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Chemotherapy drugs show promise against skin cancer

By Suzanne Rostler

NEW YORK, Jun 28 (Reuters Health) - A combination of two chemotherapy drugs appears to prolong the lives of patients with high risk for a recurrence of the deadly skin cancer melanoma, results of a preliminary study suggest. According to researchers with the University of California at San Diego (UCSD), tamoxifen, a drug used to treat breast cancer, and cisplatin, another cancer chemotherapy drug, extended the lives of patients with melanoma who were at high risk for recurrence.

When diagnosed early, melanoma is curable. But many cases are not diagnosed with melanoma until the cancer has spread (metastasized), dramatically reducing the chances for survival and increasing the risk that the cancer will come back, or recur, after initial treatment.

"If it recurs, it often does so with a much more aggressive and lethal personality," lead author Dr. Edward F. McClay of the UCSD Cancer Center, said in a statement. "These statistics, while preliminary, are very encouraging because we have had precious little to offer patients with metastatic melanoma," he added.

The current standard therapy to treat patient with high-risk melanoma is interferon, a growth factor that stimulates the immune system to seek out and kill melanoma cells. However, only about 35% of patients who are treated with interferon survive for five years, McClay told Reuters Health. His study in the British Journal of Cancer found that 85% of patients were alive and 68% of patients were free of cancer three years after treatment with the tamoxifen/cisplatin therapy. Based on these results, researchers predict that 79% of patients will survive and 62% of patients will not have a tumor recurrence after five years.

However, it is still not clear how the drug combination works. Alone, neither drug has proven effective against melanoma, the authors note. "We haven't finished working out the mechanism but it appears that tamoxifen stimulates growth factors in many cancer cells which may interact with cisplatin and makes the cancer cells easier to kill," McClay said. The researchers treated 153 patients who had undergone surgery to remove their cancer but remained at risk for recurrence, or whose cancer had already recurred. Patients received tamoxifen for seven days and on the second day they received a dose of cisplatin. The week-long regimen was given once a month for four months. McClay stressed that researchers will need to conduct larger trials before the drugs are given to patients with high-risk melanoma outside of clinical studies.

"If it works, it is going to be huge because it substantially lowers the death and recurrence rate, but that is what needs to be confirmed," McClay said.


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