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Multicenter Phase II study of estramustine phosphate plus weekly paclitaxel in patients with androgen-independent prostate carcinoma

โœ Scribed by David J. Vaughn; Archie W. Brown Jr.; W. Graydon Harker; Sang Huh; Lance Miller; David Rinaldi; Fairooz Kabbinavar


Publisher
John Wiley and Sons
Year
2004
Tongue
English
Weight
72 KB
Volume
100
Category
Article
ISSN
0008-543X

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โœฆ Synopsis


Abstract

BACKGROUND

The current study determined the efficacy and toxicity of weekly paclitaxel in combination with estramustine phosphate (EMP) in patients with androgenโ€independent prostate carcinoma (AIPC).

METHODS

Patients with progressive AIPC received 90 mg/m^2^ paclitaxel by 1โ€hour intravenous infusion weekly for 3 weeks, followed by a 1โ€week treatment rest. Patients received 140 mg EMP orally 3 times daily on the day before, the day of, and the day after paclitaxel administration. Patients received 1 mg warfarin daily to prevent thromboembolism.

RESULTS

Sixtyโ€six patients with progressive AIPC received treatment at 29 centers. Fortyโ€two percent of patients had a 50% decline in prostateโ€specific antigen (PSA; 95% confidence interval [CI], 30โ€“54%). For 26 patients with bidimensionally measurable disease, the objective response rate was 15% (95% CI, 1โ€“30%). The median time to disease progression was 6.3 months, and the median time to PSA progression was 11.4 months. The median survival period was 15.6 months. Grade 3โ€“4 toxicities were uncommon and included thromboembolism (8%), anemia (3%), neutropenia (3%), and peripheral neuropathy (2%). There was one treatmentโ€related death.

CONCLUSIONS

This regimen of EMP plus weekly paclitaxel was an active and well tolerated treatment for patients with AIPC. Cancer 2004;100:746โ€“50. ยฉ 2004 American Cancer Society.


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