Guest guest Posted June 7, 2010 Report Share Posted June 7, 2010 A decade ago, a drug called Gleevec from Novartis SA electrified the cancer world with its ability to all but cure a deadly form of leukemia thanks to its effect on an aberrant gene known as the Philadelphia chromosome.  It helped transform cancer research into a hunt for genes and other biomarkers that might direct drug development and guide doctors in selecting treatments for their patients. At the meeting, study data showed that two second-generation drugs—Sprycel from Bristol-Myers Squibb and Tasigna, also from Novartis—outperformed Gleevec in certain measures of treating chromic myelogenous leukemia.  Assuming the drugs, now approved for patients who fail on Gleevec, gain approval for first-line treatment, physicians and patients will have alternatives to one of cancer's iconic drugs.  Gleevec " was such a revolutionary step, " says Mayer, vice president for academic affairs at Dana-Farber Cancer Institute, Boston. " It is encouraging that we can find ways to improve the product. "  Quote Link to comment Share on other sites More sharing options...
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