The purpose of this study is to evaluate the safety of docetaxel administered every 3 weeks repeatedly for 11 and more cycles and in combination with daily prednisolone for metastatic hormone refractory prostate cancer.
Study Type
INTERVENTIONAL
Allocation
NON_RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Enrollment
16
combined treatment with prednisolone
Sanofi-Aventis Administrative Office
Tokyo, Japan
Incidence rate of adverse events on each grade evaluated by National Cancer Institute Common Toxicity Criteria (Version 2.0)
Time frame: First treatment up to 37 months
No obvious disease progression
Time frame: First treatment up to 37 months
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