DETROIT, April 8, 2013 /PRNewswire-USNewswire/ -- Ulka Vaishampayan, M.D., leader of the Genitourinary Oncology Multidisciplinary Team at the Barbara Ann Karmanos Cancer Center, has contributed to an article just published in The New England Journal of Medicine comparing two different therapeutic methods in the treatment of metastatic, hormone-sensitive prostate cancer that becomes unresponsive to traditional methods of therapy. (Logo: http://photos.prnewswire.com/prnh/20071106/KARMANOSLOGO) The article is titled, "intermittent versus Continuous Androgen Deprivation in Hormone Sensitive Metastatic Prostate Cancer Patients: Results of S9346 (INT-0162) an International Phase III Trial." Fellow authors come from across America and internationally. The lead author, Maha Hussain, M.D., is from the University of Michigan. The Phase III trial began in 1995 and was completed in 2008 though patient follow-up has continued since completion. A total of 3,040 patients were accrued for the trial and 1,535 patients were randomized into receiving either complete androgen-deprivation therapy or intermittent androgen-deprivation therapy. Karmanos researchers recruited 112 patients onto the clinical trial, which represents one of the largest single institution accruals, according to Dr. Vaishampayan. The objective of the trial was to determine whether survival using intermittent androgen deprivation would provide better survival rates and quality of life for men compared to continuous androgen deprivation. Prostate cancer is an androgen-dependent disease and continuous androgen deprivation has been the standard therapy for metastatic (cancer that has spread), hormone-sensitive disease. Androgen is a male sex hormone, which includes testosterone. Researchers ultimately determined that intermittent androgen deprivation does not achieve comparable survival rates compared to complete androgen deprivation therapy, though it does provide small improvements in quality of life (i.e. emotional well-being and sexual function) for men with prostate cancer, but only in the first three months of receiving the intermittent therapy. Previous studies showed that intermittent androgen deprivation had prolonged the time between disease diagnosis and development of 'castrate-resistant' disease.