'm talking about?

Unacceptable accommodations.

What did he do?

He removed all the lighting that existed in that room and replaced it with red light bulbs, which I later used when I stayed here and then later stole when I left. The teenage me, I took him. I took him. That's why Derek, when he stayed here. Elaine, anyone else stayed here? Conti or anyone else didn't have those. I took them. I love them.

So funny. Jill is like, you know, Rick changed every light in the guest house to red. I'm like, yeah, no, I didn't know that. But I'm not surprised.

Yeah, well, in his place, he has mostly either no lighting or red lighting. So during the day he just goes by ambient light and then red light in the evening and. Or candlelight, and it's great. And you know, people hear red lights and they think they have to buy these expensive red light units. That's not what we're talking about. You can literally buy red party lights or just a red bulb. Some people say, well, can I just use a red film or can I put a T shirt over the lamp? I worry about people putting T shirts over lamps because of the fire hazard, but I'll be honest, I dim the lights in my home at night. When I travel, sometimes I will bring one of the stolen from Rick Rubin red lights.

The Rick Rubin stash. Here's something where I've sort of softened my tune. So I used to be kind of a hardliner. No blue light in the evening guy, you know, had the, you know, everything was red light at night. As far as my phone using flux on the computer, you know, whatever it was, I suspect that that matters somewhat. But I think what matters more is the stimulation that may come from those things. And what I've come to realize, at least in me, which means it probably is true in others as well, and at least some others, is that what I'm doing on my phone matters more than how bright my phone is. In other words, if I've got the best blue light filter in the world on my phone, but I'm doom scrolling social media and getting lit up on email, that's way worse for me than if I've got my phone on Maximum light. And I'm like watching YouTube videos of F1 cars and driving around having fun. Like. Yeah, it's a totally different experience. So, so the context matters. And I think, I think for that reason I, I would want people to be mindful of the whole picture. You know, going to bed under a period of, you know, intense duress brought on by something, you know, that's an equally dangerous component to all of this. That's, that's distinct from what we're talking about. But, but you know, you just want to, I'd like, I want people to be able to think of this in the context of everything.

Yeah, I, it's a really important point. You know, one thing I'll say is that if you're going to stay up past your normal bedtime, if you're going to get a lot of light in your eyes, I would hope that it will be for fun reasons and for reasons you enjoy. You should definitely spend some nights out. You should definitely do some all nighters studying. If you really, you know, if you, if it's going to help you get the grade, that's permanent. Right? I'd certainly have done all nighters studying and grant writing for years. You know, there are going to be the inevitable all nighters due to, God forbid, a trip to the hospital or you heard something on the news that really amped you up or you just simply can't sleep. That stuff is going to happen. So I think the goal should be to minimize light exposure at night. And I think what you just said is especially true because we don't know, for instance, people talk about the negative impact of social media. Is it the fact that people are looking at this little box for so many hours per day? Is it all the things they're not doing? Is it what they're looking at per se? All of those things interact and are really important. We know, based on studies from the Stanford Sleep Lab that if you wake up in the middle of the night, looking at what time it is can be very disruptive to your ability to fall back asleep and to your sense the next day. It's a placebo effect, but it's a powerful one of how tired you are the next day. They've done this where they wake people up in the middle of the night and then they say it's 4am versus 2am versus 6am and people's perceived levels of energy during the day in some ways correlate with what they think, how much sleep they think they got. Likewise, and this is one of the Concerns, potential concerns with sleep trackers. Ali Crum talked about this when she came on our podcast. You know, if people see a poor sleep score, they often feel worse than if they see a good sleep score. Now, of course, physiology matters. You can't lie to yourself and say, you know, got a great night's sleep simply by virtue of a sleep score. But I worry more about the false. Well, I don't if it's a false negative, that we don't want to put valence on this. Seeing a bad sleep score and then deciding that you're going to have a terrible day, you know, I think a bad sleep score is an indication that you might need to dial some things in a bit better. Getting a great sleep score is an indication that you might be doing a number of things right and start looking at these things as averages. Wouldn't you. Would you agree?

Yeah, completely. I don't think it's that different from cgm. Right. Like, I think that CGM is an amazing tool to provide insight and you pretty much know the insights after a relatively short period of time, 30 days, maybe at the outside 90 for, for a, really, for a person with a very complicated life and, you know, all you need to know about how the inputs affect the output thereafter, if you choose to use it, it's a behavioral tool. In other words, you're using this to build in a Hawthorne effect. I think the same is largely true with sleep trackers. Most people have this profound sense of learning when they first encounter one of these things. And it's again, you've heard it all 100 times. Oh, my God, I can't believe what alcohol does to my sleep or caloric trackers. Exactly.

Like I think Lane Norton's app Carbon, I have no financial relationship to it. I use it and it's taught me, wow, like, I consume a lot of calories in the form of certain things at certain times of day and there's just a lot of good learning in that.

But it's the act of tracking that helps you manage it. And similarly, I think, think it's the act of knowing you're going to be looking at that score that gamifies it that kind of helps people do the right things. Oh, you know what? I'm not going to have that drink tonight or I'm not going to eat that snack before bed because I've now been conditioned to see how that impacts score. That said, I think that, you know, recovery scores and things like that are just notoriously poor at predicting performance. And I think there's a reason that serious athletes would never use things like that. They would tend to rely on the more tried and true methods of predicting behavior such as heart rate, maybe heart rate variability, but morning resting heart rate, probably more predictive than anything else. And then you know, in workout things such as heart rate, heart rate, recovery, lactate threshold, things like that. So yeah, I agree. I think we have to. And I say this as a guy who's generally perceived to be the most pro device guy in the world. People would be surprised how sparingly I use things like that.

I mean, I do some tracking. Not as much as you. I love things that seem to work the first time and every time. In terms of our natural biology, based on a couple of criteria, there's an established mechanism, it's been explored in the context of pathology, like mental health disorders as well as pro health in healthy individuals that it make really good sense at the level of kind of wellness and let's just say ancient health. You know, when you're talking about getting a lot of sunlight during the day, a lot of people will say, well of course, get outside and play. Not getting too much light at night, of course. This is just good old quote unquote, good old fashioned advice. People spend 90% of their time indoors now. Their daytime environments are too dim, their nighttime environments are too bright. And this kind of misleading aspect of artificial light that when you see a bright bulb, you think I'm getting a lot of photons is part of the problem. And the fact that when you're out on an overcast day and it, you know, you think the sun, quote unquote isn't out, well, it's hidden by cloud cover. But just think about how well you can navigate that environment without a flashlight versus at night where you would require a flashlight. We evolved under this dramatic difference in day, night availability of photons independent whether or not you can quote, see the sun. And it's just very clear that all the mechanisms in our brain and body that regulate mood are just powerfully regulated by this stuff. So I've made it a point to really reduce the amount of nighttime light that I'm getting. But I am less concerned about flipping on the light switch to use use the bathroom as I used to be. I used to think, oh, I'm like quashing all my melatonin. This is terrible. I know I can't shift my circadian clock. Then I know that that light, yes, while it's bright, if it's brief, I'm not going to worry about it too much. Would it be better to have a, you know, dim light on as opposed to a bright light? Sure, but I'm not going to stress it in a hotel bathroom or something. I'm not going to walk around, you know, shielding my eyes. People sometimes ask me, by the way, is it different to look at the phone directly versus if you tilt the phone away? Well, it absolutely is. I mean, think about a flashlight shown on the ground in front of you, very few photons getting in your eyes versus shown directly into your eyes. Think about ambient light from the sun going everywhere versus looking in the general direction of the sun. So east in the morning, west in the afternoon. Of course, the directionality of the light matters. So I'm not saying it, you know, that you need to like peek at your phone as if you're looking, you know, over the edge of a bowl or something into it. But my friend Samur Hataru is head of the Chronic at the National Institutes of Mental Health. We used to room together at meetings. We stopped because he's a terrible snorer. So I just could. There were a few times when I considered suffocating him in the middle of the night since he was already suffocating himself. Now we just, we don't stay in the same rooms anymore. We're no longer postdocs. But I caught him looking at his phone in the middle of the night and he would tilt it like away like he's holding a platter. For those that are just listening and kind of like looking over at the screen there, I'm like, what are you doing? This is ridiculous. Listening. So I'm trying not to get so much light in my eyes. That's a little extreme, but I think it illustrates the point, which is how much direct light exposure you get at night matters, how much direct sunlight exposure you get, especially early in late, early morning, late afternoon and throughout the day. It really matters.

Now remind me, Andrew, what is the wavelength of sunlight?

Great. So sunlight is going to include all visible.

Visible, which runs from how many?

Yeah, so. Well, let's, let's. We can answer two questions there. This wrist sensor detected 470 degree 70 nanometer to 650 nanometer light. So that's going to be blue and ultraviolet. Ultraviolet's kind of.

Yeah, that's kind of like blue to orange.

Yeah, blue. Blue to orange. That's what this was measuring. So red light is going to be more like 680 far red is getting out to 7, 720 and up upwards of that. Blue light is Going to fall somewhere in the, you know, low fours. Ultraviolet is getting down into the high threes and lower. And so these spectra of light. So during the day, you know, midday light, you're getting what looks like white light. You'll see, oh, the sky is blue and the sun is bright white light. It's not even yellow to your eye. And of course, don't stare at it. Especially in the middle of the day, you're getting all visible spectra. So you're getting everything from UV all the way out to red light. It's just coming in at equal intensities.

So is that a potential limitation of this study in that it didn't have a sensor that could pick up up the full spectrum of light?

Potentially, especially since they're, you know, we don't think of humans as UV capable. Like we can't perceive UV light. Like a, a ground squirrel, for instance, can has UV sensors in its eyes. Turns out, you know, why they use this? It's crazy. They actually, you know, when the ground squirrels sit up on their haunches, they're actually signaling one another. They rub urine on their belly and it reflects uv. The New York Times, for some reason has been running a series of papers or articles rather, about naturally occurring fluorescence at night and all sorts of scorpions and monotremes like the platypus. No one really knows the reason for these odd, odd wavelength of light emissions for all these animals. But, you know, we view things in the blue, violet and up to red. And you know, we're not pit vipers. We can't see far red, but we can see lower than 470nm and we can see 7, 650.

Is there a technology reason why they had such a narrow band in these sensors? Is it not possible that they could have used a wrist sensor that was wider?

This study was initiated in 2013. The tech was probably far worse than it is now. Again, I would love for somebody to design an eyeglass where it's measuring how many photons you're getting across the day. I'm not a big fan of having everything be apified, so I would love it if the frame would just shift color across the morning like you go outside on a cloudy day. You know, you wear these glasses and, and by the way, it's fine to wear eyeglasses or contacts for sunlight viewing, for setting your circadian rhythm. People always say, well, why is that okay? And a window is not. Well, corrective lenses are actually focusing the light onto your retina. The windows and and windshields are scattering the light and filtering.

And how much are sunglasses filtering this out?

Way too much. We can safely say way too much, probably causing a tenfold decrement in the total lux count that's landing on your retina. But of course, you know, sunglasses are important. Driving in the. Into sun and, and some people have very sensitive eyes. I can't sit at a cafe with a bright, brightly reflective table in the afternoon. I just, I just squint like crazy. I can't do it. My dad, who's, you know, darker eyed and, you know, he's South, South American descent, he, you know, he can just sit there just fine. My mom, who's got light eyes like me, you know, we're like, oh, it's really tough. You just have a terrible time. You know, people differ in their light sensitivity.

So there's one other macro question I have here, and it's not answerable because without randomization, we can't know it. But it's the question of how much reverse causality can exist in these observations. So again, these observations demonstrate very tight correlations, very strong associations, especially in the five areas that we highlighted. But it's possible that part of what we're seeing is reverse causality brought on by both the treatments, which you've already kind of alluded to, and also the condition itself.

Do you want to explain reverse causality for people? And maybe could you mention for those that missed just the Hawthorne effect?

Just as you. Yeah, yeah, the, the Hawthorne effect is, is an effect that is named after, you know, an observation of what took place in a factory where they were actually studying worker productivity with light, of all things. But what it refers to is the idea that people will change their behavior when they are observed. So if, if I said, well, I really want to know what a day in the life is like for Andrew Huberman, I'm going to follow him around for a day. It's very unlikely that his behavior that day will be exactly as it was if I wasn't there.

And so the reason why you probably will never see A Day in the life of Andrew Huberman, although it's pretty, it's pretty scripted, unless I'm traveling. It's a, it's a, you know, it's morning sunlight, hydration, and, you know, some cardio or weight training and then a lot of time reading papers. It'd be the most boring video in the world because it's mostly me reading and underlining things.

But it's why gamifying things can be beneficial. Right? It's why a CGM can, can be beneficial because it's sort of like somebody's watching you and you're going to modify what you eat in response to it. Or why tracking can really be an effective way to reduce input because you, there's a sense of being monitored by doing that, especially if someone literally monitors it. In other words, you can set up an accountability partner where your health coach or someone is actually seeing the data. So that's what it is. Now as far as reverse causality, when you look at variables, so let's just pick a common one that's unrelated to this. So there's an association that more diet soda consumption is associated with greater obesity. It's a bit paradoxical, right?

Is that true?

It is, yeah. It's. It's been demonstrated in many series that the, the greater the consumption of diet soda, the greater the prevalence of obesity. And that has been postulated by some to suggest that non nutritive sweeteners such as aspartame or sucralose or things like that are actually part of what's causing obesity. And while there are probably some arguments you could make around the impact that those things might have on the gut microbiome and maybe there's some way and that's happening thing, it's also equally likely, if not probably more likely, that there's reverse causality there. That a person who is obese is therefore contemplating how much they're eating or thinking, hey, what's an easy way that I can reduce calories? How about instead of drinking a Coke, I drink a Diet Coke? And so there the causality which you would impute to mean the drink is causing the obesity? It might be. No, the obesity is causing the choice of drinking. So here the question is how much of the effect we're seeing is a result of the condition that's being studied? Right. How much of the disruption in both day and night light exposure is the result of the depression? It's dysregulating the sleep. Maybe they're sleeping more during the day and more awake at night because of depression. Again, these are, you can't know this. This is where epidemiology never allows us to this to determine this. And sadly these questions can only be answered through either direct randomization or Mendelian randomization. Which by the way, I was going to also ask you, do you know if anyone has examined this from a Mendelian standpoint? That would be, that would be very interesting because I have to believe. Well, it would be interesting. I don't know enough about the biology to know what snips would be studyable. But that would be interesting. Interesting.

What Peter is saying is, you know, if you knew something about the genomes of these people, you would be in a great position to perhaps even link up light susceptibility genes or light sensitivity genes with genes for, you know, pathways involved in major depression, bipolar. I mean, getting to this issue of reverse causality, I mean, I think it's very straightforward to imagine that the person who's experiencing a manic episode is going to be up, up for two weeks at a time, sadly, and getting a lot of nighttime light exposure. You know. Now dark, nighttime dark exposure as a treatment for bipolar is something that people are starting to talk about. So making sure that even those people are awake, that they're at least blue, blocking at night, reducing their online activities. But people with severe manic episodes have a hard time regulating their own behavior, of course.

And it's not one or the other. Like I don't want the question to come across to the listener that it has to be one or the other. It's only A can cause B or B can cause A. No, it's actually a lot of times these things feed off each other. Going back to the soda example, I actually think there's a bit of both. Right. I actually think there's a real clear body habitus dictates beverage choice. But I also am starting to think that in susceptible individuals non nutritive sweeteners will alter the gut biome and that alters metabolism.

What about just hunger? I remember Lane telling me, and I've seen at least one of the studies, that water is probably better for us than diet soda, but that for some people diet soda is a great tool for reducing caloric intake. I also know some individuals, not me, who drink diet soda. I drink diet soda from time to time, mainly stevia sweetened sodas. But. But what I'm referring to here are people besides myself who drink diet soda and it seems to stimulate their appetite. There's something about the perception of sweet as driving hunger, whereas not eating or drinking anything with any sweetness doesn't seem to. This is one of the things I wonder if it impacts why some people like intermittent fasting. Because for some people, you know, just even the perception. I wonder if the perception of sweetness or even just the smell of food we know can stimulate appetite. So you can imagine the perception of sweetness in the mouth even if there's no calories there. I don't think it necessarily makes people hypoglycemic but perhaps it makes them think about like sweet means food. For instance, for years I love the combination of a Diet Coke and a slice of pizza whenever I was in New York, ideally two slices of pizza. So now every time I have a Diet Coke, which isn't that often, but I like Diet Coke, especially with a little bit of lemon in it, I just think about a slice of cheese or mushroom or pepperoni pizza. It's like I want it, I crave it more. So there's a paired association there that I think is real. And we know based on Dana Smalls lab at Yale that there's this paired association between the sweetness from sucralose and that there's an insulin response. They actually had to cease the study in kids because they were, they were becoming pre diabetic, you know, which unfortunately meant the study was never published. Have you talked to Dana on this podcast?

No, we, we wrote a premium newsletter on this, this several months ago. It, it's got to be like I don't know, 10 to 20,000 words on all things related to sugar substitutes.

I'll read that.

So, so yeah, folks who are interested in this topic, I would refer them to the premium newsletter on sugar substitutes. I think it was our September edition. The short of it is the data are a little bit noisy but, but there is indeed some, some sweeteners in some studies do result in that phenomenon. You described the cephalic insulin response and I came away from the research that went into that, which was herculean effort on the part of the team, a little bit more confused than when I went in, but being even more cautious around artificial sweeteners than I was going to in so, and not for the reasons that I don't necessarily, I don't. I didn't find any evidence that these things are cancer causing. Right. So that's the headline stuff people worry about oh as like like 10 grams like crazy. I came away more confident that from a, from a long term safety perspective in terms of, in terms of you know, cancer and catastrophic outcomes like that, that wasn't the issue. But I came away much more cautious around these things. Can really be mucking around with both your brain chemistry and your gut chemistry which can pertain to your metabolism. And therefore my takeaway was buyer beware, use limited amounts only. The one by the way, that still emerged to me as a reasonable one. It's the only one that I use and I've talked about it a lot is xylitol. Xylitol is The. Pardon me, I shouldn't say that. Xylitol for chewing. So for gum, and allulose as an additive. So those were the safer. Yes, those are basically the only two I will consume.

I'll drink a Diet Coke every now and again if I'm on a plane or something. You know this law that got passed few years ago that you couldn't bring liquids of your own into the airport and onto the plane.

Like, what a great few years ago.

What a great scheme. What a great scheme to get people to buy overpriced fluids in the airport. Like, I mean, there are more important issues in the world, but, like, this one really gets me. But, yeah, I use a little bit. I drink things with a little bit of stevia in it, the occasional Diet Coke. And I generally avoid sucralose. I don't like the way it tastes. Monk Fruit's too sweet. But, yeah, maybe we'll do a podcast on that in the future. Okay, so I think we can wrap this paper because I really well.

But tell me what you think about that point, Andrew. Like, how. I mean, you know, you know more about this stuff than I do. But. But if you had to just lay on your judgment. Right. So. So if it were. If it were 100 to 0, you would say the light is 100% causal in the effects we're seeing. If it were 0 to 100, you'd say, nope, the behavior is 100% causal of the exposure to light.

Where do you.

Again, you can't know it. What does your intuition tell you?

Okay, there's my intuition and then there's my recognition of my own bias because, you know, I started working on these circadian pathways originating in the eye back in the year in 98 as a graduate student at Berkeley. The cells, these melanopsin intrinsically sensitive retinal ganglion cells, were discovered in the early 2000s by a guy named Iggy Provencio, Dave Burson, Samara Hatar, Sachin Panta, and others. And it was like, one of the most important discoveries in all of biology, clearly. So I've been very excited about these systems, but if I set that aside, so. So biased disclosure made, I think 65 to 75% of the effects are likely due to light directly. Now, it's impossible to tease those apart, as you mentioned, but to play devil's advocate against myself, you know, you could imagine that the depressed individual is laying around indoors with the curtains drawn. They didn't sleep well the night before, which gives you a photosensitivity that Isn't pleasant. Like, like it sucks to have bright light in your eyes first thing in the morning, especially if you didn't sleep well. And then they're making their coffee in a dimly lit, what they think is brightly lit environment and then they're looking at their phone and the state of the world sucks and their state of their internal landscape is rough and maybe they're dealing with a pain or injury or something and their likelihood of getting outside is low. And when they do get outside, they're going to shuffle and not so I could see how the behaviors could really limit the amount of light exposure. And then evening rolls around. They've been tired all day. And a common symptom of depression, you fall asleep and then two or three in the morning, they're wide awake. What are you going to do at two or three when you're wide awake? Sit in the dark? No, you're going to get online, you're going to listen to things you might have. I'm not recommending this, but an alcoholic drink in order to try and fall asleep. I mean, this is the pattern. And so shaking up that pattern is really what so much of my, my public health work these days is about and trying to get people onto a more natural daylight, night, night, dark rhythm. But yeah, it's impossible to tease apart. We do know this, and this is really serious. We know that in almost every instance, almost every psychopathology report of suicide in the weeks, but especially in the days preceding suicide, that person's circadian rhythms look, looked almost inverted from their normal patterns. And that's true of non bipolar individuals as well. You know, circadian disruption and disruption in psychiatric health are inextricable. Conversely, positive mood and affect and circadian behavior seem very correlated. I mean, I think it's clear that if you want to become an early riser, get light in your eyes and get activity in your body early in the day, day, you entrain to those rhythms so that you start to anticipate that morning workout, you start to anticipate the morning sunlight. Just one more scientific point. We know that when you view bright, bright sunlight in the morning, or just sunlight that's illuminating your environment, as you said, you don't even have to see the sun itself, that there's a 55,0% increase in the amplitude of the morning cortisol spike, which is a good thing, right? That's when you want it because it's inversely, the amplitude of the morning cortisol spike is inversely related to the amplitude of the evening Cortisol spike high evening cortisol is associated with middle of the night waking and on and on. So you know, I'm very bullish on these mechanisms. I also love that they're so deeply woven into our evolutionary history, you know, that we share with single cell organisms. It's so wild. But of course there's going to be a bidirectionality there and it's impossible to see where one thing starts and the other one stops.

I mean here's my take. Andrew. First of all, I actually, with far less authority than you agree with your assessment and might even be a little bit more bullish, might even put it at 8020. And here I'll give you my explanations which stem more from my fastidious battles with epidemiology in general. Right. Like because so much of the world that I live in still has to rely on epidemiologic data. And so how do you make sense of it? And the truth of it is most of it is really pretty bad. But I tend to find myself looking at the Austin Bradford Hill criteria all the time. And for folks who don't know, he was a statistician who basically proposed a set of criteria, believe there are eight of them. And I can't believe I don't know every one of them off by heart. I certainly used to. But the more of these criteria that are met within your correlations, the more likelihood you will find causality. So when I think of your data here, the data in this paper, I'll tell you what makes these correlations seem to have causality within them in the direction that's being proposed. Look at the dose effect. So dose effect matters. And this is done in quartiles and that's a very elegant thing. If they just did it as on off, it would be harder.

High, low.

That's right. But the fact that they did in quartiles allows you to see that every example in Figure 2. I don't believe there is an exception to this.

No. And I think also in the, in the.

There's only, there's only one exception to what I'm about to say. Sorry, two out of like God knows how many, they're all monotonically increasing and decreasing. In other words, the dose effect is always present. Another thing is biologic plausibility. You spoken at length about that today. So in other words, sometimes you have to look at epidemiology and ask is there a biologic explanation? And here there is, you've added another one, which is evolutionary conservation observation. To the biologic plausibility, then you can talk about animal models or experiments in humans over short durations that generally support these findings. And so those are just a couple of the, the Bradford Hill criteria that, that lead to, you know, my belief that, yeah, there's reverse causality here, but it's not the full explanation and that more of the explanation is probably the direction that's being proposed. And if that's true, because then at the end of the day, like, what's the purpose of the discussion? The purpose of the discussion is if you are under the influence of any of these psychiatric conditions, in addition to the treatments you're doing now, what else can you do? And to me, the takeaway is follow these light behaviors. I mean, it's, it's, it's a, that's a relatively low lift when you consider some of the other things. Like I'm over here asking people to do zone two for three hours a week and VO2 max work and, and all this other stuff. And like, I think all those things matter for mental health as much as physical health. But this strikes me as on the spectrum of low asks if it shows, if it's only even 30% causality, 70% reverse causality, like, I'll take those. I would still instate that.

Yeah. And it's, you know, it's taking your coffee on the balcony. It's. And people will often say, well, how do you do this with kids? Kids. The kids should be doing it too, right? You know, it means popping your sunglasses off. It means getting out for just a few minutes. And the fact that it's additive, that these, you know, these photon mechanism, photon counting mechanisms, they sum is great. And look, this paper also says, and I should have stated this earlier, if you missed your daytime light ration, get your nighttime dark ration. They are independent and additive. So that's, I mean, that's really something. But of course, ideally you get both. But I appreciate your take on it and, you know, and thanks for, for your expertise in parsing epidemiology. I look at fewer studies of that, of that sort, but I learned from you. And that's one of the reasons I love doing these journal clubs is I learn. So along those lines, tell us about the paper you selected. I'm really eager to learn more.

More. Well, I wanted to pick a paper that was, you know, kind of interesting as a paper. And, and this, this paper, I think is interesting in that it is kind of the landmark study of a class of drugs. But in the same way that you kind of picked a paper that I think has a much broader, overarching importance. The reason I picked this paper, which is from New England Journal of medicine, it's about 10 years old, no, correction, 13 years old, is because it is kind of the landmark study in a class of drugs that I believe are the most relevant class of drugs we've seen so far in cancer therapy. And even though the net effect of these drugs has only served to reduce mortality by maybe 8 to 10%, which is not a huge amount count, it's the manner in which they've done it that gives me great hope for the future, even if it's through other means. So I'll take a step back before we go into the paper for, again, just the context and background. So the human immune system is kind of a remarkable thing. It's hard when you're sort of trying to imagine what's the most amazing part of the human system. And maybe it's my bias as well, because just as you spent, you know, your time in the. In the light system and the photosensing system, I spent my time in the immunology world. But it is remarkable to me how our immune systems evolved. And they have this really brutal task, which is how can they be tuned to detect any foreign pathogen that is harmful without knowing a priori what that could be, while at the same. So in other words, how can you tune a system to be so aggressive that it can eradicate any virus or bacteria billions of years into the future without knowing what it's going to be? But at the same time, it has to be so forgiving of the self that it doesn't turn around and attack the self. It's remarkable. And of course, we can always think of the exceptions. There are things called autoimmune conditions. So clearly, the system fails, fails, and the immune system turns around and attacks the self. If you see a person with vitiligo, I have a little bit of vitiligo on my back, a couple of spots. Clearly the immune system is attacking something there and destroying some of the pigment.

I didn't realize vitiligo was autoimmune.

Yeah, if, you know. So there are lots of, you know, more serious autoimmune conditions. Of course, you know, somebody that has lupus or, you know, where the immune system can be attacking the kidney, the immune system can be attacking anywhere. Autoimmune conditions can be deadly, but fortunately, they are very rare. And for the most part, this immune system works remarkably well. So how does it work and why Is it that cancer seems to evade it virtually all of the time? This is the question. Now let's first of all talk about how it works and then when I tell you how it works, you'll say that sounds amazing. Clearly it should be able to destroy cancer. I'm going to simplify it by only talking about one system which is how T cells recognize and get activated, how T cells recognize antigens. So we have something called an antigen. So an antigen is an antibody generating peptide. So it's a, it's a, it's a protein, almost always a protein. They can be carbohyd, but they're almost always proteins and they're very, very small peptides. Like we're talking as little as nine amino acids, maybe up to 20amino acids. So teeny tiny little peptides. But it's amazing that in such a short peptide the body can recognize if that's Andrew or not Andrew. I mean when again think, think about like we talk about proteins in kilodaltons, right? We're talking about proteins in terms of, of thousands of amino acids that make up every protein in your body. And yet if it samples a protein and sees that, hey, this little 9, 10, 15 peptide amino acid is not part of you, I know it's bad and therefore I'm going to generate an immune response to it. So we have what are called antigen presenting cells. You have cells that go around sampling peptides and they will, on these things called MHC class receptors, bring the peptide up to the surface and serve it up to the T cell. There are two types of these. There's MHC Class 1 and MHC Class 2.

I only this is major histocompatibility complex.

That's correct. And we refer to them that way because they did, because of the context in which they were discovered, which was for organ rejection. Rejection. So not surprisingly, when you need to put a kidney into another person, if that kidney is deemed foreign, it will not last long. In the early days of organ transplantation were rife with immediate rejections. And by not, not I mean the immediates are the ABO incompatibilities. But you know, the, the sort of next layer of incompatibility was MHC incompatibility which would lead to, you know, within, within weeks the organ is gone as opposed to within hours. So you have these two classes of mhc, you have class one and class two. Class one is what we call endogenous. So this is basically what happens when a protein or an antigen is coming from inside the cell. So let's consider the flu. So if you get the flu, the influenza virus infects the respiratory epithelium of your, you know, your larynx. And that virus, as you know, folks listening might remember from our days of talking about COVID viruses, can't replicate on their own. What they do is they hijack the replication machinery of the host and they use that either to insert their RNA or DNA to replicate. And in the process, proteins are being made. Well, those proteins are the proteins of the virus, not of us. So some of those peptides get launched onto these MHC Class 1 gloves. Basically the glove comes up to the surface and a T cell iris infects the respiratory epithelium of your, you know, your larynx. And that virus comes along and in the case of MHC Class 1, it's a CD8T cell. These are what are called the killer T cells. Right. As you know, folks listening might remember from our days of talking about COVID viruses. And so this cell comes along and with its T cell receptor, the teeth can't replicate on their own. What they do is they hijack the replication machinery of the host and they use that either to insert their RNA or D cell receptor meets the MHC class I receptor with the antigen in it. And if that's a lock, it realizes that's my target and it begins to replicate and proliferate and target those. And that creates the immune response. And by the way, that's how it works. When you vaccinate somebody, you're basically pre building that thing up.

So would this fall under the adaptive immune response or the innate immune response, DNA to replicate.

And in the process, proteins are being made. Well, those proteins are the proteins of the virus, not of us. So some of those peptides get launched onto These MH class, MHC class 11 glove, basically the glove, this is adaptive. Yep. Innate is just these pure antibody response in the. On the B cell side. I won't get into that for, for love comes up to the surface and a T cell, for the purpose of this discussion, the other example is MHC Class 2 and that's also part of the adaptive system or the innate system, which is more what we call the exogenous form. So these are peptides that are usually coming from outside the cell. So we're going to focus along, in the case of MHC Class 1, it's a CD8T cell. These are what are called the killer T cells. Right. And so this cell comes along and with its T cell receptor, the T cell receptor meets the MHC class 1 receptor with the antigen in it. And if that's a lock, it realizes that's my target. And it is more on the MHC Class 1 because this is peptides that come from inside the cell. Okay so just keep in the back of your mind, if a foreign protein gets presented from inside a cell to outside a cell, the T cells recognize that and they will mount a foreign response. And by the way, that's why we basically can beat any virus. Like if you consider how many gans to replicate and proliferate and target those and that creates the immune response. And by the way, that's how it works. When you vaccinate somebody, you're basically pre building that thing up.

So would this fall under the adaptive immune response or the innate immune response?

Viruses are around us. The fact that we almost never die from a viral infection is a remarkable achievement though. This is adaptive. Yep. Innate is just these pure antibody response in the, on the B cell side. I won't get into that for, for of how well this immune system works.

We're constantly, constant combating these virus constantly.

And by the way, we don't really have very effective antiviral agents. It's not like antibiotics, like we have antibiotics up the wazoo. I mean we're way better at fighting viruses than bacteria.

Can I just one question. I've always wondered about this. To what extent is our ability to ward off viruses on a day to day basis as an adult reliant on us having been exposed to that virus during development?

For the purpose of this discussion, the other example is MHC Class 2 and that's also part of the adaptive system or the innate system which is more what we call the exogenous form. So these are pept like, like as.

I walk around today, maybe I'll be exposed to a hundred thousand different viruses. Would you say that half of those I've already got antibodies too? Because I, I was exposed to them.

At times that are usually coming from outside the cell. So we're going to focus some prior.

Portion of my life.

Yeah, hard, hard to quantify.

And the other ones I just building up antibodies like it was on, I was on a plane less, more on.

The MHC Class 1 because this is peptides that come from inside the cell. Okay so just keep in the back of your mind if a foreign protein gets presented from inside a cell to outside a cell, the T cells recognize that and they will mount a foreign response. And by the way that's why we basically can beat any virus like if you consider how many of night someone.

Was coughing, so I was hot dieting. I had Covid a little while ago, so I wasn't too worried about that. And I feel great today. But you know, I just assume that on that plane I'm in a swamp of viruses no matter what, and that most of them I've already been exposed to since I was a little kid. So I've got all the antibodies and they're just fighting it back, binding up those viruses and destroying them.

Viruses are around us. The fact that we almost never die from a viral infection is a remarkable achievement. Movement of how well this immune system works.

We're constantly combating these viruses, constantly.

And by the way, we don't really have very effective antiviral agents. It's not like antibiotics, like we have antibiotics up the wazoo. I mean we're way better at fighting viruses than bacteria.

Can I just.

Yeah, I think it's part that and I also think it's part of them that our body can destroy without mounting much of an immune response. So therefore your immune system is doing the work and it's. Yet it's not mounting a systemic inflammatory response that you're not sensing.

So is it also a physical trapping in, you know, in my nasal epithelium? It's a virus.

Yeah. So, so yeah, like there you have huge barriers, right? So the skin, you know, the hairs in your nose, all of the.

One question I've always wondered about this. To what extent is our ability to ward off viruses on a day to day basis as an adult reliant on us having been exposed to that virus during development? Like, like as I walk around today, maybe I'll be exposed to a hundred thousand different viruses. Viruses. Would you say that half of those I've already got antibodies too? Because I, I was exposed to them.

These things are huge barriers. But assuming that still a bunch of them are getting in, at least the respiratory ones, that's the other thing to keep in mind. Right. There are certain viruses that are totally useless, floating around the air. Right. There are certain viruses, you know, the viruses that most people are really afraid of, you know, hep C, hep B, hiv. Well, you know, if they're sitting on a table or floating around some prior.

Portion of my life.

Yeah, Hard, hard, quantified.

And the other ones, I'm just building up antibodies like it was on. I was on a plane last night, someone was coughing, so I was hiding. I had Covid a little while ago, so I wasn't too worried about that. And I feel great today.

But the air, they're of no threat to you. They have to be, you know, sort of transmitted through the barrier.

You know, I just assume that on that plane I'm in a swamp of viruses no matter what, and that most of them I've already been exposed to.

But again, some of these viruses you're going to defeat with an enormous response. And then some of them, you know, like, why is influenza, quote unquote, such a bad virus? Whereas the common respiratory cold kind of sidelines you for a day. It's the immune response that you're feeling the worse. The bigger the immune response to the virus, the more you're feeling that you feel your immune system going crazy. Right. You know, the interleukins that are spiking.

Since I was a little kid, so I've got all the antibodies and they're just fighting it back, binding up those viruses and. And destroying them.

The third spacing that occurs to get more and more of the immune cells there. The spike of your. Yeah, I think it's part that. And I also think it's part of them that our body can destroy without mounting much of an immune response. So therefore your immune system is doing the work and it's. Yet it's not mounting a systemic inflammatory response that you're not sensing.

So is it also a physical trapping in, you know, in my nasal.

Your temperature as your body basically tries to cook the virus. All of that stuff is your body doing. Yep. Yeah. You're being drained in all this happening. So one more point I'll mention just by, just to close the loop on the autoimmunity. How is it that we learn not to attack ourselves? That's something called thymic selection that occurs in infancy. So you and I have a no good for nothing, tiny little thymus that would be. It's almost impossible to Helium viruses. Yeah. So. So, yeah, like there you have huge barriers, right? So the skin, you know, the hairs in your nose, all of these things are huge barriers. But assuming that still a bunch of them are getting in, at least the respiratory ones, that's the other thing to keep in mind, right. There are certain viruses that are totally useless, floating around the air. Right. There are certain viruses, you know, the viruses that most people are really afraid of, you know, hep C. See these things, you know, when we used to operate on people, you know, the thymus is barely visible in an adult, in a healthy adult, outside of thymic tumors. But as a child, in a child, the thymus is quite large and the purpose of the thymus is to educate T cells and basically show the T cells what self is. And any T cell that doesn't immediately recognize it gets hep B, hiv. Well, you know, if they're sitting on a table or floating around the air, they're of no threat to you. They have to be, you know, sort of transmitted through the barrier kill. So it's a, it's a really clever system where we basically teach you to recognize self there at a very early age. And if you can't do that, you're weeded out. But again, some of these viruses you're going to defeat without an enormous response. And then some of them, you know, like, why is influenza, quote unquote, such a bad virus? Whereas the common respiratory cold and then the thymus involutes thereafter because it's sort of served its purpose. Therapist okay, now let's talk about cancer. So what do we know about cancer? So we know that again, you know, cancer is a genetic disease in the sense that every cancer has genetic mutations. Most of those mutations are somatic, which means most of those mutations are mutate. Kind of sidelines you for a day. It's the immune response that you're feeling the worst. The big patients that occur during the course of our life, they're not germline mutations. You're the immune response months to the virus. The more you're feeling that, you feel your immune system going crazy. Right. You know, the interleukins that are spiking, the third spacing that occurs to get more and more of the immune cells there. The spike of your.

The germline being the eggs and sperm. Right. So it's all other cells. And I love that you pointed out that, you know, there can be genetic, that cancer can be genetic, but isn't necessarily inherited.

Your temperature as your body basically tries to cook the virus, virus, all of that stuff, is it?

Right. In fact, it's really genetic and they think inherited, right?

Yes.

Inherited is always genetic to some extent, but genetic isn't always inherited.

Yeah. So they're your body, the fatigue. Yep. Yeah. You're being drained and all this happening. So one more point I'll mention just. But just to close the loop on the autoimmunity, how is it that we learn not to attack ourselves? That's something called thymic selection that occurs, occurs in infancy. So you and are a handful of cancers that are derived from inherited mutations. So lynch syndrome is an example of that. Hereditary polyposis is an example of that. Where you have a gene that gets passed through the germline. And that gene codes for a protein like all genes do. And it's either you have too much of a gene or too little of a gene. So it's either a gene that promotes cancer. Cancer, and you have too much of that, or it's a gene that prevents cancer and you have too little of it, or a dysfunctional version of it. Right. So brci have a no good for nothing, tiny little thymus that would be. It's almost impossible to see these things. You know, when we used to operate on people, you know, the thymus is barely visible in an adult, in a healthy adult, outside of thymic tumors. But as a child, in a child, the thymus is quite large. And the purpose of the thymus is to educate T cells. And basically, okay, as an example of that, BRCA is hereditary. BRCA codes for a protein. And the. The women and men, but mostly the women that we think about who have a BRCA mutation that all in some cases almost guarantees breast cancer. It's because of a defective copy. So it's like they don't get the protein that they need to protect them from breast cancer. Cancer. So what do we know? Show the T cells what self is, and any T cell that doesn't immediately recognize it gets killed. So it's a really clever system where we basically teach you to recognize self there at a very early age. And if you can't do that, you're weeded out. And then the thymus involutes thereafter because it's sort of. Well, we know that. And this is probably one of the most remarkable things I've ever learned, and it still blows my mind every time. Well, actually, before I get to that point, I want to make. I want to make another point. Okay, so. So you might think so, cancer. We, you know, our cells become cancerous, but they're clearly hijacked because they have these mutations and as a result of these mutations, served its purpose. Okay, now let's talk about cancer. So what do we know about cancer? Cancer? So we know that again, you know, cancer is a genetic disease in the sense that every cancer has genetic mutations. Most of those mutations are somatic, which means most of those mutations are mutates. They make proteins that allow cancers to behave differently. And cancers behave differently from non cancers in two very critical ways. The first way is that they do not respond to cell cycle signals signaling. So if you cut your skin, it heals. But how does it know to heal patients that occur during the course of our life? They're not germline mutations. Well, just. Right. And not to keep growing and growing and growing and growing and growing. Well, it knows that because there are cell cycle signals.

The germline being the eggs and sperm. Right. So it's all other cells. And I love that you pointed out that you know there can be be gen that cancer can be genetic but isn't necessarily inherited. Right. In fact it's really genetic and they think inherited.

Right.

But inherited is always genetic to some extent.

But those that tell it time to grow, time to stop. If believe it or not, this is an extreme example. If you donated to me, half of.

Your genetic isn't always inherited.

Yeah. So they're ever. Which I know you would.

Absolutely. I'd give you more than half of my life.

Well, you don't need to give me.

If it meant that we could keep doing these journal clubs.

Right. Within months you would regenerate a full liver. That's so isn't that are a handful of cancers that are derived from inherited mutations. So lynch syndrome is an example of that. Hereditary polyposis is an example of that. Where you have a gene that gets past Mason.

So. Well, it's like a salamander. You cut off a salamander limb and please don't do that experiment because other people are doing doing it anyway. And it grows back and it knows.

How much to grow back. So. So when the cell is perfectly functioning, it knows how much to grow and. And it's well, cancer lose through the germline. And that gene codes for a protein like all genes do. And it's either you have too much of a genesis, that ability. That is one of the hallmarks of cancer. It just keeps growing. It doesn't grow faster by the way. That's a misnomer. People think cancers grow faster than non cancers. There's no real evidence that that's the case. They just don't stop growing. The second property of cancer is the or too little of the gene. So it's either a gene that promotes cancer and you have too much of that or it's a gene that prevents cancer and you have too little of it. Or a dysfunctional version of it. Right. So BRCA is an example of that. BRCA is hereditary. BRCA codes for a protein and the. The women capacity to leave, leave the site of origin, go someplace else and take up residence.

So that's metastasis.

That's the metastases component. So if you think about it for a minute, a cell that never stops replicating and has the capacity to up and leave and move and take up residence is clearly different from the cell itself. Right. So if I have a cell of colonin and men, but mostly the women that we think about who have a BRCA mutation that all in some cases almost guarantees breast cancer, it's because of a defective CA copy. So it's like they don't get the protein that they need to protect them from breast cancer. So what do we know? Well, we know that, and this is probably one of the most remarkable things I've ever. Epithelium, the cell that lines the inside of my colon, it's clearly got a set of proteins in it. But if all of a sudden that thing can grow, grow, grow, grow, grow, not stop, not stop, not, not listen to the signal and then somehow wind its way into the liver and just keep growing and growing and growing, it must have different proteins. So the question then becomes learned and it still blows my mind every time. Well, actually, why does cancer even exist? How has our immune system not figured out a way to just silence this and eradicate it the way it does to virtually every virus you encounter? Before I get to that point, I want to make, I want to make another point. Okay, so, so you might think so cancer, we, you know, our cells become cancerous, but they're clearly hijacked because they have these mutations. And as a result of these mutations, they make proteins that allow cancers to behave differently. And, and to me, this is one of the most interesting questions in all of biology. And it really comes down to how clever cancer is, unfortunately, how evolutionarily clever it is. It basically does a lot of things, things to trick the answers behave differently from non cancers in two very critical ways. The first way is that they do not respond to cell cycle signaling. So if you cut your skin, it heals. But how does it know to heal immune system? So it has its own secretory factors that tamp down the immune system will just right. And not to keep growing and growing and growing, growing and growing and growing. Well, it knows that because there are cell cycle signals, it grows in an environment because of its nature. So one of the things that's long understood about cancer is it's heavily glycolytic. And when something is heavily glycolytic, it's going glucose to pyruvate to lactate non stop. There are lots of reasons for that that tell it time to grow, time to stop. If believe it or not, this is an extreme example. If you donated to me half of your live, I think there's More than one.

What does that afford? It does that. Well, so it's interesting is that afforded.

A migratory potential, which I know you would.

Absolutely. I'd give you more than half of my.

Well, you don't need to give me.

If it meant that we could keep doing these.

Yeah, no. So it's super interesting. So. So that's the effect that. What I just described is called the Warburg effect. And when Warburg proposed this, which God was probably in the 1920s, it was before within months you would regenerate a full liver.

That's so.

Isn't that before World War I? Before World War II, he proposed it. He thought the mitochondria of cancer cells were defective. So he proposed that the, you know, cancer cells, mitochondria don't work, hence they have to undergo glycolysis. They can't undergo aerobic metabolism. We now know that that's not the case. Amazing.

So, wow. It's like a salamander. You cut off a salamander limb and please don't do that experiment because other people are doing it anyway. And it grows back and it knows.

How much to grow back. So. So when a cell is perfectly functioning, it knows how much to grow and. And it's. Well, cancer lose. So we now know that the. The Warburg effect, or the Warburg effect, if I'll refer to him correctly by his name, uses that ability. That is one of the hallmarks of cancer. It just keeps growing, it doesn't grow fat, almost assuredly does not have to do with defective mitochondria. Others have proposed several mechanisms. I think there's probably more than one thing going on. So. So, so a paper that came out in 2009, very influential paper by a guy named Matt Vanderheiden and Aster, by the way, that's a misnomer. People think cancers grow faster than non cancers. There's no real evidence that that's the case. They just don't stop growing. The second property of cancer is, is the capacity to leave the site of origin, go someplace else and take up resin. Craig Thompson and Luke Cantley proposed that the reason that cancer cells. That's metastasis, that's the metastases component. So if you think about it for a minute, I'll do the Warburg effect is that they're not optimizing for energy, they're optimizing for cellular building blocks. And if you do the mass balance, it completely makes sense. Like dividing cells need building blocks more than energy and glycolysis. While very inefficient for generating ATP is much more. A cell that never stops replicating and has the capacity to up and leave and move and take up residence is clearly different from the cell itself. Right. So if I have a cell of colon efficient at generating substrate to make more cells. But another proposed mechanism is exactly at this one. Glycolysytic epithelium. The cell that lines the inside of my colon, it's clearly got a set of proteins, lowers the surrounding ph because of lactate, lactate attracts hydrogen, PH goes down and guess what that does to the immune system? Detracts the immune system. So it's also a way to hide from the immune system.

So there's a. Like a ph cloaking, leveraging ph to cloak in it.

But if all of a sudden that thing can grow, grow, grow, grow, grow, not stop, not stop.

That's right. The signal that the immune system would.

Otherwise otherwise see, not, not listen to the signal and then somehow wind its way into the liver and just keep growing and growing and growing. It must have different proteins. So the question then becomes, yep. And then when you layer on top of that that it knows how to secrete things like IL10, TGF beta, all of these other. Why does cancer even exist? How has our immune system not figured out a way to just secretory factors that also inhibit the immune system system, basically it's figured out a way to kind of hide itself from the immune system.

The way you describe it, cancer sounds like a virus.

Yes.

I mean it sounds a lot like a virus. And that leads me to ask, are.

There any examples silence this and eradicate it the way it does to virtually.

Every virus you encounter of contagious cancers. I recall seeing some studies about these.

And to me, this is one of the most interesting questions in all of biology. And it really comes down to how, how clever cancer is, unfortunately, how evolutionarily.

Clever little critters down in Australia, Tasmanian devils that like they would. They scratch each other and fight as Tasmanian devils do. They're actually quite cute. And they would get cancers and tumors.

It is, it basically does a lot of things to trick the going on their faces. So, so it's.

And so it was, it was, it was like a literal physical interaction that could transmit cancer from one animal to the next.

So it's less that there are viruses that cause cancer. So in that sense, you could argue, yes, there are contagious cancers. Well, hpv, sure, yeah. Hpv, hep B, hep C. But, but there are even cancers like cutaneous cancers that arise from Viruses by immune system. System. So it has its own secretory factors that tamp down the immune system. But I don't know if that's quite the same as what you're saying. Like.

No, no, it's in. They're both it. What you're saying is an important point. I mean, we don't want to go down the rabbit hole of hpv, but.

Right.

That's.

It grows in an environment because of its nature. So one of the things that's long understood about cancer is it's heavily glycolytic. And when something is heavily glycolytic, it's going.

Increasing susceptibility to cervical cancer. Now there's a vaccine against hpv, right? There wasn't when we were in college, as we all knew, there was no vaccine. But the. Okay, so.

But yeah, glucose to pyruvate, to lactate non stop. There are lots of reasons for that.

Direct transmission of cancers from one one organism to the next.

More rare. Yes, yes. Okay. So now a moment ago I said there's this really incredible thing about cancer that blows my mind. I think there's more than one.

What does that afford it? Well, so it's interesting. Does that afford it a migratory potential?

And about our immune system, which is that at least 80. No. So it's super interesting. So that's the effect. What I just described is called the Warburg effect. And when Warburg proposed this, which God was probably in the 1920s, it was before percent of solid organ tumors. And we're going to mostly talk about solid organ tumors because that's where the field of oncology has made very little progress. So if you go back 50 years, where has oncology made huge progress? It's made great progress in blood tumors, leukemias and some kinds of lymphomas. In fact, there's two kinds of lymphomas where the progress has been remarkable. One has been in. In for World War I, before World War II. He proposed it because he thought Hodgkin's lymphoma. And the other has also been an immunotherapy has been in a type of B cell lymphoma. The mitochondria of cancer cells were defective. So he proposed that the, you know, cancer cells might. Where that B cell demonstrates or presents something called a CD19 receptor. So in, in. In B cell lymphomas with CD19 immunotherapy, there's a very unique niche. Imandria don't work, hence they have to undergo glycolysis. They can't undergo aerobic immunotherapy. We won't talk about that today. Called CAR T therapy. That has got rid of those guys. And then metabolism. We now know that that's not the case. So we now know that the. The Warburg effect or the Warburg effect if I'll refer to him correctly by his name. Leukemia have also been pretty good. But in solid organ tumors there have been only two real breakthroughs in the last 50 years. One has been the therapy for a certain type of testicular cancer. And it's almost assuredly does not have to do with defective mitochondria. Others have proposed several mechanisms. I think really just a chemotherapy cocktail that has been found to work really well. And the other has been in this. I think there's probably more than one thing going on. So. So. So a paper that came out in 2009 very influential paper by a guy named Matt Vanderheiden and really rare kind of gastric cancer called the GI stromal tumor which happens to result. Craig Thompson and Luke Cantley proposed that the reason that cancer cell from one mutation in a K pathway. And there's one drug that can now target that and it works. It's kind of amazing cures that cancer cures that. What I'm talking about out are the cancers that kill virtually everybody else. This is what. When you sort of line up what are the big causes of cancer death. I'll do the Warburg effect is that they're not optimizing for energy. They're optimizing for cellular building blocks. And if you do the mass balance it completely makes sense. Like dividing cells need building blocks more than energy. And glycolysis while very inefficient for generating ATP is much more. Let's start at the top. It's lung. It's then breast and prostate in men and women. It's colorectal. It's pancreas. Those are the big five. They kill more than 50% of Americans. It cancer wise not sorry. Let me restate that. Efficient at generating substrate to make more cells. But another proposed mechanism is exactly at this one glycolysis. More than 50% of cancer deaths in Americans come from those five. These are what we call the solid. Epithelius lowers the surrounding PA because of lactate. Lactate attracts hydrogen. PH goes down and guess what that does to the immune tumors. And you can march down the list. And most cancers that most people are thinking of are those cancers. Well here's the thing. More than 80% of those cancers have antigens that are recognized by the host's immune system. I will state it again because it is so profound, 80% at least of those cancers actually generate an antigen meaning system detracts the immune system. So it's also a way to hide from the immune system.

So there's a like a ph cloaking.

Leveraging ph to cloak a little peptide in that cell gets presented to the T cell and it is recognizable. And now the question is why is that not sufficient to induce the signal.

That the immune system would otherwise.

Yep. And then when you layer on top of that that it knows how to secrete things like IL10, TGF beta, all of these other see remission. And the short answer is there are not enough T cells that are able to act and or they are being sufficiently pretory factors that also inhibit the immune system. Basically it's figured out a way to kind of hide itself from the immune system.

The way you describe it, cancer sounds.

Like a virus virus inhibited from acting. Which gets me to the point of this paper. One of the ways in which the body inhibits the immune system which we should remind ourselves is an important thing. Right. Is something called the check. Yes.

I mean it sounds a lot like a virus. And that leads me to ask are there any examples point inhibitor.

Okay, so go back to that idea that I talked about before.

You have an apples of contagious cancers. I recall seeing some studies about these. These little critters down in Australia, Tasmanian devils that like they would they scratch each other and fight as Tasmanian devils do. They're actually quite cute. And they would get cancers and tumors.

Grow antigen presenting cell. It brings up an MHC receptor with a peptide on it. And there is a T cell that is coming. And I actually brought a diagram which we're going to. I'm going to link to this because I don't want to make this too complicated but I really think that this.

Figure on their face.

Yes. So. So it.

And so it was. It was. It was like a literal physical interaction that could.

Is helpful to understand how these papers how these drugs work. So the MHC transmit cancer from one.

Animal to the next.

So it's less that there are viruses that cause cancer. So in that sense you could argue yes, there are contagious cancers.

Well, hpv, sure.

Yeah. Hpv Hep B, hep C. But. But there even receptor with the peptide is sitting there and it binds to the TC T cell receptor on the T cell. But there is another receptor on the T cell, a CTLA4 receptor. And that binds to a receptor that I won't bother naming now because it's. The names don't matter. But there's another receptor on the antigen presenting cell that binds to. To that and that cancers like cutaneous cancers that arise from viruses. But I don't know if that's quite the same as what you're saying. Like acts as the brakes in the reaction. So CTLA4, which is on the T cell binds to another CD receptor on the antigen presenting cell and it says tamp down the response and no, no, it's in.

They're both. What you're saying is an important point. I mean we don't want to go down the rabbit hole of hpv, but.

Right.

That's increasing susceptibility to cervical cancer. Now there's a vaccine against hpv.

Right?

There wasn't when we were in college.

The reason for that is we want to keep our immune system in check. This basically is a way of asking.

As we all knew, there was no vaccine. But the. Okay, so. But yeah. Direct transmission of cancers from 1.1 organism.

To the next more rare immune system because Right. Remember when the immune system sees that antigen, it wants to go nuts. It wants to start replicating and killing. This is a CD8T cell. It is a targeted killer T cell. The checkpoint says let's double check that. Let's be. Yes. Okay, so now here a moment ago I said there's this really incredible thing about cancer that blows my mind and about our immune system which is that at least 80. Sure, let's tamp down their response. And as a result of that, a thought experiment emerged which was what if we block CTLA 4? What if we block the checkpoint? Could we unleash the immune system a little bit more? 8% of solid organ tumors. And we're going to mostly talk about solid organ tumors because that's where the field and I will say this, at the time it was proposed, it seemed a bit far of oncology has made very little progress. So if you go back 50 years, where has oncology made fetched because of the complexity of the immune system? It seemed a little far fetched that huge progress. It's made great progress in blood tumors, leukemias and some kinds of lymphomas. In fact, there's two kinds of lymphomas where the progress has been remarkable. One has been in. In simply blocking the checkpoint would have any effect. It's also worth noting that prior to this one immunotherapy had found some efficacy which was trying the Exact opposite strategy. Rather than blocking the inhibitor, it was throwing Hodgkin's lymphoma. And the other has also been an immunotherapy, has been in a type of B cell lymphoma where that B cell demonstrates or presents something called a CD19 receptor. So in. In. In B cell lymphomas with CD19 immunotherapy, there's a very unique niche immunotherapy, we won't talk about that today, called CAR T therapy. That has got rid of those guys. And then more accelerant at the fire, which was giving something called Interleukin 2. So Interleukin 2 is, for lack of a better word, candy and fuel for T cell cells. So the idea was, if we have T cells that innately recognize a cancer antigen, can we just give high doses of Interleukin 2 and have them under? Leukemias have also been pretty good. But in solid organ tumors, there have been only two real breakthroughs in the last 50 years. One has been the therapy for a certain type of testicular cancer cancer. And it's really just a chemotherapy cocktail that has been found to work really well. And the other has been in the show proliferation and response. And the answer turned out to be yes, but only in two cancers, melanoma and kidney cancer, and only at very small levels. About 10% of the population would respond to these things. Now, look, that's 10% of people who were going to be dead within six months. Because these are devastating cancers. And once they spread, there are no really rare kind of gastric cancer called the GI stromal tumor tumor, which happens to result from one mutation in a kinase pathway. And there's one drug that can now target that. And it works. It's kind of amazing cures that cancer cures that. What I'm talking about are the cancers that kill virtually everybody else. This is what. When you sort of line up, what are the big causes of cancer death treatments that have any efficacy whatsoever. In fact, I think median survival for metastatic melanoma at the time was probably four months. Months. So this was a very grim death sentence. But the idea now was what about doing the exact opposite approach? Instead of trying to throw more fire at the T cell, what if we can take its breaks down less gas. Pardon me? Instead of giving more gas, let's give less. Let's start at the top. It's lung. It's then breast and prostate. In men and women, it's colorectal, it's pancreas. Those are the big five. Five. They kill more than 50% of Americans. It cancer wise not. Sorry, let me restate that. More than 50% of cancer deaths in Americans come from those five. These are what we call the solid epithelial breaks. And there were some phase two, some phase one studies that demonstrate efficacy. Phase two and the paper I'm going to talk about today is the. Is the phase three study that compared the first version of these. So, so the. The drug we're going to talk about today is an anti CTLA4 drug called tumors. And you can march down the list. And most cancers that most people are thinking of are those cancers. Well, here's the thing. More than 80% of those cancers have antigens that are recognized by the host's immune system. I will state it again because it is so profound. 80% at least of those cancers actually generate an antigen meaning ipilimab. There is another drug out there that came. Came along shortly thereafter that is an anti PD1 drug. So PD1 turns out to be another one of these checkpoints on T. A little peptide in that cell gets presented to the T cell and it is recognizable. And now the question is why is that not sufficient to induce cells. And the Nobel prize by the way, I think it was 2018 or 2019 in medicine or physiology was actually awarded to the two scientists who discovered CTLA 4 and PD1. So you know this. I believe this is the only Nobel prize in medicine for immunotherapy therapy. It's a very big deal. So this study remission and the short answer is there are not enough T cells that are able to act and or they are being sufficiently sought to compare the effect of anti CTLA 4 to a placebo. And the placebo in this case was the inhibitor from acting. Which gets me to the point of this paper. One of the ways in which the body inhibits the immune system which not a real placebo. It was a peptide vaccine called GP100. To ask the question in patients with metastatic melanoma we should remind ourselves is an important thing right. Is something called a checkpoint inhibitor. Okay so go back to that idea that I talked about before. You have an Emma. What would be the impact on median survival and overall survival. So let's talk a little bit about the paper. So again, one of the funny things about this is I used to read these papers a lot, Andrew. These, these used to be. These used to be my bread and butter papers. So I, I mean I, I, you know be, you know reading the antigen presenting cell it brings up an MHC receptor with a peptide on it. And there is a T cell that is coming. And I actually brought a diagram which we're gonna, I'm gonna link to this because I, I don't want to make this too complicated, but I really think that this figure is helpful to understand how these papers, how these drugs work. So the MHC is like, I'm, you know, it's my hobby and, and I don't read them that much anymore. So it was kind of amazing how long it took me to remind myself of stuff I used to remember. But you do have to kind of go back and read the methods and figure out who were the patients in this, what was the eligibility criter with the peptide is sitting there and it binds to the TC T cell receptor on the T cell. But there is another receptor on the T cell, a CTLA4 receptor, and that binds to a receptor that I won't bother naming now because it's. The names don't matter, but there's another receptor on the antigen presenting cell that binds to that and that area. Why did they do it this way? And of course it all kind of came back to me, but it took a minute. So. So the first thing is these are all patients who had progressed through every step standard therapy. So these are patients for whom there were no other options. These patients either acts as the brakes in the reaction. So CTLA 4, which is on the T cell binds to, had very advanced stage three melanoma, which means it was local, regional melanoma, but it couldn't be resected. So an example of that would be, be a cancer that was, you know, completely engulfing, like where, let's say another CD receptor on the antigen presenting cell and it says tamp down the response. And the reason for that is we want to keep our immune system in check. This basically is a way of asking. The primary site was the cheek and it had completely grown into all of the surrounding soft tissue. It had, it hadn't spread anywhere, but it was, you know, all the lymph nodes of the neck. And, and I've seen patients immune system, because remember, when the immune system sees that antigen, it wants to go nuts. It wants to start replicating and killing that. This is a CD8T cell. It's like this and it's, you know, it's just completely disfiguring. And they'd already been through the standard chemotherapy and nothing was working. And the thing was growing. And then it was mostly made up of patients with stage four cancer. Now, melanoma has a very funny staging system, is a targeted killer T cell. The checkpoint says, let's double check that, let's be sure, let's tamp down the response. And as a result of that, a thought experiment emerged which. So in cancer, we typically talk about Something called the TNM staging system is what if we block CTLA 4? What if we block the checkpoint? Could we unleash the immune system a little bit more? Is the standard way that cancers are staged. T refers to the tumor size, N refers to the lymph node status, and M refers to the presence or absence of metastases. And for most cancers, it is a very simple system. It is, you know, T is typically a number 1, 2. And I will say this, at the time it was proposed, it seemed a bit far fetched because of the complexity of the immune system. It seemed a little far fetched that sometimes up to 3 and 4 N is typically 0. Simply blocking the checkpoint would have any effect. It's also worth noting that Prior to this 1, 1 or 2 and M is 0 or 1, either there's no mets or there are mets. So, for example, in colorectal cancer, the T staging determines the depth in the colon wall that it went. N is did it go to mets? And I think in colon, I'm a little rusty on this. I think colon has n 0, 1 or 2, depending on how many lymph nodes. And immunotherapy had found some efficacy, which was trying the exact opposite strategy. Rather than blocking the inhibitor, it was throwing an M0. Did it go to anything beyond that, like to the liver, lung, et cetera, or. No, not more accelerant at the fire, which was giving something called Interleukin 2. So Interleukin 2 is, for lack of a better word, candy and fuel for T cells. So the idea was if we have melanoma is a bit more complicated. It has m0, meaning no mets, but it also has m1a, m1b, m1c, and m1d. And within each of those, it has a threshold for high and low lactate dehydration, hydrogenase, or L T cells that innately recognize a cancer antigen. Can we just give high doses of Interleukin 2 and have them under DH? So it's both a staging based on imaging and biochemical. And the reason for that is LDH level is such a strong prognostic indicator of survival. In addition to M staging, higher LDH levels tend to reflect more acidity, which we talked about. Why that's problematic tends to reflect faster growing tumor proliferation and response. And the answer turned out to be yes, but only in two cancers, melanoma and kidney cancer. And only at very small levels. About 10% of the population would respond to these things. Now look, that's 10% of people who were going to be dead within six months. Because these are devastating cancers. And once they spread, there are no higher turnover, higher metabolic activity. M1A. Let me see if I can remember this. M1A's are cancers that have metastasized to surrounding soft tissue or soft tissue anywhere in the body. So anywhere else on the skin and you might think, well that's kind of crazy. Like how does that happen? And it's really bizarre treatments that have any efficacy whatsoever. In fact, I think median survival for metastatic melanoma at the time was probably four months. So this was a very grim death sentence. But the idea now was what about doing the exact opposite approach? Instead of trying to throw more fire at the T cell, what if we can take its breaks down less gas? Pardon me? Instead of giving more gas, let's give less. You can have a patient who had a melanoma that showed up in one part of their body and then they have metastasis on other parts of their skin. M1B is, and I always get B and C confused. I think B is the lung. So M1B is to the lung, M1C is to any internal organ. So breaks. And there were some phase two, some phase one studies that demonstrated efficacy. Phase two and the paper I'm going to talk about today is the, is the phase three study that compared the first version of these. So, so the, the drug we're going to talk about today is an anti CTLA 4 drug called Liver etc and M1D is to the CNS. And as those numbers increase, as those letters increase, the prognosis gets lower and lower and lower. So one of the first things I always look at when I look at a paper like this is tell me about the patient population. Like what, what was the, you know, what was the breakdown of patients. And in Table 1, so that's again in clinical papers like this, Table 1 is always, always, always baseline characteristics. Oh, I should mention one other thing, Andrew. This was done ipilimab. There is another as a three to one to one randomization. So again, in the simplest form, a study would have two groups, right? You would have, have their drug out there that came, came along shortly thereafter. That is an anti PD1 drug. So PD1 turns out to be another one of these checkpoints on T. We're going to just have a treatment group and a placebo group. But in this arm you had three groups with one of them being the placebo. The placebo got just GP100, which is just a cancer vaccine, by the way. This is a cancer vaccine that never showed any efficacy. So it was a cancer cells. And the Nobel Prize, by the way, I think it was 2018 or 2019 in medicine or physiology was a vaccine that had been tested both with Interleukin 2 directly and actually awarded to the two scientists who discovered CTLA 4 and PD1. So, you know, this, I believe this is the only Nobel Prize in medicine for immunotherapy therapy as an adjuvant for patients who had metastatic melanoma risk or had. Sorry, not. It's a very big deal. So this study, metastatic melanoma, who had melanoma resected, who were tumor free and then given the vaccine as adjuvants to see did that have an effect on outcomes. And it didn't. So it's kind of a known placebo. So you had that group, then you had the anti CTLA 4 group group and then you had anti CTLA 4 plus GP 100. As the rationale for the 3 to 1 to 1. It's basically it increases statistical power. Right. So, you know, this total study was a little under 700. People sought to compare the effect of anti CTLA 4 to a placebo and the placebo in this case was not a real placebo. It was a peptide vaccine called GP100. To ask the question, in patients with metastatic melano, they put 400 in the anti ctla 4 plus gp 100 group and then, you know, a little over 130 in each of the other two groups. So you're always going to be able to make these two comparisons. Right. What you can check by doing this is is there any effective GP100 in this set which had never been done before? What would be the impact on median survival and overall survival? So again, GP100 is a known. So let's talk a little bit about the paper. So again, one of the funny things about this is I used to read these papers a lot, Andrew. These, these used to be, these used to be my bread and butter papers. So I, I mean I, I, you know, be, you know, reading the protein expressed by melanoma and all of these people were haplotyped to make sure that their immune system would recognize it. And the question was, would giving people Anti CTLA 4 I. E. Taking the brakes off their immune system with or without GP100 make a difference. So kind of going through these like I'm, you know, it's my hobby and, and I don't read them that much. This, you can see it sort of skews about 60% to 40% male to FEMA. They talk about something called the ECOG performance status that refers to how healthy a patient is coming in. So ecog0 is not anymore. So it was kind of amazing how long it took me to remind myself of stuff I used to remember. But you do have to kind of go back and read the methods and figure out who were the patients in this, what was the eligibility criteria limitations whatsoever, which is kind of amazing when you really consider something. I think this speaks to just how devastating, devastating this disease is. These are patients who all have like six months to live, right? You know, a year max. And yet, look at this. 58 to 60% of them have no limitation on their quality of life at this very moment. That's going to change. Driperia, why did they do it this way? And of course, it all kind of radically, you know, absent a cure here. And then ecog1 has some limitation. I came back to me, but it took a minute. So. So the first thing is these are all patients who had progressed through every standard therapy. So these are patients for whom there were no other options. These patients either had very advanced stage three melanoma, which means it was local regional melanoma, but it couldn't be resected. So an example of that, that would be a cancer that was, you know, completely engulfing, like where, let's say the primary site was the cheek and it had completely grown into all of the surrounding soft tissue. It hadn't. And you can see that ecog1 plus ecog0 is basically 98% of the population. You can see the staging there. So, again, very, very few of these patients are the M0 category. M0 throws are people who have stage three disease that is so aggressive it can't be resected. That's about 1%. But the majority of these people are the M1A's, M1B's, M1C's. So these are people with very aggressive cancers. You can also see that about 10 to 15 bread anywhere. But it was, you know, all the lymph nodes of the neck. And I've seen patients like this and it's, you know, it's just completely disfiguring and they'd already been 15% of these people. People also have CNS metastases. Again, the poorest prognosis of the poor. And then you can see the. About 40% of them have the LDH level above cutoff. All of this is to say we're talking about a group of patients who have, you know, a very. Through the standard chemotherapy and nothing was working and the thing was growing and then it was mostly made up of patients with stage four cancer. Now, melanoma has a very, very funny staging cyst. High likelihood of not surviving more than, you know, a year. It would be very, you know, unlikely that many of these patients would survive more than a year. So basically, more than 70% of these people have visceral metastases, a third have high LDH, and 10, more than 10% have brain METs. They've also all progressed through standard therapy. So in cancer, we typically talk about something called the TNM stages staging system. It is the standard way that cancers are staged. T refers to the tumor size, N refers to the lymph node status, and M refers to the presence or absence of metastases. And for most. So radiation chemo. Yeah. And the chemo for. For. For melanoma can answer is. It is a very simple system. It is, you know, T is typically a number one, two supposed to. To be, you know, kind of a toxic chemo that. That really just doesn't really do anything.

So is it commonplace to use a treatment that failed in clinical trials as a placebo in these sorts of studies?

Yeah, it's interesting. I, I think you're referring obviously to the GP 100 and sometimes up to 3 and 4. N is typically 0, 1 or 2 and M is 0 or 1. Either there's no mean mets or there are mets. So for example, and I think the thinking was, okay, it hasn't been effective in other treatments, for example, when combined with IL2 or as an adjuvant, but never before has it been tried with a checkpoint inhibitor, which is the technical term for this type of drug. I think there was also some belief that it would be easier to enroll patients. I don't Colorectal cancer. The T staging determines the depth in the Think they stated this, but that's often the case. It would be easier to enroll patients if they would know that even in the placebo arm, they're still getting an active agent colon wall that it went. N is did it go?

Got it. And I suppose there's always the possibility that the combination of the failed drug with a new drug would work and Then so you're increasing the probability for.

Novel discovery to mets. And I think in colon I'm a little rusty on this. I think colon has n 0, 1 or 2 depending on how many lymph nodes and then m 0 did it go to anything beyond that like to the liver, lung, etc. Or not for sure. And again if you go back to the randomization of 3 to 1 to 1, it's really only 1/5 or 20% of the participants that would get just the GP100. So another melanoma is a bit more complicated. It has has m0 meaning no Mets, but it also has m1a, m1b, m1c and m1d. And within each of those you're basically telling people when they come into this study there's an 80% chance you're going to get anti CTLA 4. That's a much better set of odds than you know your has a threshold for high and low lactate dehydrogenase or ldh. So it's both a staging based on imaging and biochemical and the reason for typical study where you're going to be 50% likely to get the agent of.

Interest right in people who are literally dying of cancer that they. They don't want to be in the.

Control group or that is LDH level is such a strong prognostic indicator of survival in addition. Right, that's right. So the primary outcome for this study actually changed changed in the study into M staging. Higher LDH levels tend to reflect more acidity which we now they have to get permission to do that. But the so the original primary endpoint was the best overall response rate. So I have to explain how response rates are measured. This is, this is a bit complicated. Remember all of these patients by definition have measured talked about why that's problematic. Tends to reflect faster growing tumors, higher turnover, higher metabolic activity. M1A. Let me see if I can remember this. M1As are cancers that have metabol visible cancer by visible either on the surface of their body, but more likely on an MRI or CT scan. So all of these patients hestasized to surrounding soft tissue or soft tissue had to be scanned head to toe within 12 weeks of enrollment. Again, there's another thing I should point out here which I know you understand but it's always worth reminding people when a study like this takes place it usually do anywhere in the body. So anywhere else on the skin and you might think well that's kind of crazy. Like how does that happen? And it's really bizarre you can have a patient who had a melanoma that showed up in one part of their body and then they have metastases on other parts of their. Takes place over many years. And so it's not the case that all 700 of these patients were enrolled on the same day. And for finished, you know, we finished observing them on the same day. No, no. This took place for a very skin M1B is very long period of time. This took place across tens of centers. I can't remember if this was just globally or across the world. It might have been across the world. And so every center really needs to adhere to a very strict. And I always get B and C confused. I think B is the lung. So M1 protocol. And you have a central organization that is running this. So you have a drug company, I think this is Bristol, Bristol Myers Squibb that makes the drug, they provide the drug. And then you have a CRO or Clinical Research Organization is to the lung. M1C is to any internal organ, so liver etc and M1D is to the CNS. And as those numbers increase, as those legend that that is basically managing the trial. And the trial is being being done at cancer centers all over the world or all over the country and you know, enrollment, I think there's increased. The prognosis gets lower and lower and lower. So one of the first things I always look at when I look at a paper like this is tell me about the patient population. Like what, what was the, you know, what was the breakdown of patients began in 2008 for this? No, no, I think it completed in 2008. It probably started in about 2004, 2005. And therefore you had to kind of have real clear protocols around this. So complete. And in Table 1. So that's again, in clinical papers like this, Table 1 is always, always, always baseline characteristics. Response is the easier of these to understand. A complete response is everything vanishes completely. That's very rare in cancer therapy. Oh, I should mention one other thing and Andrew, this was done as a 3 to 1 to 1 randomization. So again in the. So instead what we kind of look for is a partial response. A partial response. And there is really different ways to define this. There are different criteria, but this is the most common way you define a partial response. A partial response is at least a 50% reduction by diameter. Because remember, in. In this type of imaging you're looking at 2D versus 3D. So if a simplest form a study would have two groups, right? You would have. We're Going to just have a treatment group and a placebo group. But in this arm you had three groups with one of them being the placebo. The placebo got just GP100, which is just a cancer vaccine, by the way. This is like you're looking at a lung lesion and it's this big. It had, you know, if it's 2 centimeters long long, it has to go to at least 1 centimeter in diameter. So it's a 50% reduction at least of every single lesion with no new lesions appearing and no lesions growing. So it's very strict criteria. Right. Again, CR means everything vanishes. Cancer vaccine that never showed any efficacy. So it was a cancer vaccine that had been tested both with Interleukin 2 directly and as an adjuvant for patients who had metastatic melanoma risk or had. Sorry, not. PR means at least a 50% by diameter, which by the way is a much bigger diameter, much bigger reduction in terms of tumor volume when you consider the linear versus the third power relationship of length and volume of every single lesion with nothing new appearing regardless of how small and no lesion growth growing. So metastatic melanoma who had melanoma resected, who were tumor free and then given the vac, that's a pr. So you basically have no response progression. We talk about those together and then partial response and complete response. So initially the the authors of the scene as adjuvants to see did that have an effect on outcomes and it didn't. So it's kind of a known placebo. So you had that group, then you had the anti CTL study. We're going to. The primary endpoint of this was going to be the best overall response rate. So what was the proportion of patients that hit pr? What was the proportion that hit a cr? That's very common in this type of paper where the outcomes are typically so dire. LA4 group and then you had anti ctla 4 plus gp 100. What's the rationale for the 3 to 1 to 1? It's basically it increases statistical power, however. Oh, I think I said, I think I said that the study was. I don't remember when the study ended. Right. So you know, this total study was a little under 700 people. But the amendment was made to change the primary endpoint to overall survival at some point during the study. So and by the way, that tends to be the metric everybody cares most about. So the overall survival for metastatic melanoma is zero, with the exception of people who respond to interleukin 2, high dose interleukin 2. And that will boost the overall survival rate to somewhere between 8 and 10%, very, very low. These patients, many of whom had already taken and progressed through Interleukin 2. Let me refresh my memory on what percentage of those patients. About a quarter of these patients had already taken high dose interleukin 2. And by definition, the fact that they're in this study means they had already progressed through that, that treatment had failed. Just reiterate, just kind of the state these patients are in. So now let's look at Figure 1. So again, I'll describe it because I realize many people are just listening to us. All of this will be available both in the video and then we'll link to the paper. So figure one is a figure that probably looks really familiar to people who look at, you know, any data that deal with survival. It's called the Kaplan mine entire survival curve. So on the x axis for this curve is time, and time here is shown in months. And on the Y axis is the overall survival at the very top, 100%, at the bottom, 0%. And it has three graphs or three curves that are superimposed on one another. For each, they put 400 in the anti CTLA 4 +GP 100 group and then you know, a little over 130 in each of the other two groups. So you're always going to be able to make these two comparisons, right? What you can check by doing this is is there any effective GP100 in this setting, which had never been done before? So again, GP100 is a known protein expressed by melanoma. And all of these people were haplotyped to make sure that their immune system would recognize it. And the question was, would giving people anti CTLA 4, I. E taking the brakes off their immune system with or without GP100 make a difference? So kind of going through this, you can see it sort of skews about 60% to 40% male to female. They talk about something called the ECOG performance status that refers to how healthy a patient is coming in. So ecog0 is no limitations whatsoever, which is kind of amazing when you really consider something. I think this speaks to just how devastating this disease the three groups, again, the control group, which is the GP100, the anti CTLA4 is, these are patients who all have like six months to live, right? You know, a year max group by itself. And the ntctla 4/gp 100. And one of the characteristics of a Kaplan Meier curve is by definition they have to be decreasing in a monotonic fashion. Fashion, because it's. And yet look at this. 58 to 60% of them have cumulative overall survival. That just means it can't like come down and go back up. No limitation on their quality of life. At this very moment. That's going to change. Nobody comes back to life. So once a person dies, they are censored from the study. And the curve drops and drops and drops and you can see that they kind of highlight. And I actually think it makes the graph a lot little harder to read when they, when they put some of those marks on there. But what really becomes clear when you look at this is that there's a key, there's a clear distinction radically, you know, absent a cure here. And then ecog1 has some limitation and you can see that ecog1 plus ecog0 is basically 98% of the population. You can see the. Between the curve for the placebo group, the GP100 group group, and the other two, the two treatment groups. Now you'll note at the very end that the two treatment groups appear to separate. A little staging there. So again, very, very few of these patients are the M0, but I'll talk about that in a second. So when I look category M zeros are people who have stage three disease that is so aggressive it can't be risky. Get these, Andrew. I. The first thing I always turn my attention to, I can't really resist. I have to look at the right hand side of the graph because what is that really telling me, right? The tail of this is showing me the true overall survival and I want to sort of figure out what is going on. So in the GP100 group, which is the placebo group, it is kind of amazing to think that there is still. That's about 1%. But the majority of these people are the M1A's, M1BS, M1CS. So these are people with very aggressive cancers. You can also see that about 10 to 15% of these people also have CNS metastases. Again, the poor one person who is alive at 44 months. It's amazing. I mean, it's both sobering and amazing that like one person made it to 44 months. The next thing I ask myself is, well, how long did half of the people make it? That's called median survival. And to do that you go up to the Y axis first prognosis of the poor. And then you can see the. About 40% of them have the LDH level above cutoff, all of this. And you draw a little line from the 50 over, and then you bring that down and. And that's, you know, that's. That's. That's awfully low. That's about. Yeah. In fact, the table will tell us exactly what that is because I think it's really hard to eyeball that stuff. Stuff. So let's go to. So there's always a table that will accompany these things. And let's pull up that table. I've got this paper spread out over so many things. Let's. Adverse events. Where's our survival table here? This is to say we're talking about a group of patients who have, you.

Know, a very subgroup analysis of overall survival.

It would probably be helpful if I stapled these things together because it would be.

Well, this is always a trade off, actually, for. Since this is a journal club episode. I. I will say that stapling helps, but it also prevents one from separating things out. Writing in the margin. So I like these little mini clips.

Yeah.

No financial relationship to the mini clips either. Just have to state that because I always get. If you don't say that, people go, oh, you must have a stake in these mini clips. I like these little mini clips. In fact, I'm such a nerd, I always have one of these pilot V5 V7s in my pocket, on my pocket or my hip. And then my pockets are always filled with. With these little mini clips. And. But then again, I have a friend who's a musician. He's. And he's always raining guitar picks. So, you know, it's an. As far as occupational hazards go of.

Being a nerd, I'm a big fan of the mini clip. High likelihood of not surviving. Surviving more than, you know, a year. But I went without it today. All right, so thank you. Yes. Table two. All right, so let's look at table two while looking at the Kaplan Meier curve, because now this allows us to see a couple of things. By the way, remember how I said there's like that one person who kind of is still alive in the treatment group? Well, you can tell that he's not a complete responder. He or she is not a complete responder. Because under evaluation of therapy in Table 2, it says best overall response, and it says complete responders, zero. So there was zero complete responders in the placebo. There were two partial responders. Again, a partial responder is. Some lesions got smaller, some got bigger. Stable disease is. It didn't really change that much.

Much.

And progressive Disease is obviously a year. It would be very, you know, unlikely that. That many of these patients would survive more than a year. So. So basically, more than 70% of these people have visceral metastases, a third have high LDH, and 10, more than 10% have brain METs. They've also all progressed through standard therapy. So radiation chemo. Yeah. And the chemo for. For. For melanoma can be, you know, kind of a toxic chemo that. That really just doesn't really do anything. It went beyond. Not.

When you say a partial response, like lesions got smaller. Are they literally just tracing the. The circumference of one of these, you know, skin lesions and saying, okay, it got bigger, smaller.

Yeah, literally, we'd had rulers in. Yep, Yep.

Gosh, this feels so crude in terms of like. Like, I mean, it makes total sense, but, like, in terms of, like, modern medicine. Oh, like your lesion grew from, like, 3 millimeters to 6 millimeters, and we're literally, like, drawing little boundaries around little blotches on the skin.

Yeah, you're. You're putting a little measuring tape on them. Now, again, most of these are happening in the radiology suite because most of the disease for these patients is inside the body. Remember, more than 70% of these patients had visceral metastases. So liver, soft tissue, lung, brain. You know, these are. In fact, if you include lung, liver, brain, and viscera, it's. It's all the. Pretty much all the patients. So most of this is looking at a CT scan or an MRI for the brain.

Got it.

Okay, so that's. That's kind of the first thing that comes up. The median response rate should. Should be shown pretty prominently here. So I'm looking through this, and where is median response? Maybe it's shown in a different table. Let's see. Not disease control rate, time to progression. I remember it's about 10 months, but maybe that's just in the text. Yeah, here it is. So I thought this would be in a table, but it's. It's on page 715 of the paper. It just reports it. So I'm sorry, I misspoke. The 10 months was for the anti ctla 4 plus gp 106.4 months for the gp 100 alone. That's the control. And then 10.1 for the anti ctla 4 alone.

Okay, so is it commonplace to use a treatment that failed in clinical trials as a placebo in these sorts of studies?

Yeah, it's interesting you're referring obviously to the GP100, and I think the thinking was, okay, it hasn't been effective in other treatments, for example, when combined with IL2 or as an adjuvant. But never before has it been tried with a checkpoint inhibitor, which is the technical term for this type of drug. I think there was also some belief that it would be easier to enroll patients. I don't think they stated this, but that's often the case. It would be easier to enroll patients if they would know that even in the placebo arm they're still getting an active agent.

Got it. And I suppose there's always the possibility that the combination of the failed drug with a new drug would work. And then so you're increasing the probability for novel discovery.

So again, I always. And again I'm just always doing this. I'm kind of going back to the paper to be like, does that make sense? And yeah, you kind of called it. Right. You said median survival was about eight. Well, it turns out it's actually like six and change because, because it has that little ding in it and it's out to a little past 10 on the two others. So the net takeaway here for sure. And again, if you go back to the randomization of 3 to 1 to 1, it's really only is again, just to put that in English because it's so profound, the 1/5 or 20% of the participants that would get just the GP100. So in other words, you're basically telling people when they come into this study there's an 80% chance 50% of the patients in the control group were dead and you're going to get anti CTLA 4. That's a much better set of odds than, you know, your six months. Months. 50% of the patients in the treatment group, both treatment groups were dead in 10 months. So what that means in cancer speak is these drugs extended median survival by four months. Now that's a, that's an important concept. You know, when we think about how has cancer therapy changed over the past 50 years? Median survival for metastatic cancer has increased across the board. So a person today with metastatic colorectal cancer or a woman today with typical study where you're going to be 50% likely to get the agent of interest. Right?

And people who are literally dying of cancer, they don't want to be in.

The control group, right? That's right. So the primary outcome for this study actually changed in the study study. Now they have to get permission to do that. But the, so the metastatic breast cancer or person with metastatic lung cancer, these people Will live longer with those diseases today, thanks mostly to treatments. This is not an early detection lead time bias issue. This is treatments are allowing people to live longer. And that's an important, important part of the story. But it's only half of the story. Yet it often gets touted as the story, the other half of the story, and frankly, the story that I think is more important is what is overall survival doing? And if you go back to those cancers, the answer is zero. So overall survival hasn't changed for solid epithelial tumors. It is. It was zero percent in 1970, and it's zero percent today.

Everyone dies.

Everyone dies from metastatic solid organ tumors. Now, again, there's those. There's those niche examples I gave you. Testicular cancer is now an exception. GI stromal tumors would be an exception. And I'm not including leukemias and lymphomas where now there are exceptions.

Okay, within. Not to try and be overly optimistic, but if I look at the graph in Figure 1, and I look out at the tail of the graph.

That's right.

And for those that are just listening, what I see. And I'm far less, Far less familiar with this type of work and analyzing these type of data, but what I see is that people in the placebo group, they're all dead, except that one. They're basically all dead at 44 months. But when I look at the number, how long it takes for everyone to be dead in the true treatment groups, it's like 50. Looks like 53, 54 months or something.

Well, and they're. And they're not dead. That's the point.

They're hanging in there.

Original primary endpoint was the best overall response rate. So I have to explain how response rates are measured. This is. This is a bit complicated. Remember, all of these patients, by definition, have measurable visible cancer by visible, either on the surface of their body, but more likely on an MRI or c CT scan. So all of these patients had to be scanned head to toe within 12 weeks of enrollment. Again, there's another thing I should point out here, which I know you understand, but it's always worth reminding people when a study like this takes place, it usually takes place over many years. And so it's not the case that all 700 of these patients were enrolled on the same day and finished, you know, we finished observing them on the same day. No, no, this took place for a very.

So, because. Because an extra. Somebody who lost both of my scientific advisors, two of the three, the other one to suicide. We've talked about this before, but the other two different cancers both had the BRCA2 mutation. By the way, an extra eight to 10 months with your kids or with your spouse or to quote, unquote, get your affairs in order is a big deal. I mean, it's still depressing in the sense that nobody survives lives long term, but, you know, an extra 10 months, as long as one is not miserable in that time, completely miserable. I mean, that's extra 10 months of living.

Right? Well, and what's interesting here is, you know, the observation period stops and some of these patients are still going. So what you're highlighting is kind of the point I want to make, which is overall survival is the most important metric and it's the highest bar. Make no mistake about it. And it's certainly not the bar any drug company is ever going to want to talk about for a cancer drug.

But why not? Because.

Because they don't. None of them work right. Like, we don't have, you know, like drugs.

They only want to talk about cures. They don't want to talk about.

No, they only want to talk about median survival. They want to. They only want to talk about extending median survival. And, you know, there are, you know, lots of people out there that are on this, on this platform. I don't need to get onto it, but who will say, like, look, it's a real racket in oncology today where drugs that are extending median survival by four weeks are being put on the market at a tune of 50 to $100,000 per treatment. That's not uncommon in oncology. There was one drug that was approved for pancreatic cancer. I believe it extended median survival by nine days and it cost $40,000.

And it's being advertised as significant.

Yes, extension. Because it was. That was a statistical significant improvement in median survival.

I'm just. Yeah. So it's.

Look, it's really understandable why people are very skeptical of the pharma industry. And, and I think, you know, a much more nuanced view is necessary. Clearly, I don't think pharma is all bad, but I really understand why people lose faith in pharma when, when, you know, these types of products somehow make regulatory approval.

Does insurance cover these kinds of drugs? Drugs?

It can. In fact, it often does. It depends on the FDA approval, of course, in the indicator long period of time. This took place across tens of centers. I can't remember if this was just globally or across the world. It might have been across the world. And so every center really needs to adhere to a very strict protocol. And you have a central organization that is running this. So you have a drug company, I think this is Bristol. Bristol Myers Squibb, that makes the drug, they provide the drug, drug. And then you have a CRO or clinical research organization that. That is basically managing the trial. And the trial is being done at cancer centers all over the world or all over the country. And, you know, enrollment, I think began in 2008 for this. No, no, I think it completed in 2008. It probably started in about 2004, 2005. And therefore you had to kind of have real clear protocols around this. So a complete response. Response is the easier of these to understand. A complete response is everything vanishes completely. That's very rare in cancer therapy. So instead what we kind of look for is a partial response. A partial response. And there is really diction. But a lot of times they do. Right. So yeah, there's a societal. Different ways to define this. There are different criteria, but this is the most common way you define a partial response. Cost to these things. But. But there's also a patient cost. Right. So a lot of times insurance, a partial response is at least a 50% reduction, doesn't fully cover it, and a patient has to bear the cost difference. And on top of that, you alluded to this a second ago, which is, what if your quality of life is dramatically compromised as a result of this treatment? And yes, statistically, you're going to live nine days longer or three weeks longer, but at what cost to your health in those final remaining days? And by the way, you're potentially straddling your loved ones with enormous debt in your absence. So it's. It's a super complicated topic.

Yeah, there's a dignity component too. I mean, I've seen this in people dying. You know, at some point they become.

Such a by diameter. Because remember, in this imaging, you're looking at 2D versus 3D BE.

So if a diminished version of their former selves that they don't want to be seen by people that way.

So what is exciting about this drug, although it's. This paper is not the. You're looking at a lung lesion and it's this big. It had, you know, if it's 2 centimeters long, it has to go to at least 1 centimeter in diameter. So it's a 50% reduction at least of every single lesion with no new lesions appearing and no lesions growing, growing. So it's very one that shows it. The reason I chose this paper, Andrew, is because it was the first approval. A second drug came along that is an anti PD1 drug. That drug is called very strict criteria. Right again, CR means everything vanishes. Keytruda. That drug turned out to be even better and had has even a greater response rate both in terms of median survival and overall survival. But this was the landmark paper. I also have a slight bias here and I'll disclose in a moment why, but I, but I think it just talks about very interesting biology. So let's talk about a couple things that stuck out to me in this paper. The first thing that stuck out to me and the authors didn't comment on it unless they did and I missed it, is look at Figure 2. So Figure 2 is the subgroup analyses where you're sort of showing a similar graph to the one you showed earlier, right? Where you, you show the response rate or the change in response between the groups and then you put the error bars on it. And this is where we talk about how. Well, it's a 95 confidence interval. So does it touch the unity line? So these are called like tornado plots. Typically. Typically. And what you'll notice is that in the top you're looking at sort of it's comparing the NTCTLA 4 with GP100 versus the GP100 and in the bottom you're looking at the NTCTLA 4 versus the GP100. So at a glance you can see GP100 is not doing anything. I mean that's the, that's the first takeaway of comparing a ton be. What I find most interesting is look at the subgroup analysis of females. Notice that in females, while there's a Trend towards risk, PR means at least a 50% by diameter, which by the way is a much bigger diameter, much bigger reduction in terms of tumor volume. When you consider the linear versus the third power relationship of length and volume of every single lesion with nothing new appearing, regardless of how small and no lesion growing. So that's a pr. So you basically have no response progression. We talk about those together and then partial response and complete response. So initially the, the authors of this study were going to. The primary endpoint of this was going to be the best overall response rate. So what was the proportion of pace reduction? And this is risk reduction for overall mortality. So again, I just want to restate that the primary outcome of this trial was changed to overall survival, which I think is the better outcome by the way. And overall for all patients in. When you compare anti CTLA 4 plus patients that hit PR, what was the proportion that hit a CR. Placebo versus placebo. There was a 31% risk reduction in overall mortality. That's what, that's, that's the mathematical interpretation of what you're seeing at the tail end of that Kaplan Meier curve. Living longer, living longer.

And it's a, it sounds like a big difference and in some sense it is a big difference.

Well, it is for those people because you're really looking at basically 0% surviving in the placebo group versus 20% of people are still alive at 56 months. And that's very common in this type of paper where the outcomes are typically so dire. However. Oh, I think I said, I think I said that the study would the treatment group. But look, that means 80% have died. Right? But notice that and, and, and sorry, when you just look at the anti CTLA 4 +GP 100 in the subgroup B, that hazard ratio's even showing more compression. It's a 36% reduction, reduction in risk of death. But notice that the females did not reach significance. So in the, in the first group they barely do. And you can see that because the confidence interval runs from 0.55 to 0.92. And notice the error bar almost touches the line. And in the second one it does not reach significance at all. So I actually went and kind of did a little reading on this after and I said, hey, you know, how much did this, this study, was this an outlier study? And it turned out it wasn't, was I? I don't remember when the study ended, but the amendment was made to change the primary endpoint to overall survival at, at some point during the study. So and by the way, that tends to be the metric everybody cares most about. So the overall survival for metastatic melanoma is zero. And that about half the studies of anti CTLA4 did indeed find that the drug was less effective in women than men, with the exception of people who respond to Interleukin 2. High dose Interleukin 2. Kind of interesting. Now, I couldn't find any great explanation for it, but the most plausible explanations fit into two categories. The first are maybe there are. And that will boost the overall survival rate to somewhere between 8 and 10% differences in the immune response to the drug if you're a man or a woman. The second comes down to dosing. I should have said this at the outset, but of course these drugs are not like a pill where it's like everybody gets, you know, 50 milligrams of this. They're all dosed based on weight. So this study is dosed I believe at 3 milligrams per kilogram. And because most men are heavier than women, men are getting a higher dose than women. And weight and body surface area and immune system like these things are not all perfectly linear. So I, I, I kind of wonder if this difference is simply explained by men on average getting a higher dose than women.

Interesting.

Last thing I want to talk about here is in Table 3. So Table 3, always an important table to look at in any paper is what are the adverse out? Very, very low. These patients, many of whom had already taken and progressed through Interleukin 2. Let me refresh my memory on what percentage of those patients. About a quarter of these patients had already taken high dose interleukin 2 comes. Right. What are the adverse effects of the drug?

Yeah, I spent a little bit of time with this and I confess it, I definitely don't want cancer to the extent that I can avoid it. But this table made me wonder whether or not I would also want to just avoid cancer treatment given the life extension provided. I mean these adverse events are pretty uncomfortable.

And by definition the fact that they're in this study means they had already progressed through that, that treatment had failed. Just reiterate, just kind of, just to put, just to put in perspective. And you always have to kind of, you know, be mindful of how many of these adverse events are occurring in people just because their disease is progressing. So the first thing I always want to look at is total adverse events in all three groups, not just great. So grade three and grade four are real toxicities. Right? Grade four toxicity is life threatening toxicity. By the way, grade three is pretty significant toxicity. Grade one and two, we typically just, you know, that's not that severe, right? Little rash, they put some corticosteroids on it, it went away kind of thing. Okay, so in the treatment plus GP100 group, 98.4% of people reported some event, so all but 1.6%. In the NTCTLA4 group alone it was 96.7%. So only 3.1% did not. But in the placebo group it's 97%. So it's important to keep in mind like, you know, everybody's having some adverse effect. Okay, well what if you say, well let's just limit it to the state these patients are in. So now let's look at figure one. So again I'll describe it because I realize many people are just listening to it. Us. All of this will be available both in the video and then we'll link to the paper. So figure most severe events. Well, let's just talk about grade four toxicities. There were 6.1% of those in the placebo group, 8.4%. And one is a figure that probably looks really familiar to people who look at, you know, any data that deal with survival. It's called the Kaplan Meier survival curve. So on the x axis for this curve is, IS time anti CTLA 4 group and 6.8% in the combined group. So not a huge difference in grade 4 toxicity.

Meaning that whatever adverse events are occurring may not be related to, they may.

Not be related to the treatment. Again, these are, if you, if you think about it, and it's a very awful, sad, morbid thought to imagine, these are, you're looking at the adverse responses of people, more than 80% of whom died during the course of a very, very short period study. And so, you know, it's very difficult to disentangle what effects or what side effects a person is having just from that process as they are from the actual treatment. But if there is an area where there's a really clear difference, it's down in the autoimmune category. So if you look at any immune related events, you can see that in the anti CTLA 4 plus GP100 group group, it's about 60% in both of those treatment groups versus 30%. And if you look at the grade 3 and 4 toxicities, it's 10% in the anti CTLA 4, 15% in the anti CTLA 4 alone group. And time here is shown in months and on the Y axis is the overgroup and only 3% in the treatment. So that's a real difference. Difference.

It makes sense that people getting this drug plus placebo or just the drug would have autoimmune issues because this is.

An immunotherapy, it's an immunomodulator. In fact, what is it doing? It is taking the brakes off the immune system.

But then again, the things that they list out, pruritus, is that a irritation of the skin?

Yeah, irritation of the skin.

I'm not a physician, but I know that any itis is going to be like an inflammation and oma, unfortunately, likely a cancer or cell replication.

Look at the difference in vitiligo, I mean raw survival at the very top, 100%, at the bottom, 0%. And it has three graphs or three curves that are superimposed on one another for each of the three groups. Again, the control group, which is the GP100. The anti CTLA4 group by itself and the anti CTLA4 plus GP100 and one of the characteristics of a Kaplan Meier curve is, by definition, they have to be decreasing in a monotonic fashion because it's cumulative overall survival. That just means it can't, like, come down and go back up. Nobody comes back to life. So once a person dies, they are censored from the study.

Wow. Yeah. So very.

Sorry. Sorry. Look at the gastrointestinal differences. Yeah. And the vitiligo. Right. So 3.7, 2.3%, 0.8%. The GI stuff is the most common. And the curve drops and drops and drops. And you can see that they kind of highlight them and stuff you're gonna see there. Those are. Those are the really big ones.

Now, of course, there's diarrhea and there's diarrhea.

Oh, yeah.

Like. Like there's travelers diarrhea. There's.

Yeah.

No, these overly.

Yeah. And these people.

I mean, for diarrhea. And then there's, like. Can't really feel. Do anything besides make trips back and forth to the bathroom.

Well, there's, there's. There's. Put it this way, there's, you know, colitis here. Is diarrhea so significant? These patients require IV fluids. Now, what. What you don't see here is how many of these patients actually required corticosteroids to reverse the autoimmunity. So a lot of times what'll happen here in these studies or with these drugs is the autoimmunity becomes so significant that you have to stop the drug and give corticosteroids, do the exact opposite. You now have to shut the immune system down. Down. So you just took the brakes off it with the drug, and now you need to shut it down with corticosteroids. When I was. Was I in med school? No. When I was in my fellowship, I wrote a paper about autoimmunity correlating with response rate in anti CTLA 4 early on, this was during the phase 2 work, so. So the NCI was a very early adopter of participating in these trials. And, you know, it was observed that, or at least hypothesized. This is what the paper basically wrote about, which was, is there any correlation between. And I actually think it makes the graph a little harder to read when they. When they put some of those marks on there. But what really becomes clear when you look at this is that there's a key. There's a clear distinction between the curve for the placebo group, the GP100 group and the other two, the two treatment groups. Now you'll note at the very end that the two treatment groups appear to separate a little bit. I'll talk about that in a second. So when I look autoimmunity and response and it turned out that these. Andrew, the first thing I always turn my attention to, I can't resist. I have to look at the right hand side of the graph because what is that really telling me, right? The tail of this is showing me the true overall survival. The answer was yes, there was a very strong correlation. So there was no difference in autoimmunity between the doses. And so the paper we wrote was two dosing schedules. So it was basically the full dose, the 3 milligrams per kilogram versus a low dose, 1 milligram per kilogram. This is a F2 trial. Those are your two arms. There turned out to be no difference in autoimmunity between them, but there was a big difference between. And I want to sort of figure out what is going on. So in the GP100, the response rate that tied to autoimmunity. In other words, autoimmunity, predicted response. Now, I think over time these investigators, the doctors who administer these treatments are getting better and better at catching these things earlier because these autoimmune conditions can actually be devastating. So on a very personal note, when Keytruda came out, I want to say it was around 2011. No, no, no. Gosh, it must have been 2013, 2014, thereabouts. Again, it was for treatment of metastatic melanoma. I want to come back and explain why melanoma gets all of the attention in autoimmune condition in, in immunotherapy group, which is the placebo group. It is kind of amazing to think that there is still one person who is alive at 44 months. It's amazing. I mean it's both sobering and amazing that like one person made it to 44 months. The next thing I ask myself is, well, how long did half of the people make it? That's called median survival. And to do that you go up to the Y axis and you draw a little line from the 50 over and then you bring that down. Conditions. I'll state that. But, but anyway, a friend of mine got pancreatic cancer and he got the bad type of pancreatic cancer. So this is an, like the adenocarcinoma of the pancreas, right? So these, this is a, a non survivable type of cancer. Furthermore, his was unresected so can you.

Explain what that is?

Yeah. So the only. So about 20% of people who have pancreatic cancer technically have it in a way where you could still take out the head of the pancreas.

Right. The Whipple procedure.

The Whipple procedure. Now tragically, most of those patients will still recur.

My understanding is that pancreatic cancer progresses from anterior to posterior in the pancreas.

And that's, you know, that's awfully low. Oh, that's about. Yeah. In fact the table will tell us exactly what that is because I think it's really hard to eyeball that stuff. So let's go to. So there's always a table that will accompany these things. And let's pull up that table. I've got this paper spread out over so many things. Let's. Adverse events. Where's our survival here?

Figure 2. Subgroup analysis of overall survival.

It would probably be helpful if I stapled these things together because it would be Chris.

And that the Whipple is a removal of the front end, the anterior. That's the Whipple procedure. So if the cancer has progressed far enough caudal into the posterior pancreas, then there's nothing left to cut out. Basically. Well, can we survive without a pancreas for any amount of time?

Oh yeah, absolutely.

So why don't they just remove the whole pancreas?

Oh that's.

This is always a trade off actually for. Since this is a journal club episode, I will say that stapling help my point.

It's already micro metastasized. So it's not. The surgical procedure is not the challenge anymore.

But it also prevents one from separating things out writing in the margin. So I like these little mini clips. Yeah, no financial relationship to the mini clips either.

Just used to be so you know, at Johns Hopkins, which is one of the hospitals where this was pioneered like, like the 30 day mortality for a Whipple procedure was I don't know, 80%. And the reason was to figure out.

How to state that because I always get. If you don't say that people go oh you must have a stake in these mini clips.

To the bowel without the. So the pancreas systems.

I like these little mini clips. In fact I'm such a nerd. I always have one of the. These pil.

Such an awful organ to operate on because its enzymes are designed to digest.

V5 V7s in my POC on my pocket or my hip. And then my pockets are always filled with. With these little mini clips and. But then again I have a friend who's a musician. He's. And he's always raining anything and everything.

So imagine now you have to cut the pancreas in half, take out the head of the pancreas with the duodenum and then, then somehow so that tar picks.

So you know, it's an. As far as occupational hazards go of being a nerd.

No, I'm a big fan of the mini clip. Is that open half of a raw pancreas to the end of the jejunum and not let it digest itself.

Someone at Hopkins figured this out?

No, the first one was actually done by A.O. whipple. But yes, at Hopkins is where they figured out the way to put drains in the surgical technique. How to do it in two layers, what type of stitches to you. But I, I went without it today. All right, so thank you. Yes. Table two. All right, so. So let's look at table two while looking at the Kaplan used. Like all of the nuances of this were worked out in a few places, but I would say Hopkins more than any place else.

And are there physicians who like try this on non human primates or something or is this always just done on patients and it.

Well, nowadays, I mean, put it this way, even, even 25 years ago at a, at a, at a major center like Hopkins, the, the mortality of that procedure was less than meier curve. Because now this allows us to see a couple things. By the way, remember how I said there's like that one person who kind of is still alive in the treatment group? Well, you can tell that he 1%.

Amazing.

Yeah.

So there have been some victories.

Well, yes, but here's my point. It that that's no longer the bottle neck. Right. Taking out the pancreas safely, as complicated and challenging as that is. And if you need a whip up procedure, you only want to have it done by someone who just does that night and day because it's. You don't want weekend warriors doing it. That's not why people are living or dying. They're dying because the pan, the cancer just comes back. It was always not a complete responder. He or she is not a complete responder because under evaluation of therady spread to the liver, by the time you did it, you just didn't realize it it yet. So whether you took out the whole pancreas or the head of the pancreas, or the tail of the pancreas, the location of the tumor is predictive of survival. In table two it says best overall response and it says complete responders Zero. So there was zero complete responders in the placebo. There were two partial responders. Again, a partial responder is. Some lesions got smaller, some got big, bigger, stable. Only in the extent that it basically is a window into how soon did symptoms occur. So pancreatic cancers in the tail tend to be more fatal, even though able disease is. It didn't really change that much. And progressive disease is obviously, they're way easier surgically to take out, because by the time you develop symptoms of a tail pancreas cancer, it's a big cancer.

I was going to ask this question later, but I'll just ask it now. Given the link between the immune system and these cancers, is there an idea in mind that people who are, let's say, 40 and older or 50 and older, who don't yet they're not diagnosed with any cancer, would periodically just stimulate their immune system to wipe out whatever early cancers might be cropping up. You know, just take a drug to just ramp up the immune system, even to the point where you start having a little diarrhea, maybe a few skin rashes, and then come off the drug. You know, just basically to fight back whatever little cell growths are starting to take place in skin or liver or, you know, maybe for it.

It went beyond not.

When you say a partial response, like lesions got smarter. They literally just. Just tracing the. The circumference of one of these, you know, skin lesions and saying, okay, it got bigger, smaller.

Yeah, literally.

We'd had rulers in biology.

Yep. Yep.

This feels so crude in terms of like, Like, I mean, it makes total sense, but, like, in terms of, like, modern medicine. Oh. Like your lesion grew from, like, 3 millimeters to 6 millimeters, and we're literally, like, drawing little boundaries around little blotches on the skin.

Yeah. You're. You're putting a little measuring tape on them. Now, again, most of these are happening in the radiology suite for, you know.

Three weeks out of each year. I mean, why not?

Yeah, it's an interesting question. I've never thought of it through that lens. I suppose the question is, what can we do to keep our immune systems as healthy as possible as we age?

Because stay on a normal circadian schedule. There's evidence for that.

Sure. No, there's evidence that certain. Because most of the disease for these patients is inside the body. Remember, more than 70% of these patients had visceral metastasis. If it promotes sleep, anything that promotes better rest. So liver, soft tissue, lung, brain. You know, these are, in fact, if you include lung Liver, brain and viscera. It's, it's all pretty much all the patients. So most of this is looking at a CT scan or an MRI for the brain is going to promote immune health. Because if you ask the macro question which is like why does the prevalence of cancer increase so dramatically with age? There are certain diseases where it's really obvious why the prevalence of the disease increases with age.

Yeah, like Mac, like age related macular degeneration.

Sure. Or cardiovascular disease is by far the most obvious because it's an.

Got it.

Okay. So that's, that's kind of the first thing that comes up the median response rate area under the curve exposure problem. The more exposure to lipoprotein and the more the endothelium gets damaged, the more likely you are to accumulate plaque. And again it totally makes sense why 10 year olds don't have heart. Should, should be shown pretty prominently here. So I'm looking through this and where is median response? Maybe it's shown in a different table. Let's see. Attacks and 80 year olds do. But when you sort of acknowledge that well hey, you know, can't you know anybody's accumulating genetic mutations. We're always surrounded and being not disease control rate time to progression. I remember bombarded by things that are altering the genome of our cells. Is it simply a stochastic process where the longer you live, the more of these mutations you're going to occur until at some point one of them is just wins. I, I think that's got to be a big part of it, but I think another part of it, and I clearly I'm not alone in thinking this is that our immune system is getting weaker and weaker as we age. Right. I mean you know, we, you know, people become more susceptible to infections as they get older and I think that that's equally playing a role in our susceptibility to cancer. So yeah, I think the question is how do you modulate immunity as you age age. And to me that's one of the most interesting things about rapamycin potentially is that when taken the right way, it seems to enhance cellular immunity which again that, that's potentially a really big deal again at least in, in short where it's about 10 months. But maybe that's just in the text. Yeah, here it is. So I thought this would be in a table, but it's, it's on page 715 of the paper. It just reports it. So I'm sorry, I misspoke the term. Human experiments in response to vaccination it's enhancing vaccine response. So the question is, would that translate into cancer? Nobody knows. Could that be one of the reasons why animals treated with rapamycin live longer and get less cancer? Don't know. You know, it could also be that it's, it's at a fundamental level that's targeting nutrient sensing where 10 months, months was for the anti ctla 4 plus GP 106.4 months for the GP 100 alone. That's the control. And then 10.1 for the anti ctla 4 alone. Okay, going with that story was that maybe I'll back up for a moment. Why melanoma? So we didn't really know this like, like 30, 40 years ago in the early days of immunotherapy. But what we know now is that most cancers probably have about 40 mutations in them. So again, I always, and again I'm just always doing this. I'm kind of going back to the paper to be like, does that make sense? And yeah, you kind of called it right. You said median survival was about 8. Well, it turns out it's actually like 6 and change. That's like ballpark. 4050 mutations is standard fare for a cancer. But melanoma happens to be one of the cancers that has many, many more mutations. And the more mutations a cancer has, the more likelihood that it will produce an antigen that's recognized as non self. And that's why in the early days of immunotherapy, the only things that worked were IL2 against metastatic melanoma and kidney cancer. Because kidney cancer turned out to also be one of those cancers that for reasons that are not clear, produced hundreds of mutations. And so it's no surprise that the early studies of checkpoint inhibitors were also done in metastatic melanoma because it has that little ding in it. And it's out to a little past 10 on the two others. So the net takeaway here is again just to put that in English because It's so profound, 50% of the patients in the control group group were dead. Where you basically have more shots on goal. Again, if I'm going to take the brakes off my immune six months, 50% of the patients in the treatment group, both treatment groups were dead in 10 months. So what that means in cancer speed system, I might as well do it in an environment where there are more chances for my T cells to find something to go nuts against. So it's 2013, 2014 and this friend of mine who has something called lynch syndrome, which is a one of those Few hereditary or germline mutations that results in a huge increase in the risk of cancer. He had all is these drugs extended median survival by four months. Now that's our, that's an important concept. You know, when we think about how has cancer therapy changed over the past 50 years. Median survival for metastatic cancer has increased across the board. So a person today already had colon cancer at about the age of 40 and had survived that. It was a stage three cancer but he had survived it well. Now five years later had developed pancreatic cancer cancer. And when he went to see the surgeon, they said yeah, we, there's nothing we can do. Like it's too advanced. So that's, you know, to put that in perspective, that is a death sentence. And that's not that, that's a, that's a six month survival. And with metastatic colorectal cancer or woman today with around that time there was a study that had come out in the New England Journal of Medicine that had talked about how patients with lynch syndrome had lots of mutations and metastatic breast cancer or person with metastatic lung cancer. These people will live longer with those diseases today thanks mostly to treatments. This is not an early detection lead time bias issue. This is treat. So we you know, talked with his doctors about the possibility of enrolling him in one of the keytruda trials cells. There was one going on I think at Stanford. And you know, the thinking being, well, you know, you would want to target a checkpoint inhibitor against somebody who has a lot of mutations. And even though typically we don't see that in pancreatic cancer, his is a unique variant of it because it's based on this mints are allowing people to live longer. And that's an important part of the story. But it's only half of the story yet it often gets touted as the story story, the other half of the story. And frankly the story that I think is more important is what is overall survival doing. And if you go back to those cancers, the answer is zero. So overall survival. And so sure enough, he was tested for these mismatch repair genes. He had them enrolled in the trial and amazingly had not only a complete regression of his cancer and he's still alive in cancer free today 10 years later. But the treatment worked so well at activating his immune system that his immune system completely destroyed his pancreas. So now he has effectively had a pancreatectomy. Hasn't changed for solid epithelial tumors. It was 0% in 1970 and it's 0% today everyone dies. Everyone dies from metastatic solid organ tumors. Now again, there's those, there's those niche examples I gave you. Testicular cancer is now an exception. GI stroke based on his immune system. So now he actually has type 1 diabetes. He has no pancreas.

He injects insulin.

Yeah, no, he's. No, no, he has to use insulin. Just like someone with type 1 diabetes.

He had to pick being alive with type 1 diabetes.

Yeah, of course. And no comparison, but it's just an interesting example of how, how you know, remarkable this treatment was able to work when you were, you know, you could completely unleash the immune system of a person and you eradicate the cancer and the rest of the cells around it. And, and you know, there are many organs we could live without. You know, there are certain organs you can't live without. You can't live without your heart, lungs, liver, kidneys. But, but many things that kill people arise from organs. The breast, you could live without all breast tissue. Prostate, you can live without all prostate tissue.

Would choose to do. To live without these. But.

Right, but I'm saying if you normal tumors would be an exception. And I'm not including leukemias and lymphomas where now there are exceptions.

Okay. Within. Not to try and be overly optimistic, but if I look at the graph in Figure 1 and I look out at the tail of the graph.

That's right, right.

And for those that are just listening what I see and I'm far less, far less.

If you had metastatic cancer and you had a bullet that could selectively target a tissue, you would take it. And right now the only tissue we can do that against is a CD19B cell. And that's what those car T cells are. So right now these are not tissue specific treatments, but they're mutation specific. The last thing I'll say about this paper that I found interesting, interesting and I was looking for it and I was surprised they didn't at all comment.

On familiar with this type of work and this analyzing these type of data. But what I see is that people in the placebo group, they're all dead except that one.

If there was any correlation between autoimmunity and response. So they obviously acknowledge the autoimmunity in, in Table 3. But I would have loved to have seen a statistical analysis that said hey, hey. Is there any correlation between response rate and autoimmunity? Yep.

They're basically all dead at 44 months.

Yep.

But when I look at the number how long it takes for everyone to be dead in the true treatment groups.

But they didn't comment to that effect. So we're left kind of wondering what the current state of that is. And I guess in summary I'll say that the reason I thought this was an interesting paper to present is that I still believe that immunotherapy is probably 50.

Looks like 53, 54 months.

Well, and they're. And they're not dead. That's the point.

They're hanging in there.

The most important hope we have for treating cancer and well, so because you.

Know an extra somebody who lost both of my scientific advisor, two of the three, the other one to suicide. We've talked about this before, but the other two different cancers both had the BRCA2 mutation.

I think we're still only scratching the surface of it. So collectively the overall survival increase for patients with metastatic solid organ tumors is about 8% better than it was 50 years ago. And virtually all of that has come from some form of immunotherapy I think is promising thing by the way, you.

Know, an extra eight to 10 months with your kids or with your spouse or to quote unquote.

And I think the holy grail is that meaning the next step, if you go back to where we started, get.

Your affairs in order is a big deal. I mean it's still depressing in the sense that nobody survives long term.

The discussion is coming up with ways to eng.

But you know, an extra 10 months as long as one is not miserable in that time.

Engineer T cells to be even better recognizers of antigens. And there's many ways to do that. One is to directly engineer them. Another is to find T cells that have already migrated into tumors. Those are called tumor infiltrating lymphocytes or till and expanding those and engineering them to be better and younger. Younger.

Is it possible to engineer our own T cells to be more ph variant tolerant? Meaning since this, you know, cloaking of the. Of a local area by changing the ph. Can. Could we, you know, pull some T cells? I'm always thinking about the inoculation stuff like pull some T cells as part of our standard exam when we're 30 and you know, and grow some up in an environment that the phone is. Is slightly more acidic. I'm completely miserable. I mean that's extra 10 months of living right than than normal and then reintroduce them to the body.

Well and, and what's interesting here is, you know, the observation period stops and some of these patients are still going. So what you're highlighting is kind of the point I want to make, which is overall survival is the most important metric, and it's the highest bar. Make no mistake about it.

And after all, they are our T cells. In other words, give them a little opportunity to evolve the. The conditions they can thrive in. Right? Or even just keep them in the freezer in case we need them.

So the interesting thing is, I don't know that if you just got them to be comfortable in a lower ph, it would be sufficient, because there are still. It's certainly not the bar are any drug company is ever going to want to talk about for a cancer drug.

But why not? Because.

Because they don't. None of them work right. Like, we don't have, you know, like.

They only want to talk about cures. They don't want to.

No, they only want to talk about median survival. They want to. They only want to talk about extending median survival. And, you know, there are, you know, lots of people out there that are on this. So many other things that the cancer is doing as far as using other secreting factors. It seems that by far the most potent thing comes down to expanding the number of T cells that recognize the antigen and making sure that you can get that number big enough without aging them too much. So in some senses, it has become a longevity problem of t cells. The way to think about it is you want an army of soldiers who are wise on this platform. I don't need to get onto it. But who will say, like, look, it's a real racket in oncology today, where drugs that are extending median survival by four weeks Are being put on the market at a tune of, you know, 50 to $100,000 per treatment. That's not uncommon in oncology. There was one drug that was approved for pancreatic cancer. I believe it extended median survival by nine days. Enough to recognize the bad guys, which comes with age, but young enough to go and kill. And right now, both extremes seem to be unhelpful. Right. When you go and find tumor infiltrating lymphocytes in a tumor, they're very wise. They know which one. They've demonstrated that they can do everything. They can outmaneuver the cancer, but they're too old to do anything about it. And when you take them out to try to expand them by three laws, bugs, which is typically what you need to do, Expand them by a thousand fold, they can't do anything.

Got it.

And it costs $40,000.

And it's being advertised as significantly, yes.

Extension because it was. That was a statistical significant improvement in median survival. I'm just.

Yeah, so it's.

Look, it's really understandable why people are very skeptical of the pharma industry. And, and I think you know, a much more nuanced view is necessary. Clearly I don't think pharma is all bad, but I really understand why people lose fear faith in pharma when. When you know these types of.

And what about avoiding melanoma altogether? I mean obviously avoiding sunburn. You know, I somehow I got couched as anti sunscreen and that is absolutely not true. I, I said some sunscreens contain things that are clearly immune disrupt endocrine. Excuse me, disruptors. And we're going to do a whole episode on sunscreen. Maybe we could do some.

It's funny, I think I'm. I'm actually planning something on that as well.

Yeah, I mean and some dermatologists reached.

Out some very product somehow make regulatory approval.

Does insurance cover these kinds of drugs?

It can. In fact it often does. It depends on the FDA approval. Of course in the indicate very skilled.

Dermatologist reached out and said that. Indeed.

But a lot of times they do. Right. So yeah, there's a societal cost to these things but. But there's also a patient cost. Right. So a lot of times insurance, some.

Sunscreens are downright dangerous. But of course melanoma is super dangerous. Dangerous physical barrier. No one disputes physical barriers for sunscreen.

Right.

Everyone, everyone agrees that that is unlikely to have endocrine disruption. So physical barriers are undisputed. But aside from limiting sunlight exposure to the skin, what are some other risks for melanoma?

Doesn't fully cover it and a patient has to bear the cost difference. And on top of that, you alluded to this a second ago, which, which is what if your quality of life is dramatically compromised as a result of this treatment? And yes, statistically you're going to live nine days longer or three weeks longer, but at what cost to your health in those final remaining days? And by the way, you're potentially. I mean, I think that's the biggest one. I do not believe that smoking poses a risk for melanoma. And if it does, it's going to be very small. There are hereditary cases, so one needs to. To be pretty mindful when taking a family history. And by the way, there are really weird genetic conditions that link melanoma to other cancers such as pancreatic cancer, by the way. So whenever I'm taking somebody's family history and I hear about straddling your loved ones with enormous debt in your absence. So it's a super complicated topic.

Yeah, there's a dignity component too. I mean I've seen this in people dying. At some point they become such a.

Somebody that had melanoma and someone that had pancreatic cancer. I'm. There's a couple genetics, genetic tests we'll look at to, to see if that's a person that's particularly sensitive just. And a. From a genetic predisposition. But I do think that first and foremost it's, and by the way, I think with melanoma that although it's not completely agreed upon, I think it's less about sun exposure and more about sunburn. Right. So, so. And again, I'm sure there's some.

A diminished version of their former selves that they don't want to be seen by people that way.

Somebody listening to this who will chime in and apply a more nuanced response to that. But, but I think there's a, there's a fundamental difference between I'm out in the sun, getting sun, making some vitamin D versus I'm getting scorched and you know, undergoing significant UV damage image. There might also be something to be said for the time in one's life and I've certainly seen things that suggest that early, you know, early repeated sunburns would be more of a risk. So look, I think that's not a controversial point in the sense that like who wants to be sunburned? Right. So it's like whatever one needs to do to be sunburned, whether it's, you know, you know, being mindful of what the UV index is, wearing the appropriate cover, wearing the appropriate sunburn screen. So what is exciting about this drug? Although it's. This paper is not the one that shows it. The reason I chose this paper, Andrew, is because it was the first approval. A second drug came along that is an anti PD1 drug. That drug is called Keytruda. That drug turned out to be even better and had. Has even. I mean, I also find the whole kind of anti sunscreen establishment to be a little bit odd.

Well, the anti sunscreen establishment is odd. You know, I'm trying to open the door for a nuanced discussion about, you know, the fact that some sunscreens really do contain things like oxybenzenes and things that are real. Yeah, but when you kids, you're spraying them on kids.

Yeah, but you just look at the straight of, you know, the good old fashioned mineral sunscreen.

Perfectly safe.

Yeah.

Yeah, as far as we know.

I mean, great response rate both in terms of median survival and overall survival. But this was the landmark paper. I also have a slight bias here and I'll disclose in a moment why. But. But I think it just talks about very interesting biology. So let's talk about a couple of things that stuck out to me in this paper. The first thing that stuck out to me and the author.

I also dare we cross the seed oil debate into this. Some of the folks who are really anti seed oil also claim that seed oils increase risk for sunscreen. Peter and I are smiling because we have teed up a debate soon with some, you know, anti seed oil and less anti seed oil experts. So that that's forthcoming. That's going to be a fun one. We'll be doing all of that with our shirts on. I really appreciate you walking us through this paper, Peter. I have never looked at a paper.

On cancer or didn't comment on it unless they did and I missed it is look at Figure 2. So Figure 2 is the subgroup analyses where you're sort of showing a similar graph to the one you showed earlier. Right. Where you. You show the response rate or the change in risk.

And certainly not one like this. I learned a lot and, and it's such an interesting field, obviously because of the importance of getting people with cancer to survive longer and lead better lives, but also because of the interaction with the immune system. So we learned some really important immunology.

Yeah. And this was great. I feel much more confident now in the bonds between the groups. And then you put the error bars on it. And this is where we talk about how. How. Well, it's a 95% confidence interval. So does it touch the unity line? So these are called like tornado plots typically. And what you'll notice is that in the belief that the, the exposure to light early and late in the day can actually have. Have benefit top, you're looking at sort of it's kids tonight. And as I said, I think that there's. I think there's some causality here and I think it shouldn't be ignored. Cool.

Well, this was our second journal club. I look forward to our third. Next time you'll go first. We'll just keep alternating. We've also switched venues, but we both wore the correct shirt. And I hope people are learning and not just learning the information, but learning how to parse and think.

Comparing the NTCTLA 4 with GP100 versus the GP100. And in the bottom, you're looking at the NTCTLA 4 versus the GP100. So at a glance you can see GP100 is not doing anything. I mean that's the, that's the first takeaway of comparing A to B. What I find most interesting is look at the subgroup analysis of females. Notice that in females while there's a trend towards risk about papers and I.

Certainly learned from you. Peter, thank you so much.

Yeah, thanks Anderson.

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Both Spotify and Apple reduction and this is risk reduction for overall mortality. So again I just want to restate that the primary outcome of this trial was changed to overall survival, which I think is the better outcome by the the way. And overall for all paid.

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In when you compare anti ctla 4 + Sode.

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Placebo versus placebo there was a 31% risk reduction in overall mortality. That's what, that's, that's the mathematical interpretation of what you're seeing at the tail end of that Kaplan Meer curve. Living longer, living longer.

And it's a, it sounds like a big difference and in some sense it is. People derive tremendous benefit from from them for things like improving sleep, for hormones.

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Yet basically 0% surviving in the placebo group versus 20% of people are still alive at 56 months in the treatment group. But look, that means 80% have died, right? But notice that and sorry when you just look at the anti ctla 4.

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Exposure, exercise protocol plus GP100 in the subgroup B that hazard ratios even showing more compression it's a 36% reduction in.

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But notice that the females did not reach significance. So in the first group they barely do. And you can see that because the confidence interval runs from 0.55 to 0.92 and notice the error bar almost touches the line and in the second one it does not reach significance inter all. So I actually went and kind of did a little reading on this after and I said hey, you know how much did this study? Was this an outlier study? And it turned out it wasn't and that about half the studies of anti CTLA 4 did indeed find that the drug was less effective in women than men, which I found interesting. Now, I couldn't find any great explanation for it, but the most most plausible explanations fit into two categories. The first are maybe there are differences in the immune response to the drug if you're a man or a woman. The second comes down to dosing. I should have said this at the outset, but of course these drugs are not like a pill where it's like everybody gets you know, 50 milligrams of this. They're all dosed based on weight. So this study is dosed I believe at 3mg per kg and because most men men are heavier than women, men are getting a higher dose than women and weight and body surface area and immune system. Like these things are not all perfectly linear. So I, I, I kind of wonder if this difference is simply explained by men on average getting a higher dose than women.

Interesting.

Last thing I want to talk about here is in Table 3. So Table 3, always an important table to look at in any paper is what are the adverse outcomes? Right. What are the adverse effects of the drug?

Yeah, I spent a little bit of time with this and I confess it, I definitely don't want cancer to the extent that I can avoid it. But this table made me wonder whether or not I would also want to just avoid cancer treatment given, given the life extension provided. I mean, these adverse events are pretty uncomfortable.

They sound like just to put, just to put in perspective. And you always have to kind of, you know, be mindful of how many of these adverse events are occurring in people just because their disease is progressing. So the first thing I always want to look at is total adverse events in all three groups, not just grade. So grade three and grade four are real toxic, right? Grade four toxicity is life threatening toxicity. By the way, grade three is pretty significant toxicity. Grade one and two, we typically just, you know, that's not that severe, right? A little rash to put some corticosteroids on it, it went away kind of thing. Okay, so in the treatment +GP100 group, 98.4% of people reported some event, so all but 1.6% in the NTCTLA4 group.