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抗雌激素药物和选择性雌激素受体调节剂可降低前列腺癌风险。

Antiestrogens and selective estrogen receptor modulators reduce prostate cancer risk.

作者信息

Steiner Mitchell S, Raghow Sharan

机构信息

Department of Urology, University of Tennessee, 1211 Union Avenue, Memphis, TN 38104, USA.

出版信息

World J Urol. 2003 May;21(1):31-6. doi: 10.1007/s00345-002-0316-x. Epub 2003 Feb 14.

Abstract

The development of chemoprevention strategies against prostate cancer would have the greatest overall impact both medically and economically against prostate cancer. Estrogens are required for prostate carcinogenesis. Estrogenic stimulation through estrogen receptor alpha in a milieu of decreasing androgens contributes significantly to the genesis of benign prostatic hyperplasia, prostate dysplasia, and prostate cancer. The ability of antiestrogens and selective estrogen receptor modulators (SERMs) to delay and to suppress prostate carcinogenesis is supported by preclinical, clinical, and epidemiological studies. SERMs have many features that make them attractive candidates for prostate cancer chemoprevention including their favorable safety profile and efficacy in preclinical prostate cancer models. The true clinical benefits of SERMs for chemoprevention to prevent prostate cancer, however, should continue to be investigated through human clinical trials. A phase IIb/III human clinical trial is currently evaluating safety and efficacy of toremifene, a SERM, in men who have high-grade prostatic intraepithelial neoplasia.

摘要

针对前列腺癌的化学预防策略的发展,在医学和经济方面对前列腺癌都将产生最大的总体影响。雌激素是前列腺癌发生所必需的。在雄激素水平降低的环境中,通过雌激素受体α的雌激素刺激对良性前列腺增生、前列腺发育异常和前列腺癌的发生有显著贡献。临床前、临床和流行病学研究均支持抗雌激素和选择性雌激素受体调节剂(SERM)延缓和抑制前列腺癌发生的能力。SERM具有许多特性,使其成为前列腺癌化学预防的有吸引力的候选药物,包括其良好的安全性和在临床前前列腺癌模型中的疗效。然而,SERM用于化学预防以预防前列腺癌的真正临床益处仍应通过人体临床试验继续进行研究。一项IIb/III期人体临床试验目前正在评估SERM托瑞米芬在患有高级别前列腺上皮内瘤变的男性中的安全性和疗效。

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