By Rob Stein
Washington Post / August 16, 2010
WASHINGTON — Federal regulators are considering taking the highly unusual step of rescinding approval of a drug that patients with advanced breast cancer turn to as a last-ditch hope.
The Food and Drug Administration is reviewing the recommendation of influential scientific advisers to revoke authorization of the drug to treat metastatic breast cancer. Contrary to initial research, new studies indicate that the benefits of the expensive drug, which costs $8,000 a month, do not outweigh its risks, the advisory panel concluded.
Citing a dearth of evidence of the drug’s effectiveness, its potential toxic side effects, and its high cost, many cancer specialists, patient advocates, and others are welcoming the prospect that Avastin’s authorization for breast cancer might be repealed. But the possibility is alarming other cancer specialists, women taking the drug, some members of Congress, and advocates for giving patients as much access to as many treatments as possible.
The FDA is not supposed to consider costs in its decisions, but if the agency were to rescind approval, insurers would be likely to stop paying for treatment.
“It’s hard to talk about Avastin without talking about costs,’’ said Eric Winer, director of the Breast Oncology Center at the Dana-Farber Cancer Institute in Boston. “For better or worse, Avastin has become in many ways the poster child of high-priced anticancer drugs.’’
Avastin is the best-selling cancer drug in the world, with global sales of $5.4 billion, and it is the best-selling product for Roche, whose Genentech unit makes it. Its use to treat breast cancer brings in about $8.5 million annually in US revenues.
Avastin was the first drug designed to fight cancer by blocking blood flow to tumors, which has been hailed as one of the first significant innovations in decades in the war on cancer. But Avastin is also one of the most expensive of a new generation of anticancer medications that only eke out a few extra months of life.
The FDA endorsed Avastin for advanced breast cancer in 2008 despite divided opinion about its usefulness for that purpose. Only one study had found that the drug appeared to delay an advanced breast tumor from growing by about five months. It remained unclear whether patients actually lived longer or experienced an improved quality of life.
But the FDA approved Avastin under a special program designed to make new treatments available as quickly as possible, with the caveat that pharmaceutical companies conduct follow-up studies validating their drug’s effectiveness. The agency has been criticized for failing to adequately review such approvals. Only one of at least 90 drugs that have received accelerated approval has been pulled.
An FDA advisory committee voted 12-1 July 20 to withdraw Avastin’s authorization for advanced breast cancer based on two new studies that the advisers concluded had failed to show the drug actually extends life.
“The vast majority opinion of the committee was that the drug was not doing very much, and what it was doing was more than offset by the negative,’’ said Wyndham Wilson of the National Cancer Institute, who chaired the committee. Avastin can cause a variety of potentially serious side effects, including blood clots, bleeding, and heart failure.
Why is this news for the EyeInfo blog? Avastin is also used to treat age related macular degeneration, and is quite effective at doing so. While we haven’t heard any news on it’s continued use in ophthalmology, we anxiously await to learn if they plan on revoking it in this field as well.
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