Guest guest Posted March 10, 2008 Report Share Posted March 10, 2008 http://www.nytimes.com/2008/03/10/opinion/10mon2.html?ex=1205812800 & en=34e2a0cff3bde690 & ei=5070 & emc=eta1 SNIP The key study showed that when used with another drug, Avastin almost doubled the time cancers were held in check before starting to worsen. It also doubled the number of women whose tumors shrank significantly. It did not extend overall survival rates and caused more serious side effects, including perhaps half a dozen deaths. That seems like a modest basis for approval pending completion of additional clinical trials. The quandary is whether an extra 5 1/2 months of holding tumor progression at bay is worth toxic side effects. The drug is already prescribed “off label” for some 11,000 American women with advanced breast cancer, but the latest approval is expected to increase its use among some 43,000 women deemed suitable candidates for treatment. The cost could be enormous. Genentech charges about $92,000 a year for breast cancer patients. For women with annual family incomes below about $100,000, it caps the charges at $55,000 a year. The company argues that Avastin emerged from many years of costly research. It does not claim that the drug is cost-effective for advanced breast cancer but believes it will clearly be worth the cost if shown effective in earlier stages of breast cancer. Britain’s National Health Service has balked at paying for Avastin for breast cancer patients. If this country hopes to get escalating health care costs under control, it will need a way to determine which treatments are worth paying for, and which are not. The case of Avastin is a reminder of just how difficult that can be. Quote Link to comment Share on other sites More sharing options...
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