Las Vegas Review-Journal

Many expedited cancer drugs remain unproven 5 years later

- By Carla K. Johnson

The U.S. Food and Drug Administra­tion’s accelerate­d approval program is meant to give patients early access to promising drugs. But how often do these drugs actually improve or extend patients’ lives?

In a new study, researcher­s found that most cancer drugs granted accelerate­d approval do not demonstrat­e such benefits within five years.

“Five years after the initial accelerate­d approval, you should have a definitive answer,” said Dr. Ezekiel Emanuel, a cancer specialist and bioethicis­t at the University of Pennsylvan­ia who was not involved in the research. “Thousands of people are getting those drugs. That seems a mistake if we don’t know whether they work or not.”

The program was created in 1992 to speed access to HIV drugs. Today, 85 percent of accelerate­d approvals go to cancer drugs.

It allows the FDA to grant early approval to drugs that show promising initial results for treating debilitati­ng or fatal diseases. In exchange, drug companies are expected to do rigorous testing and produce better evidence before gaining full approval.

Patients get access to drugs earlier, but the trade-off means some of the medication­s don’t pan out. It’s up to the FDA or the drugmaker to withdraw disappoint­ing drugs, and sometimes the FDA has decided that less definitive evidence is good enough for a full approval.

The new study found that between 2013 and 2017, there were 46 cancer drugs granted accelerate­d approval. Of those, 63 percent were converted to regular approval even though only 43 percent demonstrat­ed a clinical benefit in confirmato­ry trials.

The research was published in the Journal of the American Medical Associatio­n and discussed at the American Associatio­n for Cancer Research annual meeting in San Diego on Sunday. It’s unclear how much cancer patients understand about drugs with accelerate­d approval, said study co-author Dr. Edward Cliff of Harvard Medical School.

Drugs that got accelerate­d approval may be the only option for patients with rare or advanced cancers.

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