Men with metastatic prostate cancer treated with androgen ablation respond
rapidly and often dramatically to therapy, with improvement of bone pain, r
egression of soft tissue metastases, and declines in serum prostate-specifi
c antigen (PSA). Unfortunately, few treatment options are available to men
who progress after hormone therapy. Recent studies in the mechanism of anti
cancer drug action have focused on the proteins that regulate apoptosis or
programmed cell death as a target for the treatment of hormone-resistant pr
ostate cancer. New treatments are now being designed with both resistance a
nd apoptotic pathways in mind. US Food and Drug Administration (FDA) approv
al of the combination of mitoxantrone and prednisone for the palliation of
bone pain in men with hormone refractory prostate cancer demonstrates that
chemotherapy can be effective. Two randomized trials have demonstrated the
superiority of mitoxantrone combined with a corticosteroid over corticoster
oid therapy in alleviating bone pain. The combination of estramustine with
vinblastine, or VP-16, is commonly used in clinical practice with both regi
mens demonstrating significant PSA declines. When estramustine is combined
with either paclitaxel or docetaxel in vitro, greater than additive in vitr
o cytotoxicity is noted. Phase I and II studies of taxane-based therapy in
hormone refractory prostate cancer demonstrate improved survival when compa
red with historical controls, but phase III studies are necessary to confir
m these preliminary observations. (C) 1999, Elsevier Science Inc.