Jl. Mohler et al., COUMARIN (1,2-BENZOPYRONE) FOR THE TREATMENT OF PROSTATIC-CARCINOMA, Journal of cancer research and clinical oncology, 120, 1994, pp. 35-38
The unavailablility of effective treatment for metastatic hormone-refr
actory and clinically localized but pathologically unfavorable prostat
ic carcinoma warrants trial of new and promising treatments. Prelimina
ry studies in patients with metastatic disease have shown (a) subjecti
ve but no objective responses to 100 mg coumarin and cimetidine daily;
(b) objective responses in 3 of 40 patients treated with 3 g coumarin
daily, all of whom had normal performance status and 1 of whom remain
s with three resolved bone metastases and stable prostate-specific ant
igen levels after 4 years; (c) toxicity only in bedridden patients. We
recently initiated two multi-center trials of 1 g coumarin daily. Met
astatic prostatic carcinoma patients of normal performance status were
treated in a phase II trial. Patients who had been treated by radical
prostatectomy, but had surgical margin, seminal vesicle or lymph node
involvement or detectable prostate-specific antigen after radical pro
statectomy, were randomized to coumarin or placebo.