Cui Jianwei, Cao Dehong, Bai Yunjin, Wang Jiahao, Yin Shan, Wei Wuran, Xiao Yunfei, Wang Jia, Wei Qiang
Department of Urology, Institute of Urology, West China Hospital of Sichuan University, Chengdu, China.
Front Med (Lausanne). 2021 Oct 12;8:744012. doi: 10.3389/fmed.2021.744012. eCollection 2021.
Tadalafil has been approved for the treatment of benign prostatic hyperplasia (BPH) for nearly 10 years. However, there are insufficient evidence-based studies of the efficacy and safety of tadalafil in treating lower urinary tract symptoms of BPH (LUTS/BPH). To evaluate the therapeutic effect and clinical safety of tadalafil monotherapy (5 mg once daily for 12 weeks) for LUTS/BPH. A total of 13 studies (15 randomized clinical trials [RCTs]) were extracted from the following databases: PubMed, Cochrane Central Register of Controlled Trials, Embase, and Web of Science for the period up to July 2021. The quality of the included RCTs was evaluated independently by two authors, who, respectively, extracted data according to the Preferred Reporting Items for Systematic Reviews and Meta-Analyses principles. Conflicts were settled by a discussion with two-third of senior authors. All data analyses were conducted by the Review Manager, version 5.4. Regarding efficacy, 12-week trials indicated that 5 mg once daily tadalafil showed a significantly lower and, consequently, better total International Prostate Symptom Score (IPSS) than the placebo did (mean difference [MD]: -1.97, 95% CI: -2.24 to -1.70; < 0.00001). In addition, significant differences were found between the tadalafil regimen and the placebo in the IPSS voiding subscore (MD: -1.30, 95% CI: -1.48 to -1.11; < 0.00001), the IPSS storage subscore (MD: -0.70, 95% CI: -0.82 to -0.58; < 0.00001), the IPSS quality of life (MD: -0.29, 95% CI: -0.35 to -0.22; < 0.00001), and BPH impact index (MD: -0.58, 95% CI: -0.76 to -0.40; < 0.00001). The safety analysis did not show a significant difference in serious adverse events between the two groups (risk ratio: 1.27, 95% CI: 0.80-2.01; = 0.31), although the adverse events occurred at a higher incidence in the tadalafil group than in the placebo. This study demonstrates that once daily 5 mg tadalafil is a potentially effective and safe treatment choice with excellent tolerability for patients with LUTS/BPH. Identifier (CRD42021228840).
他达拉非已被批准用于治疗良性前列腺增生(BPH)近10年。然而,关于他达拉非治疗BPH下尿路症状(LUTS/BPH)的疗效和安全性,基于证据的研究并不充分。为评估他达拉非单药治疗(每日5毫克,持续12周)对LUTS/BPH的治疗效果和临床安全性。从以下数据库中提取了总共13项研究(15项随机临床试验[RCT]):截至2021年7月的PubMed、Cochrane对照试验中央注册库、Embase和科学网。两名作者分别根据系统评价和Meta分析的首选报告项目独立评估纳入RCT的质量,并提取数据。如有分歧,将与三分之二的资深作者进行讨论解决。所有数据分析均使用Review Manager 5.4版进行。关于疗效,12周的试验表明,每日一次5毫克他达拉非的总国际前列腺症状评分(IPSS)显著低于安慰剂,因此效果更好(平均差值[MD]:-1.97,95%置信区间:-2.24至-1.70;P<0.00001)。此外,他达拉非治疗方案与安慰剂在IPSS排尿子评分(MD:-1.30,95%置信区间:-1.48至-1.11;P<0.00001)、IPSS储尿子评分(MD:-0.70,95%置信区间:-0.82至-0.58;P<0.00001)、IPSS生活质量评分(MD:-0.29,95%置信区间:-0.35至-0.22;P<0.00001)和BPH影响指数(MD:-0.58,95%置信区间:-0.76至-0.40;P<0.00001)方面存在显著差异。安全性分析显示,两组严重不良事件无显著差异(风险比:1.27,95%置信区间:0.80-2.01;P=0.31),尽管他达拉非组不良事件的发生率高于安慰剂组。本研究表明,对于LUTS/BPH患者,每日一次5毫克他达拉非是一种潜在有效且安全的治疗选择,耐受性良好。标识符(CRD42021228840)。