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5α-还原酶抑制剂治疗前列腺疾病:背景与实际意义

5alpha-Reductase inhibitor treatment of prostatic diseases: background and practical implications.

作者信息

Dörsam J, Altwein J

机构信息

St. Theresienkrankenhaus, Nürnberg, Germany.

出版信息

Prostate Cancer Prostatic Dis. 2009;12(2):130-6. doi: 10.1038/pcan.2008.56. Epub 2008 Nov 25.

Abstract

This literature review discusses the theoretical background of 5alpha-reductase inhibitor (5ARI) treatment and the resulting clinical implications. A Medline-based search for peer-reviewed articles addressing 5ARIs, benign prostatic hyperplasia and prostate cancer was performed. The 5ARIs Finasteride and Dutasteride, which specifically inhibit the production of dihydrotestosterone by acting as competitive inhibitors of 5alpha-reductase, are clinically well tolerated and represent an effective treatment option for benign prostatic obstruction. Finasteride is the first compound which has a proven efficacy in chemoprevention of prostate cancer. The aim of this review was to elucidate, if there are sufficient data available to point out clinically relevant differences between the drugs. Both compounds achieve a significant reduction of prostate volume, an improvement of symptoms and a lower risk of acute urinary retention. Whether the different pharmacokinetic and pharmacodynamic properties of Finasteride and Dutasteride are of clinical importance cannot be judged at this time.

摘要

本综述讨论了5α-还原酶抑制剂(5ARI)治疗的理论背景及其临床意义。通过基于Medline数据库检索同行评审的文章,以探讨5ARI、良性前列腺增生和前列腺癌。5ARI非那雄胺和度他雄胺通过作为5α-还原酶的竞争性抑制剂来特异性抑制二氢睾酮的产生,在临床上耐受性良好,是治疗良性前列腺梗阻的有效选择。非那雄胺是首个被证实对前列腺癌化学预防有效的化合物。本综述的目的是阐明是否有足够的数据指出这两种药物在临床上的相关差异。两种化合物均能显著缩小前列腺体积、改善症状并降低急性尿潴留的风险。目前尚无法判断非那雄胺和度他雄胺不同的药代动力学和药效学特性是否具有临床重要性。

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