Showing posts with label cancer drugs. Show all posts
Showing posts with label cancer drugs. Show all posts

Nov 7, 2015

Clinical Trials, Big Pharma, the FDA, and Expen$ive Drugs


...turns out this is not always a great combination for patients
 
Many of us, including this author, are taking one or more of the new and very expensive cancer drugs in our attempt to live longer and have a better quality of life. New and expensive does not necessarily mean we will live longer and better, however. We keep doing this (at least I do) because there is not much in the way of alternatives. We seem to be at the mercy of the most powerful companies in the U.S.

In a new book, Ending Medical Reversal: Improving Outcomes and Saving Lives, Dr. Vinay Prasad looks at ever increasing prices, secretive clinical trial results, questionable procedures, and low drug effectiveness in dozens of the new cancer drugs on the market. Dr. Prasad is an Associate Professor of Medicine at OHSU.

Here are some excerpts from Dr. Prasad’s book in his own words:
"Cancer drugs are outrageously expensive; but they are worth every penny, right?
When you pay a lot for something, you want it to be great. This is true of a new car, a new computer, a new pair of shoes—but it doesn’t seem to be true for cancer drugs.
Recently, we heard that profiteers are raising the price of old, established medicines. For many Americans, Turing pharmaceutical and Martin Shkreli have become four letter words.
But the problem of inappropriate prices is not just a few exceptional cases; it is the norm in cancer medicine.
Before we talk price tag, let’s consider what we get for our money. In medicine, there is always nuance, and it exists here. For example, there are some excellent cancer drugs. Two that come to mind are imatinib—a revolutionary pill that transformed a highly fatal leukemia into a manageable condition—and rituximab—a monoclonal antibody that has improved survival in several cancers. These drugs are expensive, sure, but no one can say they aren’t terrific. But we can say that Novartis, the maker of Gleevec, has raised the price of the drug from an already high $30,000 in 2001 to $76,000 today despite the fact that it costs less than $200 dollars to manufacture a year's supply.
But at least Gleevec is a great drug. Most cancer drugs are not close to being great—they have only a tiny positive impact on longevity and often cause many side effects.
The median improvement in survival for 71 drugs approved by the US Food and Drug Administration for treating solid cancers over the last decade is only 2.1 months. And there are two good reasons to assume that this remarkably short reported extension is in fact an overestimate. First, the average age of cancer patients in the real world is much older than those included in the studies submitted to the FDA —60% of cancer patients are over 65, but they account for just 36% of patients in key trials. Older patients—who are frailer and have other medical problems—experience more side effects from cancer drugs and less benefit.
Second, the majority of cancer drugs approved by the FDA are not included in the 2.1 month figure, because their effects on overall survival are unknown. Amazingly, most new drugs (2/3s) are approved on the basis of improvement of a surrogate endpoint—e.g. a new drug shrinks a tumor on a CT scan. We don't know that this shrinkage actually translates into a longer or a better life.
So, the efficacy of most cancer drugs is minimal and may be even less in the real world. How do we then explain why they are already so ridiculously expensive and increasing in cost at a rate of 10% a year. Cancer drugs now routinely cost more than 100,000 dollars for one year of treatment.
One way doctors measure the value of drugs is to ask how much is the total drug cost to get us 1 year of quality life. Since most drugs just add a few weeks or months, you have to treat many people to get just one year of extra life. By this measure, most cancer drugs are outrageously expensive. A new breast cancer drug costs ~$700,000 for a quality adjusted life year, and a new colon cancer drug costs $900,000. And these figures apply only if you give the drug the benefit of the doubt, and assume it works as well in the real world as it does in FDA studies.
Not surprisingly, Pharma is our most profitable industry—double digit returns ranging from 10% to 42% are routine, despite the overall disappointing benefits of their products.
Reasonable people would say it’s fine to make a tidy profit when you make a great drug—a drug like Gleevec. But we might also say it doesn’t seem fair to keep raising its price over time, as the cost to make it is trivial, and the research and development are already done. Steep price increases feel like profiteering.
Reasonable people might also say that it doesn’t seem right to pay so much for drugs that add so little—and only add that little bit under just right conditions. Especially when the costs to make drugs are so low and profits are so high.
What prevents us from being reasonable people? That is not just a million dollar question, but a tens of billion dollar one. It involves rules that prevent Medicare from negotiating the price of drugs and the intricacies of the patent system. Solutions won’t be simple or easy, but the price of cancer drugs is way too high, and we get far too little for it. The time for reform is now."
As someone who is about to embark on yet another expensive cancer drug experience I applaud Dr. Prasad. I wish him well and hope he can convince enough of the right people (maybe even Congress) to take another look and maybe even take action to decrease drug costs. My life, and many of yours, may depend on it.


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To put a smile on your face see Larry's latest cartoon.
To learn more about clinical trials, take a look at our book.

(c) 2012 Tom Beer and Larry Axmaker

Apr 3, 2013

Myths and truths about cancer clinical trials


Myth #1—Cures already exist for many cancers but drug companies are keeping them under wraps in order to make even higher profits when they are released or to profit from current less effective drugs.

Truth #1—You gotta be kidding! The world drug market is large and very competitive and no pharmaceutical company is going to give up a chance to market a great product. Holding back could give other companies a chance to develop and market a similar drug.

Myth #2—Many experimental cancer drugs in the U.S. have already been tested and approved in other countries.

Truth #2—Sometimes drugs ARE available first in other countries. But the U.S. is by far the world leader in cancer research and new drugs are more often than not available to Americans first.

Myth #3—If I join a clinical trial, whether it is successful or not, I’ll be disqualified from ever participating in a trial again.

Truth #3—Nope. Many people with cancer participate in two, three, or more trials in their lifetime. This author (LWA) has participated in three clinical trials and is considering a fourth. Your previous history, including clinical trials, could be considered when you apply for a new clinical trial. Do your homework and make sure joining a trial is in your best interests.

Misconception #4—In almost all cases, drug testing can be done in test-tubes, with animals, and by computer simulations. Testing on humans is seldom necessary.

Answer #4—Don’t we all wish! It would certainly be faster and cheaper if people were not needed in the drug approval process. But, in fact, testing on humans is currently the only way to determine proper dosages, the effects of side effects, and whether or not the drug actually cures or manages cancer.

Myth #5—Drug companies pay hospitals and doctors a lot of money to ensure they get the best possible results from clinical trials. The better the results, the higher the payments.

Truth #5—The pharmaceutical companies often pay for some or most of the costs of a clinical trial. These payments are never linked to the results of the trial.  And, at the end of the day, academic centers do not make a profit on clinical research.  There are several layers of safeguards to make sure trials are conducted scientifically and accurately.

Myth #6—Most clinical trials only accept participants who have the least serious and dangerous types of the cancer being tested in the trial in order to improve the chances of getting good results.

Truth #6—Cancer treatment drugs are developed for all levels and stages of cancer. Some trials, however, may exclude patients with serious heart, lung, kidney, or liver diseases to protect them from unknown side effects. After a drug is proven successful and safe, these high-risk people may be included in further studies.


To put a smile on your face see Larry's latest cartoon.
To learn more about clinical trials, take a look at our book.

(c) 2012 Tom Beer and Larry Axmaker

Feb 23, 2013

What process does the FDA follow when determining whether to approve a drug?


FDA approval doesn’t actually take as long as most people think.  In a recent blog post, http://www.cancer-clinical-trials.com/2012/07/waiting-for-new-drug-to-be-approved.html we discussed the fact that FDA approval, at an average of 322 days, is actually a little faster than approval in Europe and Canada.  That’s not to say it’s quick, but it does not take years.  What takes a long time are all the studies necessary to collect the information the FDA requires to consider an application.  The FDA uses the “safe and effective” standard.  Effective means that cancer patients benefit in a meaningful way.  This often involves living longer, being cured of cancer, or experiencing quality of life improvements.  The FDA reviews all of the clinical trial data in detail to determine if these standards have been met.  This review takes several months.  While we all want cancer drugs to come to market as quickly as possible, it is also worth remembering that the FDA is held accountable when a drug is approved that later proves unsafe.  It’s a balancing act between moving quickly and dotting the i’s and crossing the t’s.

For more questions and answers about clinical trials, visit the Talk about Health website.
To put a smile on your face see Larry's latest cartoon.
To learn more about clinical trials, take a look at our book.

(c) 2012 Tom Beer and Larry Axmaker

Jan 21, 2013

How does the FDA know about new side effects for a drug that has already been approved?


The FDA has surveillance programs in place to monitor the safety of drugs after approval.  These programs primarily rely on physicians reporting to the FDA the side effects they see.  While not all physicians routinely make such reports, enough do that unexpected side effects usually come to light.  For some drugs that are approved with some questions about safety, special requirements can be put into place.  These might include so called phase IV studies to gather more safety data or special prescribing programs for high-risk drugs.

For more questions and answers about clinical trials, visit the Talk about Health website.
To put a smile on your face see Larry's latest cartoon.
To learn more about clinical trials, take a look at our book.

(c) 2012 Tom Beer and Larry Axmaker

Dec 19, 2012

What metrics are typically used to determine if the drug is successful?


The ultimate success of a new drug or drug combination is judged by the “safe and effective” standard.  Both of course are examined in context.  Safe often means safe enough – or no less safe than what we have today.  Some cancer treatment have severe side effects – but because their benefits are judged acceptable – they are approved.  Effective means that cancer patients benefit in a meaningful way.  This often involves living longer.  When survival is not impacted, meaningful quality of life improvements are required.  In some situations, cure rates are the measure of success.  Survival benefit, which is the most common measure of success, can take a year to several years to determine.

For more questions and answers about clinical trials, visit the Talk about Health website.
To put a smile on your face see Larry's latest cartoon.
To learn more about clinical trials, take a look at our book.

(c) 2012 Tom Beer and Larry Axmaker

Aug 19, 2012

Some Clinical Trials Can’t Recruit Enough Participants

Does that surprise you? In fact, participation in cancer clinical trials is very low. The National Cancer Institute (NCI) reports that only about 3 percent of all adult cancer patients ever participate in a clinical trial. And the participation rate of seniors (who have about 2/3 of all diagnosed cancer cases) and ethnic minorities is much lower—only about 1 percent!

Clinical Trials are the process by which new cancer drugs and treatments are tested and finally approved for use by the U.S.Food and Drug Administration.

What happens if there aren’t enough volunteer participants for a clinical trial to be conducted? In that case we will not find out if the untested drug might actually have benefitted those with cancer. This happens frequently.

Why don’t cancer patients participate in clinical trials?
The NCI reports multiple reasons:

·       Lack of awareness—one survey found that 85 percent of cancer patients were not even aware that they might qualify for a clinical trial.
·       Some cancer patients have a distrust of research and those who conduct trials.
·       There is reluctance by some physicians to refer patients to trials.
·       Travel to trial centers and the time required to participate in a trial is cited by some patients.
·       Cost factors—travel to clinic sites and additional medical costs can be deciding factors.

·       On the plus side, a survey of people who had already participated in a cancer clinical trial found that 84 percent said they would participate in another trial if given the chance. And most states now require health insurance providers to cover the ‘routine’ costs of a trial.

May 25, 2012

Cancer Drug Side effects: Are you getting the whole story?


In a word (or two), maybe yes and maybe no.  Lists of side effects are easy to find.  Every drug has them.  These lists may be so long that they become almost meaningless.  As you leaf through these listing, several questions arise: 
1)    Is the list complete? Are there any side effects missing that I need to know about?
2)    Are all these side effects really caused by the drug?
3)    How do I know which of these side effects may happen to me?

How are side effect reported
We will tackle the first two questions, the third deserves its own blog post.  Researchers who study new cancer drugs are the first to report side effects.  Side effects can also be reported to the FDA after a drug is approved and regularly prescribed. Researchers report every adverse event that happens to their patients who are participating in a clinical trial.  Adverse events are reported together with their grade and “relationship to treatment.”  The grade is a measure of severity and for every imaginable adverse event, there is a table that describes what is mild (grade 1), moderate (grade 2), severe (grade 3), and life threatening (grade 4).  Clinic notes in research centers are filled with these mysterious grades whenever anything untoward happens. 

The relationship to treatment is determined by the research physician’s best judgment about whether the adverse event was caused by the drug or not.  There are shades of grey here:  related, probably, possibly, unlikely, and not related.  The decision is basically a judgment call, an educated guess.  Sometimes it’s obvious: you are feeling great and get the flu along with your entire family.  Pretty unlikely the drug had anything to do with it.  Often it is not so obvious.  People with cancer may also have other medical conditions and take many different drugs.  The illness itself takes a toll. When something untoward happens, there are many possible causes. 

With all this reporting, how could side effects go unnoticed?
Rare side effects can, of course, go unnoticed if they didn’t happen during the study.  Sometimes, the source you are relying on (i.e. research paper) listed only a subset of the

May 20, 2012

Answers to questions you always wanted ask - an interview with Dr. Barken

Dr. Israel Barken runs a wonderful site called Ask Dr. Barken.  He was kind enough to interview Dr. Beer about clinical trials.  This was an interview that asked the questions you would want to ask.  Unlike some of our other videos...this one is not packed with technical terms and "medicalese" language.  We hope you enjoy this interview.  The original is available on Dr. Barken's site.




To put a smile on your face see Larry's latest cartoon.

To learn more about clinical trials, take a look at our book.
(c) 2012 Tom Beer and Larry Axmaker

Feb 15, 2012

Tom and Larry interviewed on the radio! Listen on Saturday the 18th


Larry and I got a chance to sit down with a radio reporter for an extended conversation about cancer clinical trials.  I biked in the rain to the studio while Larry called in from his sunny patio in the southern Arizona desert.  You can tell right away who is the smarter partner in this writing partnership!

If you would like to listen in, you have two options.  In the Portland metro area, you can tune in to KXL 101 FM.  If you are anywhere else in the world, the show will be streamed live online at  http://www.kxl.com/pages/main.

The show airs at 8 AM Pacific Time (11 AM Eastern Time) on Saturday, February 18th.  


UPDATE:  If you missed the show and would like to listen, click here.


To put a smile on your face see Larry's latest cartoon


(c) 2012 Tom Beer and Larry Axmaker