
New Debate Over Vytorin and Cancer
摘要:2, 2008 -- Although two new trials failed to show a cancer link for Vytorin, the cholesterol-lowering drug isn‘t ready to be completelycleared, says the editor of The New England Journal of Medicine。 The worrisome cancer data come from a clinical trial called SEAS, reportedtoday at a major E......
Sept. 2, 2008 -- Although two new trials failed to show a cancer link for Vytorin, the cholesterol-lowering drug isn't ready to be completely cleared, says the editor of The New England Journal of Medicine.
The worrisome cancer data come from a clinical trial called SEAS, reported today at a major European cardiology conference and simultaneously published online by The New England Journal of Medicine. But these findings come as no surprise.
That's because of a highly unusual news conference held last July. SEAS study leader Terje Pedersen, MD, PhD, announced the unexpected finding of a possible Vytorin cancer link. Then he turned the podium over to Oxford University's Richard Peto, FRS, who said his independent analysis of two ongoing Vytorin studies revealed no credible evidence linking Vytorin to cancer risk.
Not so fast, says an editorial by Jeffrey M. Drazen, MD, editor-in-chief of The New England Journal of Medicine, and colleagues. The editorial says we simply can't assume -- as Peto asserts -- that the Vytorin cancer link is simply a chance finding.
"What these data show is there is a potential for a small risk for increased cancer and cancer deaths from Vytorin," Drazen tells WebMD. "Until clinical trials are completed, no one can say this drug is cleared -- and no one can say it causes cancer. We have to live with this uncertainty."
Assessing Cancer Risks
If there is a risk, it isn't very large, says Richard H. Karas, MD, PhD, director of preventive cardiology at Tufts Medical Center in Boston. Karas was not involved in the Pedersen or Peto studies, but he reviewed the published reports for WebMD.
In the SEAS trial, patients on placebo had a 0.5% annual risk of getting cancer. This risk doubled in patients on Vytorin -- but only to 0.9% a year. This risk was even lower in the two ongoing trials: 0.4% per year in control patients, and 0.5% per year in patients taking Vytorin.
But Peto tells WebMD that this risk -- if it were real -- would be frighteningly large. That's because it appeared in a very short time, in just the first years after patients began taking Vytorin. A real doubling of cancer risk in such a short time, he says, would make Vytorin one of the most dangerous carcinogens ever known.
But that, Peto says, is preposterous. When his team looked at the data from the IMPROVE-IT and SHARP trial, they found no increase in cancer over time -- which one would expect from a potent cancer-causing agent. Moreover, they found no increase in any specific kind of cancer.
"If this stuff was 100 times as dangerous as cigarette smoke, as the SEAS finding suggests, you would expect to see an increase over time in the hazard. And we don't," Peto tells WebMD. "And if you had no effect, you would expect the excess cases to be distributed evenly over time, and they are. So we do not get any increase over time in risk, either in cancer incidence or in death from cancer."
发布日期:2008-9-3
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