September 24, 2005

The Crawford Resignation Mystery

True to form, the administration picked late Friday afternoon to announce that Food and Drug Administration commissioner Lester Crawford resigned. The veterinarian in charge of the world's premier food and drug safety agency, who was confirmed for the job just two-and-a-half months ago, cited his age. He is 67.

The Saturday morning papers (the least read of the week; that's why troubling announcements get released late Friday) gave no clues as to what drove the decision, although both the New York Times and the Washington Post hinted broadly that he was forced out. But why? It couldn't have been the postponement -- again -- of approving Plan B, the morning after contraceptive pill. Crawford was doing the administration's bidding on that issue.

One possible clue to the administration's thinking comes from the appointment of Andrew von Eschenbach, head of the National Cancer Institute, as acting commissioner. Von Eschenbach, who previously ran the M.D. Anderson Cancer Center at the University of Texas, has been touting the new generation of targeted cancer drugs and in recent speeches has been confidently predicting that cancer would become a manageable disease -- like AIDS -- by 2015.

The Post story mentions that many oncologists have criticized von Eschenbach for overpromising, but ignores the back story. His prediction and embrace of the latest drugs has been prominently featured by the conservative Manhattan Institute, whose work on FDA and medical issues is conducted at its Center for Medical Progress. The Center is funded by the drug industry.

In the world of journalism, the Wall Street Journal's editorial page has been touting the new cancer therapies even when the clinical trial evidence shows they don't work or help as few as 10 percent of patients (and even then only for a few months). The Journal has been on the warpath against Richard Pazdur, who runs the FDA's oncology bureau, claiming he has slowed the pace of drug approvals.

Paul Goldberg's influential "Cancer Letter" pointed out in its August issue how a right wing "insurgency" is pushing for early approvals of cancer drugs. The insurgency includes Michael Milken (who has been treated for prostate cancer) and an all-star cast of conservative think tanks like the Manhattan Institute, the American Enterprise Institute, the Cato Institute, the Competitive Enterprise Institute, the Washington Legal Foundation and a cancer patient advocacy group known as the Abigail Alliance.

Grabbing a page from the AIDS activists of the early 1990s, their slogan is early access to experimental cancer drugs for the dying. If they can get the FDA to approve early access based on experimental data that suggests a new, experimental drug may affect the disease (usually based on some surrogate marker like tumor shrinkage, which can have no relationship to survival), they can then force insurance companies, Medicare and Medicaid to pay for the treatments.

That would be a godsend to the drug industry, which has invested billions in searching out cancer cures with marginal success. The new targeted therapies can cost anywhere from $4,000 to $10,000 a month. No wonder it has financially supported many of the conservative groups in the coalition.

Pazdur, who also came to the FDA from the M.D. Anderson Cancer Center, has fought to hold the line for the agency's traditional standard that a drug be shown to be effective before getting approved. His staff has also done a good job assessing whether a new drug's usually marginal benefits outweigh the substantial side effects and risks that are often associated with cancer therapies, including the newer targeted therapies. Just yesterday Genentech announced it had to stop a trial of its new drug Avastin for ovarian cancer after 11 percent of patients began developing holes in their stomachs and intestines.

There is a serious discussion that needs to take place at the FDA about how companies with new therapies can be encouraged to collaborate to see if in combination these drugs can have a major impact on cancer. But sophisticated scientific discussions and breaking the entrenched habits of competitive drug firms is not what the ideologues behind the anti-Pazdur campaign have in mind.

If von Eschenbach forces his former colleague out and appoint someone more malleable to run the agency's oncology division, we'll know the real reason why Crawford resigned.

Posted by gooznews at September 24, 2005 10:42 AM
Comments

If was just to ease out Crawford to make room for Von Eschenbach, they would have told him to step aside and retire gracefully. This 345 pm resignation does not seem consistent iwth the way they would treat a good soldier who took his orders well. Obviously, they had cleared this with Von Eschenbach ahead of time, but it happened very quickly, methinks. Crawford could have done a Linda Skleadny and just gone quickly and quietly "to spendmore time with family."

Yes, you are right, there are those who would like to see drugs simply released to the public. Naming Scott Gottlieb to be advisor for science for Crawford at a time when concern for drug safety is high and his thing is to release drugs earlier...by the way, Gottlieb used to write those ridiculous WSJ editorials on FDA killing people by taking time to review applications and may still have sway there....

I am tempted to take WH rumors at face value...that there are continuing problems with Crawford's background and disclosure...and that they needed to dump him before press caught wind...but they couldn't just fire him because it would put Janet Woodcock in position to take over. They did need to find someone else.

Posted by: John at September 25, 2005 09:00 AM

I think it's wonderful that Scott Gottlieb, and Dr Von Eschenbach, have chosen public service at the FDA. Despite his youth, Dr. Gottlieb is brilliant; he has a medical degree and years of prior service at the FDA under Dr. McClellan. He has been a critic of the FDA (criticism which it deserved) and thank God he is willing to spend time trying to bring timely cures to the American people, when he could be making a lot more money as a private physician or doing just about anything else. As a tax-payer I am pleased to see forward thinking and positive change at the FDA, whose role after all is to bring safe, effective therapies to the American people, and I think President Bush has done an outstanding job in his selection of both fine men to do just that.

Posted by: Jennie at October 4, 2005 04:03 PM