To compare overall survival after receiving mitoxantrone and prednisone or docetaxel and prednisone in subjects with hormone-refractory metastatic prostate cancer.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Enrollment
228
75mg/m² intravenously (day 1) every 21 days
12mg/m² intravenously every 21 days
10mg orally given daily
Sanofi-Aventis Administrative Office
Shanghai, China
Efficacy: Overall survival
Time frame: From beginning to end of the study
Objective response rate of patients with measurable disease by Response Evaluation Criteria in Solid tumours
Time frame: From beginning to end of study
Prostatic Specific Antigen response
Time frame: From the beginning to the end of study
Pain response (McGill-Melzack Scale)
Time frame: From beginning to end of study
Time to progression
Time frame: From beginning to end of study
Adverse event
Time frame: From beginning to end of study
Quality Of Life: Functional assessment of chronic illness therapy-prostate questionnaire will be used
Time frame: From beginning to end of study
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