This trial will evaluate the feasibility, toxicity, and efficacy of docetaxel/estramustine, as in the adjuvant therapy of patients with high-risk prostate cancer after definitive local therapy.
Upon determination of eligibility, patients will receive: Docetaxel + Estramustine
Study Type
INTERVENTIONAL
Allocation
NON_RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Enrollment
30
Tennessee Oncology, PLLC
Nashville, Tennessee, United States
Response Rate
Rate of recurrence
Toxicity
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