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We might for the first time really be thinking of cures of cancer’

KocoPr profile image
32 Replies

michiganmedicine.org/health...

When Max Wicha, M.D., was starting his career, oncology did not come highly recommended.

"When I first got into this field about 40 years ago, I went for advice to someone who was very senior in medicine. I said I want to go into cancer research and become an oncologist. They looked at me and said, 'Why would you want to waste your life on that? We're not going to make progress against cancer. It's the least scientific of any discipline. Go into some other field where you can really use science,'" Wicha recalled.

"Of course, that turned out to be completely wrong."

In fact, Wicha, the Madeline and Sidney Forbes Professor of Oncology and founding director of the Rogel Cancer Center, jumped into the discipline just as it was taking off. He reflects on the evolution of the field, in this interview, originally published in the Rogel Cancer Center’s Illuminate magazine.

When you were getting started, were you surprised by your mentor's criticism of the field?

Wicha: What they said in a sense was true. Forty years ago, there was a tremendous disconnect between research to understand the biology of cancer and the clinical practice of oncology. The clinical care had very little to do with the science that was brewing in the laboratory.

Initially, when chemotherapy was developed, medical oncologists thought if we find the right combination of chemotherapy, we can cure most patients with cancer. That turned out to be naïve, and there was a lot of discouragement among clinicians when their clinical trials didn’t improve outcomes.

At the same time, basic scientists were coming up with dramatic results in the laboratory, with the first discoveries of oncogenes and tumor suppressor genes.

The basic scientists were saying, “Look, we're starting to understand what cancer is.” But if you went to the clinic, you didn’t see any impact. That was the dichotomy of the field.

How did the National Cancer Act, which was signed in 1971, and the beginning of nationally designated cancer centers start to change this?

Wicha: To make a fundamental impact, we knew we had to take the basic research and figure out how it leads to improvements for patients — not just make discoveries in the laboratory.

Cancer centers became a lot of the engine for cancer research and cancer discovery, which propelled us into the dramatic impact we see now. It’s because of this marriage of basic research, clinical research and what we now call translational research.

When you were tasked with creating a cancer center at the University of Michigan, how did this landscape influence your approach?

Wicha: The challenge was how to get these groups to merge and talk to each other. On the clinical side, we had people in each discipline treating patients in different ways. Not only did they not talk to the basic laboratory scientists, but even more challenging, they didn't talk to each other.

In my own field of breast cancer, a woman then would have to visit multiple specialists, sometimes getting contradictory opinions. It could take more than a month. Patients would say, “Why don't you put your heads together.” Of course, that was the right advice.

When we started organizing our cancer center, which opened in 1986, we decided to experiment with a multidisciplinary breast clinic. We organized either the first or second multidisciplinary clinic in the country. It was a success right from the beginning. Now of course everyone does it.

Then when we started organizing a cancer center, I thought the way to do this was around multidisciplinary programs for each type of cancer. It allowed us for the first time to bring together active teams of people from different disciplines who work on a particular cancer.

It enabled us to start introducing basic scientists to clinicians and move to a more scientific approach to treat patients.

The basic scientists were saying, 'Look, we're starting to understand what cancer is.' But if you went to the clinic, you didn’t see any impact. That was the dichotomy of the field."

--Max Wicha, M.D.

Where are we now in the progress against cancer?

Wicha: It's completely flipped around. Right now, cancer is the most scientific discipline. It's the best example of basic research discoveries changing clinical care.

Melanoma is a good example. First, we developed molecular targeted therapies based on specific mutations in the tumor. But even more successful has been the use of immune stimulators. Here's a disease that was completely fatal. Now, about 60% of patients see a very significant benefit from immunotherapy. Even more exciting, for a percentage of patients, the melanoma isn't coming back. We might for the first time really be thinking of cures of cancer.

In my field of breast cancer, we’ve developed so many different treatments that often we can turn metastatic cancers into chronic diseases. I have patients who have had metastatic breast cancer for over 20 years.

The trick now is to understand what’s different about the exceptional responders and get more patients into that realm. And the real challenge is going to be how to apply this to tumors where we haven't made much progress, like pancreas cancer and brain tumors.

I will almost guarantee you that progress in those areas won't be by accident but by studying the basic biology of those cancers and then applying new ideas based on that.

Are you glad you decided to go into oncology after all?

Wicha: Personally, it's been such a privilege, and I've been so fortunate to have been in oncology during this phase when it went from a primitive discipline to being a scientific discipline making huge advances.

.

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KocoPr
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pd63 profile image
pd63

The fight to beat cancer is a war of attrition, I believe there's no magic bullet around the corner.Not trying to piss on anyone's fries but that's the way I see it.

mrscruffy profile image
mrscruffy in reply topd63

I agree with you, so many types and most will need their own cure. I do believe cures will be born out of genetic manipulation

KocoPr profile image
KocoPr in reply topd63

I get ya! We have heard this for a long time but the article was positive in the respect that this very experienced doctor who realized researchers and clinicians did not communicate at all and so he started up a center of excellence where they pair up researchers and clinicians for each individual cancers and are getting great results.

TC007 profile image
TC007 in reply toKocoPr

As a novice the day I stated research on Pca my first impression was that there is so much scattered data available on different research. Why don't these researchres collaborate ? This requires an integrated approach with both modern and traditional medicines.

KocoPr profile image
KocoPr in reply toTC007

It is still scattered throughout the world but thanks to the internet and now AI the dots will be connected

TJGuy profile image
TJGuy in reply topd63

You need to understand what is happening around the word right now, the whole medical world is beginning to be flipped into gene therapy, medicine will look nothing like it does today in a very short timeframe.

Cancer is 100 some say 200 or more cancers depending how you look at it, actually a new form of PC cancer was just discovered within the last year or so.

But ways to manage these cancers and outright cures are now very possible with new tools recently developed and still being discovered hourly and daily. The whole world of thinking about cancer is about to be flipped on its head.

These new treatments are just around the corner.

anonymoose2 profile image
anonymoose2

We can only hope. Must have incentives for people to devote their whole lives to it.

Monetary is key keeping people interested.

100’s of billions if not trillions to find the cure.

Most of our debt in the US is from Wars. The war on cancer should be in the mix of that debt. But it isn’t.

National Debt USA
TJGuy profile image
TJGuy in reply toanonymoose2

Debt is the result of far more than spending on wars. US budget surpluses were the result of responsible taxation in the later 90s. Irresponsible tax cuts have led to ever increasing total US debt. This never needed to happen These have been political decisions not responsible decisions that lead to debt.

anonymoose2 profile image
anonymoose2 in reply toTJGuy

when I see 60 billion given to Ukraine and another 20 billion to Israel and 4.7 trillion to the Middle East in the last 20 years, my point was directing money for wars and not cancer is pathetic. Yes I agree we should stop spending and our tax rate should be at 87% for everyone. But you know and I know that won’t ever happen.

I bet you in the next 15 years we will have spent another 4 Trillion on wars and less than 3% on cancer research. Point taken?

Ramp7 profile image
Ramp7

For the first 15 years I believed in the magic bullet. My approach now, is to manage it. Just tip the scales in my favor a little

KocoPr profile image
KocoPr in reply toRamp7

I agree! A cure is still >10 years away. I just seems skeptical sometimes because i have heard and read so many recent discoveries but when i search on NIH i see we have known about this pathway/small molecule/tumor marker/suppresor etc for decades. It’s like big oil knowing about climate change for 30 years. Just to much HUGE money in keeping the status quo’s.

turkeyjoe1 profile image
turkeyjoe1

My dad's doctor's said the same sort of things over 40 years ago. It killed him still and my brother 2 months ago. Is it improving? Yes, but very slowly. Follow the money.

Maxone73 profile image
Maxone73

I do not know. I can tell you one thing, Moore's law applied to information still stands.

The abundance of computational power made AI explode (AI existed since the 50es in its first forms). And quantum computing will be the next big jump forward. A few years ago would have been impossible to think that an AI could have devised a drug on its own, taking few weeks instead of few years, forecasting the side effects and going from the lab to the market. Nowadays a bunch of students with a good idea create a startup and start contributing to research in an active way...and there are thousands of such startups. What we call "big pharma" has 1/100th of the power it held even only 20 years ago, when they were the only ones with enough money to create something interesting (they also have less power in controlling the leaks in their information, hence they must be more careful with their behaviour). Public and private research compete with each other in an unprecedented way, pushing research to the limit.

This said, we should start signing petitions for "guinea pigs rights" that would allow us to get non standard treatments as long as they have at least passed phase 1 (example: pluvicto as first line treatment instead of last resort). And we need to push for that cancer name changes I have talked about, to have parallel instead of sequential trials (example: a trial on ALL BRCA cancers, instead of having first to do it on prostate, then on breast...now we know that genomics is the first factor, it's not 1970!), this would speed up research as well.

MoonRocket profile image
MoonRocket in reply toMaxone73

I believe the guinea pig right exists in the US. It's called the Right To Try Law. I think Donald Trump signed this legislation. Oh My!!!!

Here a link to the fact sheet google.com/search?q=right+t...

Maxone73 profile image
Maxone73 in reply toMoonRocket

I trust you 😀

MoonRocket profile image
MoonRocket in reply toMaxone73

Apparently, like all things in life, there are negatives of being a guinea pig, so the good Samaritans of the world are working on improvements. We'll see what comes of it.

KocoPr profile image
KocoPr in reply toMoonRocket

seems very restrictive and you have to have gone through gauntlet of exhausting all approved treatments AND are ineligible to participate in clinical trials.

In other words pretty much on hospice. That is rediculous.

fda.gov/patients/learn-abou...

The Right to Try Act is one way for patients who have been diagnosed with life-threatening diseases or conditions who have tried all approved treatment options and who are unable to participate in a clinical trial to access certain investigational treatment options. FDA’s role in implementing the Right to Try Act is limited to receiving and posting certain information submitted to the agency.

For patients with serious or immediately life-threatening diseases or conditions, the FDA remains committed to enhancing access to promising investigational medicines for those unable to access investigational medical products through clinical trials. This is the mission of our expanded access program. The agency is dedicated to these purposes, and it has been for more than three decades.

The Right to Try Act permits/allows eligible patients to have access to eligible investigational drugs.

A patient who is eligible for Right to Try is a patient who has:

Been diagnosed with a life-threatening disease or condition

Exhausted approved treatment options and is unable to participate in a clinical trial involving the eligible investigational drug (this must be certified by a physician who is in good standing with their licensing organization or board and who will not be compensated directly by the manufacturer for certifying)

Provided, or their legally authorized representative has provided, written informed consent regarding the eligible investigational drug to the treating physician

An eligible investigational drug is an investigational drug:

For which a Phase 1 clinical trial has been completed

That has not been approved or licensed by the FDA for any use

For which an application has been filed with the FDA or is under investigation in a clinical trial that is intended to form the primary basis of a claim of effectiveness in support of FDA approval and is the subject of an active investigational new drug application submitted to the FDA

Whose active development or production is ongoing, and that has not been discontinued by the manufacturer or placed on clinical hold by the FDA

MoonRocket profile image
MoonRocket in reply toKocoPr

When else would you be giving untested meds? You have to at least establish toxicity.

KocoPr profile image
KocoPr in reply toMoonRocket

Oh it’s not the phase of the trial. I agree we have know the toxicity. What I see is it is offered to us at end of life treatment. Why do we have to wait? Why can’t we get the treatment lets say when we first become castrate resistant before chemo or when we first get diagnosed with a Gleason 8 or 9?

MoonRocket profile image
MoonRocket in reply toKocoPr

Drugs, unless already approved, are not manufactured for broad use. As I understand it, there are companies that are responsible for packaging the trial meds for clinical trials.I work for 3 years at a pharma manufacturing facility, it not a simple effort to switch production from one product to another. Product is usually made in batches and packaged in batches. These smaller specialty manufacturers are not setup for the use to the general patient.

TJGuy profile image
TJGuy in reply toMoonRocket

But nothing practical has come of it as big pharma has to agree to the right to try and they just don't allow it for the most part

Maxone73 profile image
Maxone73 in reply toTJGuy

I am not sure. I don't see why big pharma should oppose testing their drugs on patients at different stages when they would have no ethical responsibility about the outcome? The earlier they can use a drug, the more money they make as their user base would be bigger. This is my common sense of course, I don't know which other implications I am not seeing.

MoonRocket profile image
MoonRocket in reply toTJGuy

How do you know this?

TJGuy profile image
TJGuy in reply toMoonRocket

Just what I've read over the past few years, I try to be aware of everything that's going on, read, read, read. I'd love to be shown that things are changing. We need to get that access.

MoonRocket profile image
MoonRocket in reply toTJGuy

TBH, I hope I never need that access.

KocoPr profile image
KocoPr in reply toMaxone73

Extremely good points! Competition will drive inovation! I am always so thankful we in this age have computers and internet so we can as a human species can collaborate and inovate. I remember before computers how hard it was to communicate with anyone and how hard it was to get more than a trickle of scientific news. I would drool with anticipation every month when popular mechanics, astronomy magazines would come out. It is just unbelievable and amazing now!

j-o-h-n profile image
j-o-h-n

One day the answer to eliminating cancer will be found in a Chinese fortune cookie.

Good Luck, Good Health and Good Humor.

j-o-h-n

TJGuy profile image
TJGuy in reply toj-o-h-n

Oh! I hope it wasn't in the one I ate whole without checking for a message.

j-o-h-n profile image
j-o-h-n in reply toTJGuy

Whole........Who knows? In whole maybe out hole whole.

Good Luck, Good Health and Good Humor.

j-o-h-n

Mgtd profile image
Mgtd in reply toj-o-h-n

Have you ever considered publishing your comments?

j-o-h-n profile image
j-o-h-n in reply toMgtd

Yep..... in Mad Magazine.........I was rejected.... But hey "What, me worry?"

Good Luck, Good Health and Good Humor.

j-o-h-n

traxcavator profile image
traxcavator

There are state Right to Try laws.

There is a New Hampshire bill (HB1300) that would make Right to Try available to anyone whose condition is deemed to be incurable. That would include anyone with prostate cancer who is not a candidate for surgery (which is the only existing curative treatment).

If passed, it will also decouple treatment from FDA approved treatments and treatments in the FDA pipeline. This would allow treatments that have passed into the public domain, and treatments that aren't ever going to make enough money to justify an FDA trial.

It also increases the standard for informed consent to avoid any possibility of coercion of patients by medical professionals.

It's somewhat ironic that this bill is at the same stage in the legislative process as an assisted suicide bill. If the latter passes, but not the Right to Try, it will be easier to check out than to get a potentially curative treatment.

John

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