The Cancer Doctor Podcast

#1 - Jonathan Stegall MD: From Preemie to Integrative Oncologist

Episode Summary

In the very first episode of The Cancer Doctor Podcast, we sit down with leading integrative oncologist Jonathan Stegall M.D., an integrative oncologist from Atlanta. Dr. Stegall shares his personal background, which includes being born premature and overcoming health challenges in his own life. He recalls being inspired by his grandmother's courageous fight with stomach cancer, which ultimately led him to pursue a career in medicine. This exclusive podcast interview covers topics such as the importance of a patient-centered approach to healthcare, the benefits of combining conventional and alternative treatments, and the need for greater empathy and humanity in medicine. This episode is sponsored by the Center for Advanced Medicine, located just outside of Atlanta, Georgia.

Episode Notes

Looking to get in touch with Dr. Jonathan Stegall MD? CLICK HERE

#1 - Jonathan Stegall M.D. | From Preemie to Integrative Oncologist

ℹ️ About This Episode

In the very first episode of The Cancer Doctor Podcast, we sit down with leading integrative oncologist Jonathan Stegall M.D., an integrative oncologist from Atlanta. Dr. Stegall shares his personal background, which includes being born premature and overcoming health challenges in his own life. He recalls being inspired by his grandmother's courageous fight with stomach cancer, which ultimately led him to pursue a career in medicine. This exclusive podcast interview covers topics such as the importance of a patient-centered approach to healthcare, the benefits of combining conventional and alternative treatments, and the need for greater empathy and humanity in medicine. This episode is sponsored by the Center for Advanced Medicine, located just outside of Atlanta, Georgia.

⏰ Timestamps

[00:01:00] Premature birth and destiny.
[00:04:31] Alternative medicine and science.
[00:09:23] Patient-centric approach in medicine.
[00:10:21] Doctor's Lack of Time for Learning.
[00:13:39] Insurance and healthcare system.
[00:17:14] The future of cancer treatment.
[00:21:50] History of chemotherapy.
[00:23:39] Fractionated metronomic chemotherapy.
[00:28:20] Accumulation of chemotherapy doses.
[00:30:07] Chemotherapy for cancer treatment.
[00:33:29] Insulin potentiation therapies.
[00:39:07] Integrative Oncology and Hyperthermia.
[00:40:12] Local hyperthermia and cancer treatment.
[00:43:42] Insulin and Cancer Treatment.
[00:47:21] Cancer imaging and testing.
[00:53:42] Cancer recurrence and monitoring.
[00:56:08] Fractionated chemotherapy and financial incentives.
[00:58:01] Low dose chemo vs full dose.
[01:01:23] Cancer diagnosis and treatment.

📚 Additional Resources Mentioned in this Episode

  1. The Center for Advanced Medicine on Cancer Doctor
  2. Dr. Jonathan Stegall on Cancer Doctor
  3. Dr. Jonathan Stegall on Facebook
  4. Dr. Jonathan Stegall on Instagram
  5. Dr. Jonathan Stegall on Twitter
  6. Cancer Secrets Book
  7. Cancer Secrets Podcast
  8. Cancer Secrets University
  9. Cancer Secrets Website
  10. The Center for Advanced Medicine Website

🥼 About Cancer Doctor

We exist to match cancer patients with the best integrative doctors in the world. If you or a loved one are looking for additional options for cancer care, please visit cancerdoctor.com and have a look through our Partners and Certified Doctors.

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📺 Episode Info

Podcast Name: The Cancer Doctor Podcast
Episode & Title Number: Season 1 Episode 1
Date: Recorded on March 15th, 2023
Episode Transcript Link

Disclaimer

The information presented in this podcast is for educational and informational purposes only. The content is not intended to be a substitute for professional medical advice, diagnosis, or treatment. Always seek the advice of your physician or other qualified healthcare provider with any questions you may have regarding a medical condition. Never disregard professional medical advice or delay in seeking it because of something you have heard in this podcast. The hosts, guests, and producers of this podcast are not responsible for any actions or inaction you may take based on the information presented in this podcast.

🏷️ Episode Tags

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Episode Transcription

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Hey, hello, everyone. This podcast is being brought to you today from the Center for Advanced

 

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Medicine just outside of Atlanta, Georgia. Please visit them at TCFAM.com. That's TCFAM.com.

 

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Dr. Stegall, thank you for being here in the studio with us today. I have been looking forward to this

 

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opportunity like you cannot believe. Me too, Robert. Thank you for having me.

 

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Dr. Stegall, for those that don't know who you are, please describe your background.

 

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From the very beginning, how you ended up getting into medicine, how you became an

 

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integrative oncologist, who were your mentors, who did you look up to? So many times

 

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a patient sees a doctor and they detach them from being a real human being.

 

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I think it's really important for people to understand who Dr. Stegall is.

 

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Sure. My story really starts when I was born. I was born almost three months prematurely.

 

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I obviously don't remember that, but I was always told as I grew up that I was a preemie.

 

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At that time, I weighed one pound and 14 ounces. At that time, it was about a 50-50 chance of

 

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survival. I was always told as I grew up that I was meant for something big and something special.

 

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I didn't know what I wanted to do when I was a kid. Obviously, with my life, I wasn't one of those

 

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kids that grew up and said, I want to be a doctor, I want to be a police officer. I didn't know,

 

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but I always remembered it was something important. Then when I was five years old,

 

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my grandmother was diagnosed with stage four stomach cancer. She was really the first

 

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relative I remember who had any sort of health issue, certainly cancer. I remember

 

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when she was diagnosed, my mom telling me that she had a tumor, which is like a growth,

 

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and that she would be having to undergo some pretty nasty treatments, some chemotherapy,

 

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radiation, things like that. That was going to affect the way grandma felt and the way she

 

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looked. She prepared me that grandma was going to lose some weight, lose her hair,

 

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probably not be herself. That was true. I remember, I always like to tell this story,

 

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but I remember when my mom took my grandma to buy a wig. She came home and had a wig for me too,

 

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and it was a clown wig. I still have that clown wig actually. I actually pulled it out the other

 

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day to look at it. I've saved it all these years, but I thought that was just kind of a sweet thing

 

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just to let me get a wig just like grandma got. But of course, as grandma went through treatments,

 

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she just declined. She lost a lot of weight, lost her hair, didn't feel good, nauseated,

 

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that kind of thing. She ultimately passed away. I just vividly remember how that took what was

 

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otherwise a really happy, healthy, seemingly healthy woman. He was very positive and upbeat.

 

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It wrecked her body, but it also just crushed her spirit. I remember being keenly aware of that,

 

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even at five years old, that grandma's different. That really made an impression on me. Then of

 

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course, growing up, I didn't really think much more about it. But then I really felt called

 

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toward medicine when I was in college. So I, again, wasn't exactly sure where life was going

 

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to take me. I was actually about to graduate with a business degree. I was just sort of praying about

 

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next steps. I thought business would be a good major, just whatever I did in life. God just put

 

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on my heart to be a doctor. That was not something I had really planned on. My mom was a doctor.

 

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She was an integrative family doctor. I was obviously exposed to that in a positive way,

 

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but going to medicine myself was just not something I had thought about. I just really felt

 

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called to that and kept praying about that. I just felt that was the right thing to do.

 

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So obviously I had to go back and take a whole bunch of classes I didn't get. A lot of science

 

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courses, organic chemistry, and biology, and physics, and all those things. But I did that

 

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and really just proceeded down the path of becoming a doctor. For those who are listening

 

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there's a lot of steps. There's courses. There's the MCAT test, which is a big test you have to

 

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take to get into medical school. I actually decided to do a master's degree in physiology.

 

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I thought it was going to be important for me just not having a science background as much to do that.

 

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My program was at Georgetown University. It was unique because they had a grant from the NIH to

 

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study alternative medicine. That was right up my alley because I knew when to go to medicine. I also

 

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had this appreciation for various alternative therapies. The program was very science-based

 

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in that we talked about physiology, and biochemistry, and all those things. But we also

 

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had courses in various alternative therapies, herbs, supplements, mindfulness, all kinds of

 

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different therapies. We were trained to examine those from a scientific perspective. We were

 

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trained specifically on how to evaluate the literature. As I went into medical school and

 

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my further training, I realized how important that is. You have to be able to look at a study

 

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and see is it a good study, who funded this study, was it a good population of patients,

 

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was it even done on people, or was it done on animals, was it done in the lab. There's a lot

 

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of things to have to think about in terms of research. I really got a great foundation in how

 

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do we evaluate research and decide if we think this is going to be good or not. Little did I know

 

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how important that would be for me in integrative oncology because as I go through my training to

 

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medical school, residency fellowship, again, I knew I wanted to incorporate integrative,

 

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but there's not a blueprint for that. There's not a standardized curriculum for integrative

 

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oncology. I had to create it as I went. To be able to look at the science for various things and

 

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decide whether they're worthy or not has been a really great skill to have.

 

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It's fantastic. What is your grandmother's name?

 

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Her name was Addie Lee. She's from here in the South. Addie Lee was her name.

 

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And your mother's name?

 

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My mom is Susan Stegall.

 

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I just want to honor them because they've had such an influence in your life in those early years.

 

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My mom, of course, she passed away a few years ago, but she was just an incredible influence on my

 

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life. That's fantastic to hear. Well, I'm certain that they are proud of you.

 

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Thank you. I hope so.

 

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For sure. You mentioned that it was Georgetown you were at, correct?

 

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For graduate school.

 

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That there was a grant, I think, some money for integrative

 

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complementary medicine.

 

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It was. They sponsored this graduate program specifically in physiology to study certain

 

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complementary alternative medicine therapies.

 

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And you said you had that that grabbed your interest. It sounded like you already had an

 

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interest. Where did that come from? Where did at that age? I mean, I'm just thinking most young

 

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people are not thinking that way, right? Of course, you're in medical school, but where did

 

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that come from?

 

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All right. That was my mom's influence. I grew up with integrative medicine in my house. So

 

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my mom had me taking supplements way before they were popular. My friends always thought it was so

 

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weird. Like, why are you taking pills and stuff? But I knew about that. I knew about supplementation,

 

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good nutrition. I was a health nut in terms of nutrition way before. Again, most people were

 

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talking about it. Just the importance of basic lifestyle things, exercise, hydration, sleep.

 

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I really grew up with all that. And then I saw my mom just have such success with patients with

 

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various health issues. And of course, she treated birth to death a whole lifespan. So she had

 

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little babies and toddlers. She had teenagers, adults, elderly. She really saw the whole spectrum

 

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of ages. And just hearing about her successes with patients using various integrative therapies was

 

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just a huge influence. And I thought, I have to incorporate this. I mean, I want to, I have to.

 

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To really help people.

 

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And she was a medical doctor also. You know, normally when we hear a medical doctor, we just

 

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think medicines. But here you are, you're growing up in a household where your mother, who's a medical

 

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doctor, is actually using supplementation. She's giving it to you. She's saying, hey,

 

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Jonathan, here's what you need to take this for.

 

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Right. Absolutely. Yeah.

 

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Okay.

 

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Yeah. And actually reaching for those things before she would reach for a medication. So I

 

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actually had that approach as well of, you know, maybe there are some natural things you can try

 

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for a certain ailment. And then if that doesn't work, we could always try a medication later.

 

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So it was, it obviously depended on the condition. But it wasn't reached for the

 

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pharmaceutical. And if that doesn't work, try something more natural. It was let's try something

 

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natural. If you think it's going to work well, then we'll go to something pharmaceutical if it doesn't.

 

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So that was always sort of my thought process.

 

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Wow. Now for those watching this right now are listening to it.

 

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Why doesn't that happen on a regular basis when I go to a doctor appointment?

 

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Conventional medical doctor. I think it's training. I think, you know, as I went through medical school,

 

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my mom hit on it one time. She said, you're having to flip your brain in a way as to learn everything

 

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you need to for medical school, because it's not the same way of thinking. It's very, you know,

 

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disease driven, symptom driven. It's not as much about how that disease is affecting that patient.

 

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And I think there's a subtle, there's a subtle difference, but it's a big difference. If we think

 

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about are we treating a disease or are we treating a patient who has a disease?

 

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And so when we look at it from a patient centric approach like that, I think it totally changes

 

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our paradigm. And so, you know, in medical training was outstanding. I mean, I think it's,

 

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I have a huge appreciation for Western medicine. I use it every day, but it leaves out a lot.

 

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And I think when we talk about what we're trained in, we're just trained in basically what the

 

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conventional medical model uses and what insurance approves. And so I think that really

 

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limits the toolbox when we're talking about a spectrum of therapies to choose from for patients,

 

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because it leaves out a whole lot of stuff that does have some good science behind it.

 

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It's just not part of that standard of care. And so doctors aren't taught about it.

 

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And then you to not get too much off on a tangent, but the other problem is doctors just don't have

 

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as much time as they would like with patients in general under that normal conventional medical

 

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model. And so not only do they not have the training in a lot of these other therapies,

 

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but they also don't have the time or interest to really go learn more about them either and

 

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to incorporate them. So it's a multifactorial problem, but it's out there. And I think unless

 

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you have a doctor who's willing to learn some of these things on his or her own and really step

 

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outside the box, it's just not, they're not going to know anything about it.

 

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Would it be fair to say that when a young doctor is coming out of medical school,

 

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and he's conventional doctor, taking medical insurance for payments, etc., versus like

 

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yourself, because you have a private practice, you don't take medical insurance.

 

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So is it fair to say that the doctor like yourself that's not taking medical insurance versus the one

 

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in a conventional practice that is that that contributes to having less time to continue to

 

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do further research? Absolutely. Absolutely. I mean, even for oncology, the average visit

 

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length is about 17 minutes. Now, can you imagine you're going in and maybe the visit is a little

 

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bit longer when you're seeing that doctor for the first time, maybe it's a little bit longer to talk

 

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about your diagnosis and treatments. But even imagine going through treatment, that's a pretty

 

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fast visit, 17 minutes, you're barely able to say hello and how you're feeling that day and

 

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answer a few questions and that 17 minutes is going to be up, especially if they're reviewing

 

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any sort of test results or anything like that. So I think that's a problem because

 

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doctors just aren't able to get the information that they need. I mean, one of the things I learned

 

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early on in medical school was if you talk to the patient, they'll tell you, they'll tell you their

 

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problem. They'll tell you they want to tell you. And we're trained to listen, we're trained to

 

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ask questions and then be quiet and listen. But then if you look at the research, doctors

 

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usually cut patients off after about eight seconds. So they asked you a question and then let the

 

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patient talk and then they interrupt them. And that's just not effective health care, as you know.

 

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And is that just happening because I got to get to the next patient?

 

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I think that's a lot of it. Okay. There's a lot of it. And I think there's also an arrogance to,

 

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I know what the problem is. I don't need to hear anymore. I mean, I think it's both, but I think

 

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it's largely just because doctors know they're seeing 30, 40, 60 patients that day and they need

 

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to eat on to the next one. When you consult with a patient doctor, on average, how long is that

 

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consultation? Our first consultation is usually at least an hour, hour and a half, sometimes even two

 

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hours. We spend a lot of time. And then, you know, even for follow-up visits, it's at least 30

 

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minutes, usually 30 to 45. That's fantastic. Yeah, especially when you have a health crisis

 

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that's what I would expect. I'd want to sit with my doctor for an hour. I'm in a health crisis.

 

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I got a cancer diagnosis here, right? Absolutely. That's fantastic to hear. So,

 

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I'm glad that we're bringing this up because every viewer listening to this needs to know that

 

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someone like a Dr. Stigalo as a private practice is not taking medical insurance for payments,

 

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has really the advantage to continue to do research, spend more time with the patient,

 

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which ultimately translates into a better quality of care for the patient.

 

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Absolutely. And I'm glad you brought that up because I think a lot of patients here

 

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that were not contracted with insurance and they say, oh, well, you know, why not? That's not very

 

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nice of you. Why wouldn't you take insurance? And it's not because we don't want to. It's,

 

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number one, because insurance doesn't cover a lot of these integrative therapies. And then, number

 

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two, like you said, we do want to spend more time with our patients. We don't want to be told by

 

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the insurance company, you can only bill for 10 minutes with this patient, 15 minutes. And that's

 

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how insurance companies do it. They say we bill for X, Y, and Z. And if you do that and the insurance

 

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covers that, that's great. But if you do anything outside of that, then you don't get paid. So,

 

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it's a really broken system because it's not about the patient. It's really not. It's about

 

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what insurance companies want to pay for. Yeah. I'm not going to put words in your mouth, but

 

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as far as I'm concerned, that's an immoral system. I mean, health is sacred. So, and the patient-doctor

 

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relationship is sacred as far as I'm concerned, but you cannot develop a level of intimacy with

 

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your doctor in eight minutes, not over health crisis. When you were in medical school, what

 

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was your biggest aha moment during medical school during that time? Well, during that time, I was

 

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again, sort of figuring out what specialty, what area, because you don't have to choose that up

 

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front. You choose that about the time you're graduating, you kind of choose, okay, here's

 

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a specialty I want to do. And I was just really drawn to cancer patients. So, I would go back

 

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after my work was done and I would just go visit with them. And it was really powerful the day I

 

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realized that I wasn't really able to help them much from a medical perspective. I mean, I had

 

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enough knowledge to know how to do the basics, but I knew for most of those patients, I was not going

 

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to get rid of their cancer. But I was able to at least be there for them just as someone who cared,

 

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someone who would listen, someone in a white coat, even though it was a short medical student,

 

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white coat, not a long attending physician, white coat, still just someone on the medical team who

 

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could listen to them, would care for them, would get on the glass of water, or whatever they needed.

 

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And so that was really my big aha moment. And as I went through more training and obviously became

 

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a physician and started managing patients myself, I still felt the same way. In medical school,

 

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I thought it was because I wasn't a doctor yet and because I was still learning. And once I had

 

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learned what they wanted me to learn, I still felt like I couldn't really help them. And that was one

 

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of my, okay, integrative oncology is where the answer has to be. How much of that was your

 

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grandmother? Probably a lot more than I've thought about. Probably. Yeah. More than I've realized.

 

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Yeah, absolutely. Wow. Okay. So when you finish medical school, you've made up your mind, you're

 

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going to be an integrative oncologist from the very beginning? Is that how you started from get-go?

 

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I was drawn to cancer. I didn't really know if I wanted to do that for sure yet. I initially just

 

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chose internal medicine because that's sort of a good base. You can stay in primary care

 

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or that's also the required step if you want to subspecialize. So if you want to do oncology,

 

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cardiology, critical care, whatever sort of specialty, you do internal medicine first. So

 

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I started with internal medicine residency and then while I was in internal medicine residency,

 

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I realized that I really felt called toward cancer specifically. Got it. Okay. Now,

 

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one of the things that has always struck me about Dr. Stegall is that I find you to be a researcher.

 

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You always seem to be dedicating time to looking at what is up and coming

 

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in the cancer field. What do I need to evaluate? Is there something up and coming that people

 

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should know or is there something that's intriguing you right now where you think there may be some

 

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significant hope here with this modality? Is there anything like that on the horizon?

 

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Well, there's a lot of stuff. I don't know how long you want me to talk on this, but

 

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to take a step back for a second, we always talk about the cure for cancer. We've been looking for

 

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it for decades. Going back to President Nixon declared war on cancer and we're going to develop

 

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all this research to cancer. We spent billions of dollars and we haven't found a cure. I think the

 

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reason for that is not because we're looking in the wrong place, but because it's not going to be

 

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one thing. There is not probably going to be one medicine we give to cure cancer. It's probably

 

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going to be a cocktail of things. It's going to be a combination. So in thinking of it like that,

 

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I think there are some things I'm excited about. We'll talk about chemotherapy later, I believe,

 

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but I'm still excited about chemotherapy. It does a lot. It's a powerful tool. But aside from that,

 

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I think immunotherapy is a really exciting field. We're learning about how to better harness the

 

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immune system so that it sees cancer better and fights it better. There's a lot of research with

 

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that. I think we're going to see a lot more good things coming from all the genetic research that's

 

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been going on lately too. We mapped the human genome a couple of decades ago, but we don't know

 

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what a lot of those mutations mean. But what we're finding is that we may be able to soon go in and

 

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target some of those mutations and repair them. And that's not going to mean anything we hear

 

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about the next year or two, but soon in terms of in the next 10, 20 years, we may be able to do that.

 

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And so I think that has obviously some potential pros and cons associated with it. But

 

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to be able to truly affect cancer on a genetic level is something that excites a lot of

 

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mainline cancer researchers. In terms of more supportive therapies, there continues to be more

 

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and more good data on nutrition, how important that is. We find most of the research leading

 

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us toward a more plant-based diet, obviously a concentration of fruits, vegetables, beans, grains.

 

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And then of course, you can debate over how much animal protein to add in there or things like that.

 

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But if plants are sort of the foundation, the bulk, if not all of the diet, then I think that's

 

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really going to be strongly anti-cancer. And then there's even some good data on the importance of

 

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when we eat. So it's not just what we eat, but when we eat. And so we're talking about things

 

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like fasting. There's a lot of good research coming out now on intentionally not eating for

 

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a certain period of time, whether that's part of a day or even several days straight. And all the

 

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good effects that that provides in the body. So I'm excited about a lot of it. It really depends

 

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on which area we're talking about. And all these things that you just mentioned, are they things

 

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that you're currently integrating with your patients right now at the Center for Advanced Medicine?

 

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Yes, other than obviously the genetic alterations. That's way down the road. But yes, I mean,

 

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I believe in a truly integrative approach where we're really taking the best of modern medicine,

 

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chemotherapy, immunotherapy, surgery, but integrating that with a lot of good natural

 

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alternative therapies as well. That's really to me where the magic happens. Because we have a

 

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bigger toolbox that way. We're not limiting ourselves like a conventional oncologist or

 

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even someone who's strictly alternative in their approach. They're missing a lot of other tools

 

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they could be using. Okay, got it. Now, I know you're an author, you have a book called Cancer

 

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Secrets. And you also have your own podcast. You have your own website dedicated to this,

 

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which is fantastic. It answers so many frequently asked questions for patients. So thank you for

 

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investing the time. I really appreciate that. Let's talk about chemotherapy because when

 

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patients hear you have cancer, you got cancer, immediately treatments kicks into their mind.

 

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And that's going to be chemo or radiation, maybe a surgery. You mentioned the story about your

 

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grandmother and how your own mother prepared you for the physical changes that were going to take

 

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place. And they did take place. And this is the image that we all have in our minds about

 

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chemotherapy. It's like, I think for most of us, we think this is a bomb that's going to get dropped

 

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on me. Please explain to our viewers why we don't need to be afraid of it in that kind of way. Give

 

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us a history of chemotherapy. Explain to us how you leverage this tool because I think you mentioned

 

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in your book, hey, we got a toolbox here. And this is a major tool that shouldn't necessarily

 

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be abandoned but used differently. Right. Right. So the history of chemotherapy is

 

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you know, decades old. I mean, it goes back to the 1950s. When chemo was first used, there was a

 

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certain type of pediatric cancer, I believe it was a lymphoma that they found actually responded

 

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well to a derivative of mustard gas. And so the joke is that chemotherapy is mustard gas. But

 

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obviously it's evolved a lot since then. But they obviously had to play with the dosing and the

 

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frequency and everything with that regimen. But the approach at that time was these are kids who

 

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have a horrible diagnosis. Let's give them as much of this drug as they can stand because we want to

 

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make sure we get rid of it. And so the whole concept of what's called maximum tolerated dose

 

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chemotherapy, we sometimes abbreviate that MTD for maximum tolerated dose. That's what came about.

 

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And interestingly, as more and more chemo drugs were developed, the whole concept of MTD chemotherapy

 

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remained. And so that's what you see today. If you go into any conventional oncology office,

 

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they're going to dose the patient using a maximum tolerated dose approach. And that's basically

 

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taking the patient's height, the patient's weight, and then establish dosing guidelines for that

 

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particular chemo agent. And that's what the patient gets. And they know they can only give it once every

 

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two or three weeks, typically, sometimes some can be given once a week. But typically there's a two

 

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or three week break from one dose to the next because the patient couldn't safely tolerate more

 

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than that. And now when we talk about maximum tolerated dose, we're not just saying the patient

 

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will have side effects. Obviously they will. It's more like how much can we give the patient not to

 

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put them in the hospital with some degree of certainty. So we know that we're still probably

 

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going to wipe out their immune system. We're going to probably cause some anemia, maybe

 

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affect their kidneys or their liver. Obviously that can cause a lot of side effects, whether it's

 

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nausea, vomiting, diarrhea, rashes, whatever it may be. So that is what we associate with chemotherapy,

 

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especially if we've had a relative maybe go through that or maybe some of our listeners are

 

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going through that themselves. And that makes me sad because to me, chemotherapy is just a tool.

 

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And I would argue that we've been using it the wrong way all these years. If you think about

 

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maximum tolerated dose, I would rather think about it in terms of minimum effective dose. So what's

 

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the least we can use to still get the effect we want? And chemo is just like any other tool,

 

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Robert. Is it being used in the right hands by the right person? And is it being used

 

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responsibly? It's like a car. You can get behind the wheel of a car. You can go 200 miles an hour

 

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and you can cause a fatality. And if everyone did that, we would probably say that cars are dangerous.

 

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But because we know how to use cars and how to drive them safely, they still get us where we need

 

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to go. But they're generally recognized as safe. We can use a lot of examples to illustrate that.

 

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But I think chemo is just so effective. I know it is. We just need to use it better.

 

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And so what I really found to work in my practice is called fractionated metronomic chemotherapy.

 

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And that's basically a long way of saying that we're using lower doses of chemo and we're giving

 

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it more often. And there's good research to support this. There's research showing that these lower

 

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doses given more often work really well because it actually keeps a nice steady level of chemotherapy

 

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in the body all the time. And that may sound scary to some people, but from a cancer treatment

 

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perspective, that's a good thing because the problem we run into with these big doses that

 

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are given with a big gap in therapy is there's a long period of time where that chemotherapy is not

 

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in the blood at all. And that gives the cancer cells that are still there a wonderful opportunity

 

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to mutate so that treatment doesn't affect them later. And so we have this concept of resistance

 

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that we talk about a lot, cancer cell resistance. And that really breeds resistance when we're

 

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given that big dose of chemo and then we have to wait all that time to give another dose. So with

 

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the lower dosing more often, so instead of giving one dose every two or three weeks, we're giving

 

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these small doses three times a week, for example, it keeps a nice steady level so that cancer

 

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doesn't have a chance to adapt. So we should get more longevity out of that treatment.

 

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But with the lower dosing, we're avoiding a lot of those side effects that patients associate

 

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with chemo. So it's not to say you can't have any side effects because everybody's different,

 

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but the risk of the hair loss, nausea, vomiting, fatigue, all those horrible chemo symptoms,

 

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the risk of that is just so much lower. So I found it to work really well. And that's why I view

 

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chemotherapy as a really powerful tool to the point that if someone's recommended to have

 

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chemotherapy and they don't do it, they're really missing a huge opportunity to treat their cancer

 

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better. So I want everyone to know that, that if you're supposed to have chemo and you're choosing

 

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not to, that you're making it a lot harder on yourself if you don't do it.

 

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Okay. When you talk about these fractionated doses that are lower, earlier you mentioned the

 

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maximum tolerated dose based on height, weight. So is a fractionated dose also based upon height

 

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and weight in a percentage or what does that look like?

 

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It is. Great question. So we still take that maximum tolerated dose calculation,

 

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but then we take a percentage of that. So if we call the maximum tolerated dose 100%,

 

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then we usually give about 10 to 15% of that, sometimes 20%. So we're a much lower dose than

 

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the normal. But the way that's metabolized by the body, I think it worked really well.

 

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And so they're getting that two to three times a week.

 

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We typically do three. Yeah.

 

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Okay. For how many weeks?

 

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We typically do it in a four week block. So over that four weeks, they're going to get,

 

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you know, about 12 treatments. And then we found that it's important to take a break at that point.

 

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We've played with various lengths of treatment. We've tried six weeks, we've tried three weeks,

 

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and we found that the four week amount of time is really a good amount of time. If you go beyond

 

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that, you can start to see it wear on the patient a little bit more. So we take a break and we

 

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typically put the patient on some kind of oral chemotherapy, usually a low dose, for about a

 

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four week period. And then we'll come back and do more, another four weeks of the IV chemotherapy.

 

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So in the context of my office, we do a 12 week treatment program, four weeks in the office with

 

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IV chemo, four weeks at home with an oral chemo, and then four weeks back in the office with an

 

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IV chemo again, along with a lot of other therapies, obviously. Sure. So about a three

 

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month commitment on the part of the cancer patient themselves. But really a small commitment of time

 

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when you think about the health crisis, right? Right. The picture that we're in here. As far as

 

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those fractionated doses over a period of four weeks, and the accumulation, the fact that it's

 

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staying in the body, is this accumulating to what full dosages would look like over a period of time?

 

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Or is it just, I know nothing about biology the way you do. So what is happening in the human body

 

332

00:28:25,520 --> 00:28:28,880

during this time? Yeah, that's a great question. So a lot of patients do like to say, okay, well,

 

333

00:28:28,880 --> 00:28:34,240

how many of these small doses will equal a full dose? That's an understandable question. But really,

 

334

00:28:34,240 --> 00:28:39,920

the way these drugs are metabolized and broken down in the body, it's not exactly the same because

 

335

00:28:40,000 --> 00:28:45,200

we also have metabolites of these drugs that are doing some work for us as well. So if you look at

 

336

00:28:45,200 --> 00:28:51,120

the what's called a half life of a lot of these medications, many of them are hours or a day or

 

337

00:28:51,120 --> 00:28:55,600

so, a day or two. So a lot of that drug is actually going to be metabolized out even a couple days

 

338

00:28:55,600 --> 00:28:59,520

later for most of these chemo agents. So that's why we feel like it's safe to go ahead and give

 

339

00:29:00,240 --> 00:29:04,320

another dose again. So it's a little bit different because the body is metabolizing that and there's

 

340

00:29:04,320 --> 00:29:09,440

a lower level and then we hit it again. So it's not exactly the same as saying, you know, 10 doses

 

341

00:29:09,440 --> 00:29:13,520

at 10% of the full dose is the same as one full dose. It's not, I think about it differently than

 

342

00:29:13,520 --> 00:29:17,680

that. Okay, you just mentioned a word half life for those that have never heard that explain it

 

343

00:29:17,680 --> 00:29:24,320

to us. So half life is the amount of time it takes for half of an active component of a medication

 

344

00:29:24,320 --> 00:29:29,600

to be broken down in the body. So the, we primarily think of the liver doing that. The kidneys are

 

345

00:29:29,600 --> 00:29:33,760

involved in the metabolism of some drugs as well. But basically, if you start with 100 milligrams,

 

346

00:29:34,480 --> 00:29:38,960

if the half life is four hours, then after four hours, you'd have 50 milligrams left.

 

347

00:29:39,520 --> 00:29:43,680

And then, you know, of course, that same period of time half life, you'd have it again. So it's

 

348

00:29:43,680 --> 00:29:47,920

different for different medications. And the nice thing about these drugs, they've all been studied

 

349

00:29:47,920 --> 00:29:52,240

in detail to know exactly how they're going to work in the body. We know what to expect in terms

 

350

00:29:52,240 --> 00:30:01,280

of not only how they work, but how long they work. When patients hear chemotherapy, some, not all,

 

351

00:30:01,280 --> 00:30:07,440

but some think to themselves, it's all the same. But how many actual chemotherapy agents exist in

 

352

00:30:07,440 --> 00:30:12,480

the world today? I mean, is there is there over 100 of these things that exist? Yeah, there are a

 

353

00:30:12,480 --> 00:30:17,760

lot. I mean, there's there's certainly dozens. There probably are over 100 total. There are a

 

354

00:30:17,760 --> 00:30:22,000

lot. So they all work a little bit differently. So that's the other thing you people need to realize

 

355

00:30:22,000 --> 00:30:25,760

is, you know, chemotherapy typically works on the nucleus of a cancer, that's where the DNA and the

 

356

00:30:25,760 --> 00:30:31,120

RNA, all those important genetic components are. So chemo works on those. But there's different

 

357

00:30:31,120 --> 00:30:35,440

areas of that DNA or RNA that are being targeted by the chemo. And so that's why we usually like to

 

358

00:30:35,440 --> 00:30:40,320

use two or three different chemo agents at the same time to attack that cancer cell differently.

 

359

00:30:41,040 --> 00:30:46,880

So they all work a little bit differently. And some chemos are even derived from plants. I like

 

360

00:30:46,880 --> 00:30:52,240

to tell patients that they think all chemo is just made in some lab by some evil drug company. Well,

 

361

00:30:52,240 --> 00:30:56,080

a lot of them did are derived from plant active ingredients are obviously purified

 

362

00:30:56,880 --> 00:31:00,880

in concentrated in the lab, but they are kind of plant based in a way.

 

363

00:31:00,880 --> 00:31:07,680

Okay, got it. So when you do these fractionated doses, you're using two to three chemos within

 

364

00:31:07,680 --> 00:31:15,120

the same infusion? Okay, same treatment time. And these three combined are equating to the 10 to 15

 

365

00:31:15,920 --> 00:31:22,960

of the full dose. So they're each 10 to 15% of a full dose for that agent. So chemo A 10 to 15%

 

366

00:31:22,960 --> 00:31:29,520

of the full dose for that chemo B 10 to 15% chemo C 10 to 15%. So they're all 10 to 15% of the full

 

367

00:31:29,520 --> 00:31:35,520

dose given one after the other at the same treatment session. Okay, so they're not all in

 

368

00:31:35,520 --> 00:31:40,400

the same bag. They're no they're pushed separately. Okay, depending on the chemo, sometimes they can

 

369

00:31:40,400 --> 00:31:44,720

be given through an IV, you know, push and then other times they have to be dripped in. But they're

 

370

00:31:44,720 --> 00:31:50,880

given sequentially. Okay, that's good to know. Now, with all these chemotherapy agents that exist,

 

371

00:31:51,840 --> 00:31:59,680

in conventional oncology, are there like go to chemotherapies for certain cancers? In other words,

 

372

00:31:59,680 --> 00:32:04,640

if you have breast, this is the go to chemotherapy we want. If you have pancreatic cancer, this is

 

373

00:32:04,640 --> 00:32:09,920

the go to. Does that exist like that? It does. And we rely heavily on that because the the research,

 

374

00:32:09,920 --> 00:32:15,280

we let the research guide us if we have three or four chemos that we know are sort of the first

 

375

00:32:15,280 --> 00:32:19,680

line. Most the most studies seem to be the best effective for a certain cancer, then that's

 

376

00:32:19,840 --> 00:32:24,480

typically what we start with. And we found that to work well, very well with our methods as well.

 

377

00:32:24,480 --> 00:32:29,200

So we do rely on the research in that way. There are some some various tests that can be done to

 

378

00:32:29,200 --> 00:32:34,080

maybe help clarify that. But we found those are usually aren't needed. Usually we can go with what

 

379

00:32:34,080 --> 00:32:40,000

the research shows. Okay, great. Now, I know with these chemotherapy agents, there's material safety

 

380

00:32:40,000 --> 00:32:46,080

data sheets for these, right? That tells you about their side effects, etc. But those would be based

 

381

00:32:46,080 --> 00:32:53,040

upon full dosage, correct? Correct. Correct. So that's assuming a full dose. So a lot of times

 

382

00:32:53,040 --> 00:32:58,000

when I talk to patients about my chemotherapy recommendation, they go online and they start

 

383

00:32:58,000 --> 00:33:02,000

reading about it. And they say, Dr. Stegall, there's 50 side effects I could be getting from this. I'm

 

384

00:33:02,000 --> 00:33:05,920

not sure I want to do this. And I tell them that, you know, there's certainly they're there for a

 

385

00:33:05,920 --> 00:33:10,400

reason. But typically, that's associated with a full dose and doesn't necessarily apply with a

 

386

00:33:10,400 --> 00:33:15,920

lower dose. Right. And obviously, there are paid studies to demonstrate what a low dose side effect

 

387

00:33:16,560 --> 00:33:24,880

is. Okay. Okay, got it. Now, talk to us a little bit about how you deliver this fractionated

 

388

00:33:24,880 --> 00:33:29,680

dose because that's different. You know, we just discussed lower dosages. But how is it getting

 

389

00:33:29,680 --> 00:33:34,640

delivered at Center for Advanced Medicine? Right. Good question. So one of the issues with

 

390

00:33:34,640 --> 00:33:40,960

chemotherapy is that it only targets what we call actively dividing cancer cells. So if you can

 

391

00:33:40,960 --> 00:33:47,040

imagine within a tumor, it's pretty chaotic. All the various cancers, let's say there's a million

 

392

00:33:47,040 --> 00:33:51,920

cancer cells in that tumor, which sounds like a lot, but it's actually not. I mean, there can be

 

393

00:33:51,920 --> 00:33:57,520

many millions of cancer cells within a tumor. Some are going to be growing and dividing, which is

 

394

00:33:57,520 --> 00:34:03,120

what cancer likes to do. It likes to grow and divide so that it can continue to spread. But some

 

395

00:34:03,120 --> 00:34:06,160

of those cells are going to be dormant. They're not going to be growing or dividing. They're going to

 

396

00:34:06,160 --> 00:34:11,440

be basically asleep. And these cells can go in and out of growth and division and dormancy

 

397

00:34:13,280 --> 00:34:18,480

all day. I mean, it just depends on when you give that chemo, you're going to target the ones that

 

398

00:34:18,480 --> 00:34:21,440

are growing and dividing. But if they're not dividing, then you're not going to hurt them.

 

399

00:34:22,080 --> 00:34:25,200

And that's one of the real problems with conventional cancer treatment is, you know,

 

400

00:34:25,200 --> 00:34:29,440

let's say you're giving that big full dose once every two weeks. Well, you're probably going to

 

401

00:34:29,440 --> 00:34:32,800

kill the cells that are dividing, but what about the ones that weren't? And then you know, you're

 

402

00:34:32,800 --> 00:34:36,000

going to have to wait two more weeks before we can try again and just hope that some of those

 

403

00:34:36,000 --> 00:34:44,400

other cells are vulnerable. So one of the things that we do is really try to have as many actively

 

404

00:34:44,400 --> 00:34:48,400

dividing and therefore vulnerable cancer cells at that time of chemotherapy. So it's under our

 

405

00:34:48,400 --> 00:34:53,680

control, our supervision, but we want that because that's going to make our dose go farther if we can

 

406

00:34:53,680 --> 00:34:58,480

have more vulnerable cancer cells at the time. So the first thing we actually do is we have patients

 

407

00:34:58,480 --> 00:35:03,280

fast before chemotherapy. That's really important. So studies have shown that a fast leading up to

 

408

00:35:03,280 --> 00:35:08,160

chemotherapy helps it work better. It also reduces side effects. And so that was shown in

 

409

00:35:08,160 --> 00:35:12,960

conventional literature and conventional oncology. So we apply that to our method as well. We usually

 

410

00:35:12,960 --> 00:35:16,800

have patients stop eating eight or nine o'clock the night before treatment. So they come in in

 

411

00:35:16,800 --> 00:35:22,320

the morning, they've been fasting for about 12 hours usually, give or take. That's going to help

 

412

00:35:22,320 --> 00:35:27,440

prime the environment. And if you think about it, you know, cancer is so energy driven. It has

 

413

00:35:28,320 --> 00:35:34,720

a significant increase in the glucose or sugar receptors on its surface. They have a lot more of

 

414

00:35:34,720 --> 00:35:39,840

a need for insulin because they're so active. They're growing so much faster than a normal

 

415

00:35:39,840 --> 00:35:44,400

healthy cell would. And so we take advantage of that. And so we use something called insulin

 

416

00:35:44,400 --> 00:35:50,080

potentiation therapies, sometimes abbreviated IPT. And what that entails is we actually give insulin,

 

417

00:35:50,080 --> 00:35:54,560

and I'm sure everyone knows that insulin is a diabetes drug. It is designed to lower blood

 

418

00:35:54,560 --> 00:36:01,520

sugar. But we actually give insulin to activate as many of those dormant cancer cells at the time

 

419

00:36:01,520 --> 00:36:06,880

of treatment as possible. So we have a much greater population of vulnerable cancer cells.

 

420

00:36:06,880 --> 00:36:12,640

And so what that looks like is we actually have a patient come in fasting, we give them

 

421

00:36:13,360 --> 00:36:20,480

IV dextrose, IV sugar, we raise their blood sugar, and we then give insulin to lower that blood sugar

 

422

00:36:20,480 --> 00:36:27,520

back toward normal. And we found that that works really well. We used to actually do it the opposite.

 

423

00:36:27,520 --> 00:36:33,360

We used to lower the blood sugar first, lower them down below normal, which which wasn't very

 

424

00:36:33,360 --> 00:36:37,840

comfortable for some patients. And then we give some sugar to raise it back to normal. But we found

 

425

00:36:37,840 --> 00:36:41,120

that if we raise the blood sugar first, we can actually give more insulin because insulin is the

 

426

00:36:41,120 --> 00:36:45,280

driver of this whole thing. The sugar helps sort of buffer the insulin to make sure the blood sugar is

 

427

00:36:45,920 --> 00:36:52,400

behaving like we want it to. But the insulin is really what we feel is driving this process to

 

428

00:36:52,400 --> 00:36:58,320

sort of activate those cancers over the time of treatment. So we do that. And really the patient

 

429

00:36:59,120 --> 00:37:03,120

doesn't really feel anything. I mean, there's not going to be lightheadedness or chills or any of

 

430

00:37:03,120 --> 00:37:06,720

that like you'd see with low blood sugar. When a patient has a high blood sugar, it's like you just

 

431

00:37:06,720 --> 00:37:12,400

had a nice big meal, right? You're not going to feel badly. And so we found it to be very safe.

 

432

00:37:12,560 --> 00:37:16,400

We're checking blood sugar regularly. So even though we're manipulating the blood sugar a little

 

433

00:37:16,400 --> 00:37:21,760

bit, we're very careful to make sure that it's falling within the parameters that we are looking

 

434

00:37:21,760 --> 00:37:30,480

for. And that's it. And the chemo's go in during that time while we're delivering the insulin and

 

435

00:37:30,480 --> 00:37:35,840

the dextrose once they've taken effect. And so it's a really easy well-tolerated procedure.

 

436

00:37:36,720 --> 00:37:41,200

That's how we give chemo. And we do that every time we give chemo. So Monday, Wednesday, Friday,

 

437

00:37:41,200 --> 00:37:45,840

in my practice, that's how we do it. IPT with chemo. Perfect. Perfect. Thank you for that

 

438

00:37:45,840 --> 00:37:50,800

explanation. So Dr. Stegall, when it comes to giving the patient insulin, I want to make sure

 

439

00:37:50,800 --> 00:37:58,160

I heard this correctly. One of the key purposes is that there's dormant cancer cells that are not

 

440

00:37:58,720 --> 00:38:03,440

dividing. Right. All right. So you give the insulin to make these dormant cells

 

441

00:38:04,480 --> 00:38:10,880

wake up as it were. Are they dividing at this time? Is that the theory? Yes. That they're

 

442

00:38:10,880 --> 00:38:16,480

growing in preparation or actively dividing when we give chemo. That makes them vulnerable.

 

443

00:38:16,480 --> 00:38:24,240

Okay. So then when you deliver the glucose, which follows next, which they're hungry for,

 

444

00:38:24,240 --> 00:38:30,800

exactly. Right. It's kind of like Pac-Man. Right. They're coming to consume it. Then you follow it

 

445

00:38:30,800 --> 00:38:38,400

up with the fractionated chemotherapy. So they're consuming that. The idea is in theory that those

 

446

00:38:38,400 --> 00:38:42,640

fast dividing cells are all, there's more of them now because they were dormant and they're

 

447

00:38:42,640 --> 00:38:48,560

consuming that chemotherapy and you're killing cancer cells at that point. Bingo. Okay. And

 

448

00:38:48,560 --> 00:38:53,440

minimizing the side effects at the same time. Right. All right. It's fantastic. It's good news.

 

449

00:38:54,480 --> 00:39:02,160

What are you integrating with IPT to make it work better? Because obviously there's other things

 

450

00:39:02,160 --> 00:39:07,600

that you're doing. You mentioned it earlier. You're an integrative oncologist. Right. What have you

 

451

00:39:07,600 --> 00:39:18,000

found to be very successful? We found that hyperthermia, which is heat, applied to a specific

 

452

00:39:18,000 --> 00:39:22,800

area. So we call that local hyperthermia versus a global hyperthermia would be basically heating

 

453

00:39:22,800 --> 00:39:26,800

the patient, giving them a fever. We don't want to do that. But local hyperthermia, we're able to

 

454

00:39:26,800 --> 00:39:33,920

place a pad, especially designed hyperthermia pad over a certain area is important because that is

 

455

00:39:33,920 --> 00:39:39,360

going to do a few things. Number one, it's heat kills cancer. So cancer doesn't withstand heat as

 

456

00:39:39,360 --> 00:39:43,920

well as a normal healthy cell would. And so we know that there's going to be a cancer cell killing

 

457

00:39:43,920 --> 00:39:48,080

effect from the heat. It's going to recruit some immune cells to the area being heated, but probably

 

458

00:39:48,080 --> 00:39:53,520

most importantly, heat is going to bring a little bit extra blood flow to an area. So if you can

 

459

00:39:53,520 --> 00:39:58,560

imagine the timing we're giving chemotherapy, there's blood in the chemotherapy. It's going to

 

460

00:39:58,560 --> 00:40:02,800

circulate around. Let's divert a little bit of that blood to the area of greatest concern for the

 

461

00:40:02,800 --> 00:40:08,320

patient. If they have a breast mass, we'll put the hyperthermia device over their breast and bring a

 

462

00:40:08,320 --> 00:40:12,240

little bit more chemotherapy-rich blood to that area. Or if it's over the liver, we're going to

 

463

00:40:12,240 --> 00:40:17,520

put some heat over that area. And we found that to work well because obviously the chemo is still

 

464

00:40:17,520 --> 00:40:21,680

going to be systemic and we want it to be, right? Because who knows where cancer cells might be,

 

465

00:40:22,560 --> 00:40:26,640

but we know if there's a certain area to prioritize that the hyperthermia is going to help us do that.

 

466

00:40:27,680 --> 00:40:32,240

And the nice thing about this device is it's not going to burn the skin. A lot of the older

 

467

00:40:32,240 --> 00:40:37,120

hyperthermia devices would actually burn the skin because most of the heat is there versus this

 

468

00:40:37,120 --> 00:40:42,800

actually causes the heat to collect under the skin to a certain extent. So we're able to heat an area

 

469

00:40:42,800 --> 00:40:49,040

below the surface and really spare the skin from the burns. So we found that to work really well

 

470

00:40:49,040 --> 00:40:56,480

to integrate with chemo and IPT. And the local hyperthermia is being done prior to the fractionated

 

471

00:40:56,560 --> 00:41:02,880

chemotherapy through IPT. Yes, we apply the heat, let that get to a certain temperature,

 

472

00:41:02,880 --> 00:41:08,000

and then that's when we start our chemo, when we know that there's already the heat in that area.

 

473

00:41:08,000 --> 00:41:14,000

Got it. So as I'm putting this together and correct me if I'm wrong, when I think about the IPT and

 

474

00:41:14,000 --> 00:41:21,280

you give insulin to the patient to wake up those dormant cells, as it were, you're really creating

 

475

00:41:21,840 --> 00:41:29,120

like a magnet in the body to receive the chemo. But by applying the local hyperthermia beforehand,

 

476

00:41:29,120 --> 00:41:32,560

now you're making it a super magnet where the tumor is.

 

477

00:41:32,560 --> 00:41:37,760

Right. Exactly. If it's more concentrated to a tumor, as well as more likely to be taken up by

 

478

00:41:37,760 --> 00:41:42,960

cancer cells, that's going to be less chemo that can go to places we don't want it to go. So we

 

479

00:41:42,960 --> 00:41:46,720

think about collateral damage and only are we addressing that with a lower dose. But if we're

 

480

00:41:46,720 --> 00:41:52,240

targeting the chemo better, the chances of a lot of these other untoward side effects is going to

 

481

00:41:52,240 --> 00:41:57,360

be a lot lower. I'm sure there was a time where you were not using local hyperthermia in the practice,

 

482

00:41:58,800 --> 00:42:04,560

but you were using IPT, fractionated doses. So from the time that you weren't doing this to

 

483

00:42:04,560 --> 00:42:07,920

the time that you are now, you're actually doing, what was the difference that you noticed with the

 

484

00:42:07,920 --> 00:42:14,880

patients? I definitely noticed an improvement in the reduction of tumors. I mean, I certainly

 

485

00:42:14,880 --> 00:42:19,520

got good results before, but I do feel like it's increased the results. Especially,

 

486

00:42:19,520 --> 00:42:24,720

the really neat thing is seeing patients that have tumors that are visible. So some patients will

 

487

00:42:24,720 --> 00:42:30,080

come to us, they'll have a breast mass that's come through the skin that's exposed or something like

 

488

00:42:30,080 --> 00:42:36,560

that. And you really can literally watch those get smaller over the course of weeks of treatment.

 

489

00:42:36,560 --> 00:42:40,800

And so it's pretty cool to see. And obviously we monitor labs and imaging as well. So if it's an

 

490

00:42:40,800 --> 00:42:44,720

internal tumor, we still are going to see that too. But it's neat to see that as we go along,

 

491

00:42:44,720 --> 00:42:50,320

to actually see the effect of the treatment. And I have seen an increase in those benefits

 

492

00:42:50,320 --> 00:42:56,960

just since we included the hyperthermia. Fantastic. With the insulin, and I know I'm

 

493

00:42:56,960 --> 00:43:04,560

going back here just for a minute, but it just dawned on me. Is there any risk of insulin causing

 

494

00:43:04,560 --> 00:43:09,040

the cancer to spread because those dormant cells are not coming to life? In other words,

 

495

00:43:09,520 --> 00:43:14,480

is it possible through the insulin that over a period of maybe four weeks or eight weeks later,

 

496

00:43:14,480 --> 00:43:20,000

that there could be more cancer cells that are dividing and spreading? Is there a risk of that

 

497

00:43:20,000 --> 00:43:24,800

at all? That's a great question. So we don't have any research showing that that accelerates the

 

498

00:43:24,800 --> 00:43:33,120

growth of and spread of cancer. Now, I view it more as, if you have cancer, anytime you eat,

 

499

00:43:33,120 --> 00:43:36,400

potentially you're going to fuel cancer, right? That's just the reality of it because cancer is

 

500

00:43:36,400 --> 00:43:42,560

relying on those same nutrients and other things that normal healthy cells are. So we know that

 

501

00:43:42,560 --> 00:43:49,040

anytime we give any sort of fuel, it could cause cancer to grow. But because we're doing it under

 

502

00:43:49,040 --> 00:43:55,840

our supervision at the time of treatment, I don't have any concerns about that. Now, we do know from

 

503

00:43:55,840 --> 00:44:01,280

the research that the diabetics get more cancer and they have worse outcomes from cancer than

 

504

00:44:01,280 --> 00:44:05,760

people who don't have diabetes. So part of that is because they don't have as good a blood sugar

 

505

00:44:05,760 --> 00:44:11,440

control and part of that is quite possibly because of insulin. But because we're doing it in a

 

506

00:44:11,440 --> 00:44:17,520

controlled setting, limited times, and we're talking about giving, of course, of a three-month

 

507

00:44:17,520 --> 00:44:24,160

treatment program, it's 23 chemotherapies that we give, IV chemo. And so it's 23 times you're

 

508

00:44:24,160 --> 00:44:29,360

getting insulin. That's not significant at all. Whereas if we were obviously giving it every day

 

509

00:44:29,360 --> 00:44:34,960

for 10 years, maybe that could cause some issues. But because it's under our control at the time of

 

510

00:44:34,960 --> 00:44:38,400

treatment, we know we're giving chemotherapy. I have no concerns about that. Okay. And there's a

 

511

00:44:38,400 --> 00:44:43,840

really targeted approach that you're describing. Absolutely. Okay. One of the things that

 

512

00:44:45,520 --> 00:44:51,600

you mentioned earlier in conventional medicine was that there are dormant, these dormant cells,

 

513

00:44:51,600 --> 00:44:58,720

these dormant cancer cells, and the chemotherapy will develop a resistance. And so I'm thinking

 

514

00:44:58,720 --> 00:45:06,400

of myself, I think we've all met a cancer patient that had conventional chemotherapy,

 

515

00:45:06,400 --> 00:45:11,840

and maybe even integrative. I don't know, but it has come out and said, I'm cancer-free.

 

516

00:45:14,080 --> 00:45:22,080

Only to have the cancer reappear in three months or six months or 12 months, they obviously,

 

517

00:45:22,080 --> 00:45:26,800

it's great to hear those words, you're cancer-free. However, that was determined. But

 

518

00:45:27,280 --> 00:45:32,720

if there's dormant cells, I mean, should we be telling patients this? I mean,

 

519

00:45:33,440 --> 00:45:38,720

or when should we tell patients they're cancer-free? What's your opinion on this?

 

520

00:45:38,720 --> 00:45:43,120

Yeah, I agree. We throw around cancer-free cure. We throw on those words a lot. I actually don't

 

521

00:45:43,120 --> 00:45:48,080

use them in my practice. I will say that there is no evidence of disease, no evidence of cancer,

 

522

00:45:48,080 --> 00:45:52,800

but I can't guarantee that there's not a cancer cell in there somewhere. Even with the advanced

 

523

00:45:52,800 --> 00:45:56,800

testing that we incorporate, it's great when that test doesn't show any evidence of cancer,

 

524

00:45:56,800 --> 00:45:59,920

but that doesn't mean there couldn't be something there that could pop up later.

 

525

00:45:59,920 --> 00:46:05,360

That's why the monitoring is so important. How often should people monitor themselves

 

526

00:46:05,360 --> 00:46:12,320

and monitor themselves with what test? So patients who have cancer, I'm really big on

 

527

00:46:12,320 --> 00:46:16,560

getting your information. I always say, if we don't know our enemy, we can't fight it well.

 

528

00:46:16,560 --> 00:46:26,000

Cancer is a formidable adversary, right? I mean, we know it can take over the body if we let it.

 

529

00:46:27,920 --> 00:46:33,440

On a very basic level, this may be common sense to our listeners, but get a biopsy. If you think

 

530

00:46:33,440 --> 00:46:37,200

you might have cancer, get the biopsy. There's all kinds of stuff on the internet about biopsies

 

531

00:46:37,200 --> 00:46:42,240

spread cancer, and they're dangerous, and they don't. So get your biopsy. You need to know,

 

532

00:46:42,240 --> 00:46:45,600

first of all, whether it's cancer or not, but then also that's going to give us some extra

 

533

00:46:46,160 --> 00:46:51,600

information on that tumor. If it is cancer, let's say it's breast cancer, well, is estrogen driving

 

534

00:46:51,600 --> 00:46:57,120

that cancer or not? Is progesterone driving that cancer? We can do all kinds of studies now on that

 

535

00:46:57,120 --> 00:47:04,480

tumor tissue to actually see how it's behaving and whether that gives us different treatment options.

 

536

00:47:05,200 --> 00:47:12,800

But then beyond that, I do use the conventional tumor markers, things like the CA125 or CA153

 

537

00:47:12,800 --> 00:47:17,520

or PSA, things like that. I think they're important to monitor as you go through cancer,

 

538

00:47:17,520 --> 00:47:21,600

just to see how those respond. I don't think they're perfect. Those are just proteins that

 

539

00:47:21,600 --> 00:47:27,680

we measure, and they can be elevated for other reasons as well. So I do think imaging plays an

 

540

00:47:27,680 --> 00:47:32,400

important role. No one wants to be exposed to radiation, but a PET CT scan is kind of the gold

 

541

00:47:32,400 --> 00:47:38,320

standard. So I do think that's important to get a PET scan or even just a CT or MRI. Just depending

 

542

00:47:38,320 --> 00:47:42,720

on the cancer type, we decide what's appropriate. But a picture is worth a thousand words, and

 

543

00:47:42,720 --> 00:47:48,080

a lab test won't necessarily show you everything you need to know. So I think imaging at regular

 

544

00:47:48,080 --> 00:47:52,560

intervals is important. Then I'm also using a test right now called Signatera that I really like a

 

545

00:47:52,560 --> 00:47:59,680

lot. It actually takes a sample of the patient's tumor tissue, and that can be previously obtained

 

546

00:47:59,680 --> 00:48:06,160

from biopsy or surgery. The pathologist at Signatera will come up with what they call a

 

547

00:48:06,160 --> 00:48:11,360

genetic signature, and it's unique to that patient and their cancer. It's about 16 unique, what they

 

548

00:48:11,440 --> 00:48:16,720

call molecular identifiers that they found are not only unique to that patient, but they don't

 

549

00:48:16,720 --> 00:48:22,000

change over time. They don't change as a result of treatment. So that's sort of their genetic

 

550

00:48:22,000 --> 00:48:27,440

signature forever for that cancer. And they can get a blood sample from the patient and actually

 

551

00:48:27,440 --> 00:48:33,440

look for that pattern and measure what's known as circulating tumor DNA. And you may see that

 

552

00:48:33,440 --> 00:48:37,600

abbreviated CT DNA, but you can think of that as basically fragments of cancer DNA. So we're able

 

553

00:48:37,600 --> 00:48:42,800

to actually take a blood sample, look not just for cancer cells, but little pieces of cancer DNA

 

554

00:48:42,800 --> 00:48:47,040

from inside cells. And I found that to be really helpful in addition to the other testing we talked

 

555

00:48:47,040 --> 00:48:53,520

about, because if you're negative on Signatera, 0.00, no evidence of cancer, and you show over time

 

556

00:48:54,080 --> 00:48:59,440

that you remain at 0.00, your chance of recurrence is extremely low. So that gives our patients a

 

557

00:48:59,440 --> 00:49:04,080

lot of confidence in only the treatments working and that they're maintaining that no evidence of

 

558

00:49:04,080 --> 00:49:09,040

disease status, but that once they reach a certain point that their chance of that cancer coming

 

559

00:49:09,040 --> 00:49:14,880

back is very low. Signatera was the name of it. And I want to make, because this was so valuable,

 

560

00:49:14,880 --> 00:49:22,160

what you just mentioned, they're looking at the tissue biopsy in the lab. Are they seeing this

 

561

00:49:22,160 --> 00:49:26,800

tissue within 12 hours, 24 hours that it's been taken out? How soon is this? It can be years old.

 

562

00:49:26,800 --> 00:49:31,840

It can be three, four, five years old tissue that's been preserved, because a pathology lab is

 

563

00:49:31,840 --> 00:49:36,560

required to preserve tissue for up to 10 years. So the pathology lab will have it. The pathology

 

564

00:49:36,560 --> 00:49:41,360

lab has it. And so it's just a matter of getting that sent to Signatera. They're in California. So

 

565

00:49:41,360 --> 00:49:48,560

most US-based hospitals can send it, no problem. And then they spend about three weeks or so

 

566

00:49:48,560 --> 00:49:53,280

working on that pattern. And then the blood testing part takes about a week. So the nice thing is,

 

567

00:49:53,280 --> 00:49:58,800

even though that first result takes about a month to come back, subsequent testing only requires a

 

568

00:49:58,800 --> 00:50:02,240

blood sample, and it takes about a week to come back. So it's a really nice way. We use that to

 

569

00:50:02,240 --> 00:50:07,040

monitor our treatments as we go, but then also after treatment to make sure the patient keeps

 

570

00:50:07,040 --> 00:50:12,160

doing well. And you mentioned the zero, zero, zeroes, right, for no evidence of disease.

 

571

00:50:12,800 --> 00:50:19,600

For the period of time that you've been working with this lab, do you feel a level of greater

 

572

00:50:19,600 --> 00:50:26,560

confidence with those results versus an image? Or would you recommend both? I recommend both,

 

573

00:50:26,560 --> 00:50:34,160

but I have found that we can usually extend, for some patients at least, extend the amount of time

 

574

00:50:34,160 --> 00:50:41,920

between scans if Signatera remains good. Because the key thing is, on an image, something needs to

 

575

00:50:41,920 --> 00:50:49,440

be about one millimeters or larger to show up. And a one millimeter lesion is about a million cells.

 

576

00:50:49,440 --> 00:50:54,720

So if you can imagine, that's a lot of cells in order to be detectable on a PET scan or a CT.

 

577

00:50:55,520 --> 00:51:01,360

With Signatera measuring just fragments of cancer cell DNA, it's a much, much smaller entity. So

 

578

00:51:02,080 --> 00:51:06,240

I'm very careful to say we don't need to exclusively rely on Signatera. It's not designed

 

579

00:51:06,240 --> 00:51:11,280

to be a standalone, but to supplement imaging, I think it's a really good strategy. Because we're

 

580

00:51:11,280 --> 00:51:17,840

going to capture a lot if we combine Signatera with imaging with regular lab testing as well.

 

581

00:51:18,800 --> 00:51:25,760

So if you're doing the Signatera, a patient that's already gone through the Center for Advanced

 

582

00:51:25,760 --> 00:51:33,120

Medicine, get a Signatera test every six months, every three months? Good question. So we get a

 

583

00:51:33,120 --> 00:51:39,280

test at baseline, and then we actually will test again after about a month of treatment. So in the

 

584

00:51:39,280 --> 00:51:44,240

context of our 12-week treatment program, about week six when they're home, for those that break

 

585

00:51:44,240 --> 00:51:49,200

in the middle, we'll do another Signatera. And the nice thing is we'll have both the baseline and

 

586

00:51:50,240 --> 00:51:54,560

that roughly six-week Signatera back before they come back for their last four weeks of treatment.

 

587

00:51:54,560 --> 00:51:58,480

So if we need to tweak anything, we can. I mean, we typically see that number come down,

 

588

00:51:58,480 --> 00:52:02,640

meaning the cancer load is less. But if we need to tweak something, we can. And then we'll actually

 

589

00:52:02,640 --> 00:52:07,840

check another one about two weeks after they finish the 12 weeks of treatment. And then beyond that,

 

590

00:52:07,840 --> 00:52:12,640

it really depends on what we see. If the Signatera is positive, meaning it's showing some cancer

 

591

00:52:13,200 --> 00:52:19,040

activity there, then we typically will do it monthly. And if it's negative, meaning 0.00 in

 

592

00:52:19,040 --> 00:52:23,360

abundance of cancer, then we do it every three months. Okay. And then as far as the imaging,

 

593

00:52:23,360 --> 00:52:30,320

let's say a PET CT once every six months, once a year? Yeah, it depends on the patient.

 

594

00:52:31,360 --> 00:52:35,520

Typically we'll get an imaging before we start treatment and then again, about two weeks after

 

595

00:52:35,520 --> 00:52:40,720

we finish. So that'll be a three months in between those because that's measuring treatment. After

 

596

00:52:40,720 --> 00:52:45,040

that, no more often than every three months, but most often I'll wait six months for a lot of

 

597

00:52:45,040 --> 00:52:49,520

patients moving forward. Do the image. Okay. And sometimes a year, it just depends on the patient.

 

598

00:52:50,240 --> 00:52:53,840

And I know this is such an important topic for patients because they're like, they want to make

 

599

00:52:53,840 --> 00:52:58,160

sure that, well, there's no evidence of disease, right? I'm not going to use Orcure or you're

 

600

00:52:58,160 --> 00:53:09,600

cancer-free. However, if the patient wants to do the Signatera test more frequently, because they

 

601

00:53:09,600 --> 00:53:13,280

just want to, they're willing to pay for it. Are you willing to support them? Sure. Okay.

 

602

00:53:13,280 --> 00:53:18,960

Absolutely. And so for how long, maybe we have to go out years. I don't know if this is two years,

 

603

00:53:18,960 --> 00:53:27,200

five years. For how long of a period of a time do they need to see those negative 0.00 to really

 

604

00:53:28,000 --> 00:53:33,280

be in that spot where you think as a professional, as an integrative oncologist, where you're like,

 

605

00:53:34,240 --> 00:53:42,240

you're okay. Yeah. Signatars research has really put a lot of weight on that two-year mark. So two

 

606

00:53:42,240 --> 00:53:51,440

years of consistently negative Signatars results. So 0.00 every three months up to that two-year

 

607

00:53:51,440 --> 00:53:55,200

mark, the risk of recurrence is extremely low in their research. So it's not to say we don't need

 

608

00:53:55,200 --> 00:54:00,240

to still monitor it after that because we do, but I would say we would do it less frequently,

 

609

00:54:00,240 --> 00:54:04,560

maybe go to every six months at that point or every, or just know that even if we are sticking

 

610

00:54:04,560 --> 00:54:08,800

with three months, that the chances of recurrence are low. What I'm hearing you say is you have a

 

611

00:54:08,800 --> 00:54:16,080

very systematic approach when it comes to measuring the response when the patients come to you. This

 

612

00:54:16,080 --> 00:54:24,400

is so important. What about the whole idea that somebody's cancer can be completely resolved in a

 

613

00:54:24,400 --> 00:54:29,600

period of two or four weeks going to some integrative or alternative? I mean, what are the chances? I

 

614

00:54:29,600 --> 00:54:34,160

mean, outside of a true miracle, right? But I'm not talking about a true miracle from God. I'm

 

615

00:54:34,960 --> 00:54:38,880

talking about medicine. I mean, what are the chances of this even happening?

 

616

00:54:38,880 --> 00:54:43,680

Right. Thank you for asking that. Cancer by all estimations takes a long time to develop. I mean,

 

617

00:54:43,680 --> 00:54:49,440

just because someone has identified a tumor, it didn't just pop up right then. It took years

 

618

00:54:49,440 --> 00:54:55,360

to develop. And so the notion that you can get rid of it in just a few weeks is ludicrous. So

 

619

00:54:56,080 --> 00:55:00,240

that's exactly why we have a 12-week program. And it's not a guarantee that your cancer will

 

620

00:55:00,240 --> 00:55:05,440

be gone in 12 weeks. We have had patients that had that even stage four, but I'm not going to

 

621

00:55:05,440 --> 00:55:09,680

promise that people. I mean, you have to just understand that that's a starting point and you

 

622

00:55:09,680 --> 00:55:14,400

may need more treatment than that. And we know that because we monitor patients really closely.

 

623

00:55:14,400 --> 00:55:20,240

And so everyone's different. I haven't treated you. So you may need more than that, but I'm

 

624

00:55:20,240 --> 00:55:23,840

confident you don't need less than that. There's just no way if you've never treated your cancer

 

625

00:55:23,840 --> 00:55:27,600

with any legitimate treatments that you can just get rid of it in three or four weeks. There's no

 

626

00:55:27,600 --> 00:55:33,840

way. This is a long distance marathon for the patient. It is. It is. Because if a patient's

 

627

00:55:33,840 --> 00:55:39,280

coming to us with a tumor, we have a lot of work to do, whether it's a stage one or a stage four.

 

628

00:55:40,560 --> 00:55:46,240

There's a lot going on to get to that point that we need to address. Okay. Fantastic. It's good to

 

629

00:55:46,240 --> 00:55:51,920

know. Very valuable insights that you're giving us here, Dr. Stegall. In your book, Cancer Secrets,

 

630

00:55:51,920 --> 00:55:59,360

there was something I read. You talk about the grim reality when it comes to conventional

 

631

00:55:59,360 --> 00:56:08,560

chemotherapy, that there's no studies being done on fractionated chemo. And let's face it, if there

 

632

00:56:08,560 --> 00:56:15,760

were, and it was found to be more advantageous to do fractionated doses of chemotherapy,

 

633

00:56:15,760 --> 00:56:21,120

the pharmaceutical companies would end up losing a great deal of money in that process. Is that

 

634

00:56:21,120 --> 00:56:27,200

correct? It is. There's really no incentive to pay for those studies, especially since most of

 

635

00:56:27,200 --> 00:56:32,720

these chemo drugs are off patent. A lot of them are, so they're generic on some level. And so

 

636

00:56:34,560 --> 00:56:39,200

the money's going into new drugs. They can be patented. They can be, they can cost a whole

 

637

00:56:39,200 --> 00:56:43,280

bunch of money that someone has to pay for, typically insurance companies. So yeah, there's

 

638

00:56:43,280 --> 00:56:49,280

really no financial incentive to do research on lower doses of chemo. However, since I wrote my

 

639

00:56:49,280 --> 00:56:53,520

book, and actually I want to mention the second edition of Cancer Secrets is coming out here in

 

640

00:56:53,520 --> 00:56:58,400

the next couple of weeks. But one of the things I updated in there is some new research on

 

641

00:56:59,280 --> 00:57:05,760

low dose chemotherapy versus full dose. And it's really fascinating, a group, again, it wasn't a

 

642

00:57:05,760 --> 00:57:10,800

drug company that did this study. It was just a group of just cancer doctors that decided we

 

643

00:57:10,800 --> 00:57:16,160

wanted to study lower doses of chemo. So they looked at advanced cancers, or they looked at

 

644

00:57:17,120 --> 00:57:26,160

stage four lung cancer, stage four colon cancer, stage four ovarian cancer, and any stage pancreatic

 

645

00:57:26,160 --> 00:57:30,880

cancer. So these are all advanced aggressive cancers, right? They took, they put these patients

 

646

00:57:30,880 --> 00:57:35,200

into two pretty much identical groups and made sure that the patients were very similar in terms

 

647

00:57:35,200 --> 00:57:42,640

of their average age, gender, extent of cancer, all that. So they gave one group full dose chemo.

 

648

00:57:42,640 --> 00:57:49,280

They gave another group low dose chemo, which they defined as 50% or less of the full dose.

 

649

00:57:50,000 --> 00:57:54,160

And they not only followed these patients for a few weeks or a few months, they followed them for

 

650

00:57:54,160 --> 00:58:00,480

10 years. And what they found is, first of all, no one in the full dose chemo group lived 10 years.

 

651

00:58:01,200 --> 00:58:05,840

And only one person in the full dose chemo group lived five years, but they had multiple people in

 

652

00:58:05,840 --> 00:58:12,480

the low dose chemo group that lived 10 years. And so they found that the average survival was higher

 

653

00:58:12,640 --> 00:58:17,600

for all cancer types with full dose, I mean with low dose chemo compared to full dose. So the low

 

654

00:58:17,600 --> 00:58:23,920

dose chemo patients live longer than the full dose did, significantly so with some of the cancer

 

655

00:58:23,920 --> 00:58:28,160

types they looked at. And as you would expect, the side effects risk was lower as well,

 

656

00:58:28,160 --> 00:58:33,440

the side effects. So they live longer and they had fewer side effects. That sounds like a great deal,

 

657

00:58:33,440 --> 00:58:40,000

doesn't it? Yes, absolutely. So my hope is that with this research, which has not been published,

 

658

00:58:40,000 --> 00:58:43,760

but it has been released. So I don't know if it's been published as of now, it had not been a couple

 

659

00:58:43,760 --> 00:58:51,040

weeks ago. But it's legitimate research, it's out there. And I'm excited about it because this

 

660

00:58:51,040 --> 00:58:57,360

hopefully will encourage others to do similar research, right? We need this. Absolutely. And

 

661

00:58:57,360 --> 00:59:01,280

I'm excited because I see this in my practice all the time. I mean, I see it all the time.

 

662

00:59:02,320 --> 00:59:08,000

But everyone says, well, where's the data? Where's the data? Well, here's some data. So it's very

 

663

00:59:08,000 --> 00:59:13,520

exciting and it reinforces everything I believe to be true. This is very interesting because

 

664

00:59:14,800 --> 00:59:18,640

obviously the pharmaceutical companies are not going to fund these studies, but this was a group

 

665

00:59:18,640 --> 00:59:23,680

of doctors that did this on their own. And this is really what it appears it's going to take in the

 

666

00:59:23,680 --> 00:59:28,480

future. Doctors like yourself, they're really willing to put their money where their mouth is,

 

667

00:59:28,480 --> 00:59:33,280

where they will make the financial investment to find out, hey, is this integrative stuff working?

 

668

00:59:33,280 --> 00:59:38,640

Is this different way? This other way of doing this, will it work? So this is exciting. And

 

669

00:59:39,920 --> 00:59:43,760

you're talking about this in your next book that's coming out. Yes. The second edition of Cancer

 

670

00:59:43,760 --> 00:59:47,600

Secrets, which will be out in the next few weeks, that's in there as well. What's the title of the

 

671

00:59:47,600 --> 00:59:52,880

next book? Cancer Secrets, second edition. Okay. So it's the same title everyone is familiar with.

 

672

00:59:54,080 --> 01:00:00,080

And just to remind everyone, that was with low dose chemo. That didn't even include IPT. That

 

673

01:00:00,080 --> 01:00:04,320

didn't include fasting. That didn't include getting your diet right. It didn't include taking

 

674

01:00:04,320 --> 01:00:07,280

the right supplements. It didn't include all these other things that I think are also very

 

675

01:00:07,280 --> 01:00:12,480

relevant. That was simply looking at chemo full dose versus a lower dose. Wow. So yeah.

 

676

01:00:12,480 --> 01:00:18,960

That's super encouraging because we know that all these other tools that you're going to use

 

677

01:00:19,840 --> 01:00:27,920

are going to help the patient. That is fantastic. Now, give us the name of your website where people

 

678

01:00:27,920 --> 01:00:33,520

can go to your podcast and get all kinds of frequently asked questions answered. Sure. So

 

679

01:00:33,520 --> 01:00:38,320

the best place to go is cancersecrets.com. You can find information about my podcast. You can listen

 

680

01:00:38,320 --> 01:00:46,720

to all the previous episodes on there as information about my book. And then also I recently released a

 

681

01:00:46,720 --> 01:00:50,960

cancer course, an online course that they can find out about on that site as well. It's called Cancer

 

682

01:00:50,960 --> 01:00:57,280

Secrets University, but it's basically a lot of video modules of me teaching on various topics.

 

683

01:00:57,280 --> 01:01:01,920

What is cancer? How do you get cancer? Going through all the different therapies, conventional

 

684

01:01:01,920 --> 01:01:06,320

and natural therapies. What the research is on these. What I recommend to my patients in my

 

685

01:01:06,320 --> 01:01:11,040

practice. So I think that's something people will really benefit from. That's fantastic. That is

 

686

01:01:11,040 --> 01:01:16,560

absolutely fantastic. So exciting, Dr. Stegall. Well, listen, everyone, I hope you notice that

 

687

01:01:16,560 --> 01:01:22,640

Dr. Jonathan Stegall is one of the leading up and coming integrative oncologists in the United States.

 

688

01:01:23,440 --> 01:01:27,520

He's not afraid to tackle a subject. He's not afraid to answer the difficult questions.

 

689

01:01:28,080 --> 01:01:34,080

And I could spend another three hours with him in this room, but unfortunately, Dr. Stegall has

 

690

01:01:34,080 --> 01:01:41,840

patients that he's committed to. But I highly recommend that you go to his website, tcfam.com.

 

691

01:01:41,840 --> 01:01:50,400

Once again, that's the letter T-C-F-A-M.com and find out about getting a consultation with

 

692

01:01:50,400 --> 01:01:55,280

Dr. Stegall. It's not going to be an eight minute consultation. It's going to be an hour or 90

 

693

01:01:55,280 --> 01:01:59,840

minutes or who knows how long it's going to be, but you're going to receive the personal touch

 

694

01:01:59,840 --> 01:02:05,280

that you deserve when it comes to a cancer diagnosis. Dr. Stegall, I want to thank you

 

695

01:02:05,280 --> 01:02:08,320

for coming in here today. Thank you. I really appreciate it. I appreciate it.

 

696

01:02:08,320 --> 01:02:11,600

All right. I'll do this again soon. Yes. Keep up the good work. All right. Thank you.

 

697

01:02:11,600 --> 01:02:13,680

All right. God bless you. God bless you.