Cancer Drugs Could Save Thousands
September 8, 2003
The Food and Drug Administration (FDA) is often praised for establishing the "gold standard" for drug approval where adherence to regulations and policy is strict and absolute. All FDA approved drugs have been rigorously shown to be safe and effective through years of careful review.
However, some critics charge the FDA has failed to keep up with the fast pace of cancer research in ways that might allow thousands of patients to benefit from promising new cancer medications that are still in the approval process. For instance, about 57,000 people die of colon cancer each year. There are two drugs that might benefit some colon cancer patients, but approval is not expected until 2004.
- The cancer drug Erbitux has been shown to shrink tumors in about one-quarter of patients for which nothing else would work and extends life by about four months. Although rejected in 2001, it more than meets the FDA's current standards for accelerated approval.
- The experimental colon cancer drug Avastin, when combined with first-line treatments known as the Saltz regimen, extends the effectiveness of treatments (and patient survival) by more than four months.
Prior to approval, only the small number of patients able to sign up for clinical trials will benefit from them. Companies shepherding drugs through the approval process cannot legally sell drugs to desperate patients wishing to participate (but unable to enroll) in clinical trials. Neither can drug companies afford to donate drugs free of charge to thousands of patients not officially participating in the expensive, closely monitored drug trails.
The Abigail Alliance for Better Access to Developmental Drugs thinks it has a solution called "Tier 1 Initial Approval." This would allow patients limited access to experimental drugs that have initially shown to be effective but are possibly months away from "full" FDA approval.
Source: Steven Walker, "S.O.S. to the FDA," Wall Street Journal, August 26, 2003.
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