Paclitaxel, estramustine, and etoposide in the treatment of hormone-refractory prostate cancer.

Abstract

We previously developed a novel and effective therapy for hormone-refractory prostate cancer using the agents estramustine and etoposide. Although neither of these agents alone is effective in the treatment of advanced, hormone-refractory prostate cancer, we predicted their activity when used in combination based on preclinical assays, and then demonstrated their effectiveness in a phase I-II clinical trial, where they were shown to produce a 50% complete and partial response rate in patients with bidimensionally measurable disease. In preclinical studies, we had demonstrated that estramustine and etoposide interact with the nuclear matrix, which is the site of DNA replication. Expanding these investigations, we determined that paclitaxel (Taxol; Bristol-Myers Squibb Company, Princeton, NJ), a microtubule inhibitor, interacts with estramustine and etoposide, and the combination of these three agents had significant preclinical activity against androgen-independent prostate cancer cells. These studies led us to conduct a phase II clinical trial of paclitaxel, estramustine, and etoposide in patients with hormone-refractory prostate cancer. Preliminary results demonstrate that this is an active regimen, with 57% of patients demonstrating a response to therapy as measured by a decrease in pretreatment prostate-specific antigen levels of greater than 50%.

• Authors: K J Pienta, D C Smith
• Journal: Seminars in oncology (Semin Oncol) Vol. 24 Issue 5 Suppl 15 Pg. S15-72-S15-77 (Oct 1997) ISSN: 0093-7754 [Print] United States
• PMID: 9346227 (Publication Type: Clinical Trial, Clinical Trial, Phase I, Clinical Trial, Phase II, Journal Article)

Chemical References

• Antineoplastic Agents, Hormonal
• Antineoplastic Agents, Phytogenic
• DNA, Neoplasm
• Estramustine
• Etoposide
• Prostate-Specific Antigen
• Paclitaxel

Topics

• Adenocarcinoma (drug therapy, pathology)
• Administration, Oral
• Alopecia (chemically induced)
• Animals
• Antineoplastic Agents, Hormonal (administration & dosage, adverse effects, therapeutic use)
• Antineoplastic Agents, Phytogenic (administration & dosage, adverse effects)
• Antineoplastic Combined Chemotherapy Protocols (administration & dosage, adverse effects, therapeutic use)
• DNA Replication (drug effects)
• DNA, Neoplasm (drug effects)
• Disease Progression
• Drug Administration Schedule
• Drug Resistance, Neoplasm
• Drug Screening Assays, Antitumor
• Estramustine (administration & dosage, adverse effects)
• Etoposide (administration & dosage, adverse effects)
• Follow-Up Studies
• Humans
• Infusions, Intravenous
• Male
• Microtubules (drug effects)
• Nuclear Matrix (drug effects)
• Paclitaxel (administration & dosage, adverse effects)
• Prostate-Specific Antigen (analysis)
• Prostatic Neoplasms (drug therapy, pathology)
• Rats
• Remission Induction
• Tumor Cells, Cultured