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    Genetic Key to Lung Cancer Drug Success Found

    Genetic Screening May Allow Targeted, Effective Lung Cancer Treatment

    WebMD Health News

    April 30, 2004 -- A new discovery may soon allow doctors to target lung cancer therapy based on a person's genetic profile.

    Lung cancer is the leading cause of cancer death in the U.S., and until now no effective treatments have been available for the disease. A recently approved drug, Iressa, is thought to be the first drug to work well against lung cancer, but the problem is that it works only in a small number of people.

    However, two new studies show that genetic screening may help doctors identify which lung cancer patients will respond well to the drug as a first line of treatment. Researchers found people with non-small-cell lung cancer that had an abnormal gene for the epidermal growth factor receptor (EGFR) benefited dramatically from treatment with Iressa.

    Non-small-cell lung cancer accounts for the majority of lung cancer cases and deaths. In people with this type of cancer, EGF (epidermal growth factor) causes cells to grow and form a solid tumor.

    "We know that many lung cancers have elevated EGFR expressions, but only a few thus far have been shown to respond to Iressa," says Harmon Eyre, MD, chief medical officer of the American Cancer Society, in a news release. "This study indicates potentially better outcomes for 10 to 15 percent of those diagnosed with non-small cell lung cancer, primarily non-smoking women, and while it may not have a huge impact in terms of sheer numbers, it is a major step."

    The findings appear in this week's issue of the journal Science and in an upcoming issue of The New England Journal of Medicine (NEJM).

    Targeted Lung Cancer Therapies Now a Possibility

    In the studies, researchers compared the genetic makeup of lung cancer tumors extracted from people who were treated with Iressa, including those who had responded well to the drug and those that didn't.

    They found those that had responded well to the drug were much more likely to share the same genetic mutation of the EGFR gene. For example, Thomas Lynch, MD, and colleagues at Harvard Medical School, reported in NEJM that eight of nine patients who were successfully treated with the drug had the mutation while none of the seven that didn't respond to the drug had it.

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