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5α-还原酶抑制剂/非那雄胺

5alpha-reductase inhibitors/finasteride.

作者信息

Stoner E

机构信息

Merck Research Laboratories, Department of Clinical Research, Rahway, New Jersey 07065-0900, USA.

出版信息

Prostate Suppl. 1996;6:82-7.

PMID:8630236
Abstract

Benign prostatic hyperplasia (BPH) is a disease diagnosed by the presence of prostatic enlargement and lower-tract urinary obstruction. Finasteride (Proscar), is a potent and specific inhibitor of 5alpha-reductase, which inhibits the conversion of testosterone (T) to dihydrotestosterone (DHT) an important promoter of prostatic growth. It has provided a new therapeutic alternative for the treatment of BPH. The safety and efficacy of finasteride in the treatment of symptomatic BPH have been demonstrated by two multi-center placebo-controlled studies. After 12 months of treatment with 5 mg finasteride daily, prostate volume, DHT and prostate-specific antigen (PSA) levels were reduced and maximum urinary flow rates and symptom scores were improved. Finasteride was well-tolerated. Upon completion of the controlled studies, patients were eligible to enter an open-label extension study in which all patients received 5 mg finasteride. Approximately half of the 543 patients randomized to the 5 mg finasteride group in the controlled studies have now been treated with 5 mg finasteride continuously for 3 years. The data provided by this group of patients on the long-term safety and efficacy of finasteride in the treatment of symptomatic BPH are reviewed.

摘要

良性前列腺增生(BPH)是一种通过前列腺增大和下尿路梗阻来诊断的疾病。非那雄胺(保列治)是一种强效且特异性的5α-还原酶抑制剂,它可抑制睾酮(T)向双氢睾酮(DHT)的转化,而双氢睾酮是前列腺生长的重要促进因子。它为BPH的治疗提供了一种新的治疗选择。两项多中心安慰剂对照研究已证实了非那雄胺治疗有症状BPH的安全性和有效性。每天服用5毫克非那雄胺治疗12个月后,前列腺体积、双氢睾酮和前列腺特异性抗原(PSA)水平降低,最大尿流率和症状评分得到改善。非那雄胺耐受性良好。对照研究完成后,患者有资格进入开放标签扩展研究,所有患者均接受5毫克非那雄胺治疗。在对照研究中随机分配到5毫克非那雄胺组的543名患者中,约有一半目前已连续服用5毫克非那雄胺3年。本文回顾了这组患者提供的关于非那雄胺治疗有症状BPH的长期安全性和有效性的数据。

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