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度他雄胺和非那雄胺治疗良性前列腺增生症患者的疗效与安全性:一项系统评价和荟萃分析。

The efficacy and safety of dutasteride and finasteride in patients with benign prostatic hyperplasia: a systematic review and meta-analysis.

作者信息

Li Yao, Ma Jie, Qin Xin-Hua, Hu Chuan-Yi

机构信息

Department of Urology, Gongli Hospital Affiliated to Second Military Medical University, Shanghai, China.

出版信息

Transl Androl Urol. 2022 Mar;11(3):313-324. doi: 10.21037/tau-22-58.

Abstract

BACKGROUND

Although the efficacy and safety of monotherapy in the treatment of benign prostatic hyperplasia (BPH) have been established clinically, the efficacy and safety of dutasteride and finasteride have not been compared. The aim was to systematically evaluate the efficacy and safety of the two drugs in the treatment of BPH to provide medical evidence for clinical treatment.

METHODS

A search of relevant articles was conducted using the electronic databases PubMed, Embase, Medline, Cochrane Library, China Academic Journals Full-text Database (CJFD), Chinese Science and Technology Journal Database (VIP) and Wanfang Database. Randomized controlled trials (RCTs) comparing the efficacy of finasteride (control group) with that of dutasteride (experimental group) in the treatment of BPH with respect to the International Prostate Symptom Score (IPSS), the maximum urinary flow rate (Qmax), prostate volume (PV), quality of life (QOL), serum prostate-specific antigen (PSA) level and adverse drug reactions (ADRs) after medication were strictly evaluated and considered for inclusion. Rev Man 5.4 software was used for the meta-analysis.

RESULTS

A total of 8 RCTs were included, with a total of 2,116, patients. The meta-analysis showed that compared with finasteride, dutasteride can effectively improve the Qmax of patients with BPH [mean difference (MD) =0.32; 95% confidence interval (CI): (0.01, 0.63); P=0.04]. There was no significant difference in reducing IPSS [MD =0.13; 95% CI: (-0.55, 0.82); P=0.70], improving PV [MD =-1.25; 95% CI: (-3.30, 0.79); P=0.23], reducing QOL [MD =-0.44; 95% CI: (-0.93, 0.05); P=0.08] and serum PSA level [MD =-0.04; 95% CI: (-0.15, 0.07); P=0.50], and the occurrence of ADRs [relative risk (RR) =-0.01; 95% CI: (-0.05, 0.04); P=0.72], there was no significant difference.

DISCUSSION

Dutasteride is better than finasteride in improving the Qmax of patients with BPH. There was no statistically significant difference in symptoms, PV, PSA, QOL, or adverse reactions. Dutasteride is an effective and safe treatment for BPH. Due to the limitations of the methodological quality and sample size of the included studies, this conclusion needs to be verified by stratified RCTS with high volumes and long follow-up times.

摘要

背景

虽然单一疗法治疗良性前列腺增生(BPH)的疗效和安全性已在临床上得到证实,但度他雄胺和非那雄胺的疗效和安全性尚未进行比较。目的是系统评价这两种药物治疗BPH的疗效和安全性,为临床治疗提供医学依据。

方法

使用电子数据库PubMed、Embase、Medline、Cochrane图书馆、中国学术期刊全文数据库(CJFD)、中国科技期刊数据库(VIP)和万方数据库检索相关文章。严格评估并纳入比较非那雄胺(对照组)和度他雄胺(试验组)治疗BPH在国际前列腺症状评分(IPSS)、最大尿流率(Qmax)、前列腺体积(PV)、生活质量(QOL)、血清前列腺特异性抗原(PSA)水平及用药后药物不良反应(ADR)方面疗效的随机对照试验(RCT)。采用Rev Man 5.4软件进行荟萃分析。

结果

共纳入8项RCT,患者总数为2116例。荟萃分析显示,与非那雄胺相比,度他雄胺可有效改善BPH患者的Qmax[平均差(MD)=0.32;95%置信区间(CI):(0.01,0.63);P=0.04]。在降低IPSS[MD =0.13;95%CI:(-0.55,0.82);P=0.70]、改善PV[MD =-1.25;95%CI:(-3.30,0.79);P=0.23]、降低QOL[MD =-0.44;95%CI:(-0.93,0.05);P=0.08]和血清PSA水平[MD =-0.04;95%CI:(-0.15,0.07);P=0.50]以及ADR的发生[相对危险度(RR)=-0.01;95%CI:(-0.05,0.04);P=0.72]方面,无显著差异。

讨论

度他雄胺在改善BPH患者Qmax方面优于非那雄胺。在症状、PV、PSA、QOL或不良反应方面无统计学显著差异。度他雄胺是治疗BPH的一种有效且安全的药物。由于纳入研究的方法学质量和样本量存在局限性,这一结论需要通过大样本量和长时间随访的分层RCT进行验证。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ad4b/8984969/e4d1490a1adb/tau-11-03-313-f1.jpg

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