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ASCO: Abiraterone Tolerated in High-Risk Prostate Cancer

Thursday, May 17, 2012 (Last Updated: 05/18/2012)

THURSDAY, May 17 (HealthDay News) -- For men with localized high-risk prostate cancer, neoadjuvant androgen deprivation therapy with abiraterone acetate (AA) plus leuprolide acetate (LHRHa) is well tolerated and has good pathological complete/near complete response (pCR/near pCR) rates, according to a study released May 16 in advance of presentation at the annual meeting of the American Society of Clinical Oncology, held from June 1 to 5 in Chicago.

Mary-Ellen Taplin, M.D., from Harvard Medical School and the Dana-Farber Cancer Institute in Boston, and colleagues conducted a randomized phase II trial for neoadjuvant AA/LHRHa in 58 men (median age, 58 years) with localized high-risk prostate cancer. Participants were randomly allocated to receive LHRHa (28 men) or AA/LHRHa/prednisone (30 men) for 12 weeks. After 12 weeks, all men received AA/LHRHa/prednisone for a further 12 weeks, followed by radical prostatectomy.

The researchers found that the pCR/near pCR was 25 percent overall, and was 34 percent for those treated with AA for 24 weeks and 15 percent for those treated with AA for 12 weeks. Grade 3 elevated aspartate aminotransferase/alanine aminotransferase and hypokalemia were seen in 9 and 5 percent of patients, respectively, and no grade 4 mineralocorticoid-related adverse events were observed.

"For this proportion of patients with high-risk disease to have very little to no detectable cancer in the prostate after six months of therapy is dramatic," Taplin said in a statement. "Our findings suggest that this combination therapy approach could improve outcomes for a substantial number of men, but larger, long-term trials are needed to confirm this approach."

Several authors disclosed financial ties to pharmaceutical companies, including Johnson & Johnson, which manufactures abiraterone acetate.

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Specialties Hematology & Oncology

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