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Cited by 200

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Estramustine and Vinblastine: Use of Prostate Specific Antigen as a Clinical Trial End Point for Hormone Refractory Prostatic Cancer

Seidman, Andrew D., Scher, Howard I., Petrylak, Daniel, Dershaw, D. David, Curley, Tracy·1992·Journal of Urology

Abstract

The combination of estramustine phosphate and vinblastine sulfate, 2 agents with separate and unique antimicrotubular effects, has demonstrated additive cytotoxicity against the DU145 human prostate derived cell line in vitro. We evaluated this combination in 25 patients with progressive hormone refractory prostate cancer. Of 24 patients with an elevated prostate specific antigen (PSA) level at the start of treatment 13 (54%, 95% confidence limits 34 to 74%) had a greater than 50% decrease in PSA levels on at least 3 consecutive biweekly determinations. The median decrease in PSA in responding patients was 64% (mean 71.7%) and the median duration of response was 7 months. In 5 patients with bidimensionally measurable disease 2 partial responses were observed. Treatment was well tolerated, with mild and manageable toxicity. This is a well tolerated outpatient treatment regimen for patients with hormone-refractory prostatic cancer which deserves further investigation.

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Metadata

Authors
Seidman, A. D., Scher, H. I., Petrylak, D., Dershaw, D. D., & Curley, T.
Venue
Journal of Urology
Published
1992-03
Volume
147
Issue
3 Part 2
Pages
931-934
ISSN
  • 0022-5347 (ISSN-L)
  • 1527-3792
OpenAlex
W2415683488
Cited by
200
References
0
FWCI
15.19
Type
journal article
Language
en
Open access
closed

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CoChat. (2026). Citation check: Estramustine and Vinblastine: Use of Prostate Specific Antigen as a Clinical Trial End Point for Hormone Refractory Prostatic Cancer. https://app.cochat.ai/papers/10.1016/s0022-5347(17)37426-8
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Seidman, A. D., Scher, H. I., Petrylak, D., Dershaw, D. D., & Curley, T. (1992). Estramustine and Vinblastine: Use of Prostate Specific Antigen as a Clinical Trial End Point for Hormone Refractory Prostatic Cancer. Journal of Urology. https://doi.org/10.1016/s0022-5347(17)37426-8

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Contains information from the Semantic Scholar Academic Graph Datasets, made available under the ODC Attribution License (ODC-BY 1.0).

Semantic Scholar’s data is described in: Kinney, R., et al. (2023). The Semantic Scholar Open Data Platform. arXiv:2301.10140.