A comparison of the efficacy and tolerability of tamsulosin and finasteride in patients with lower urinary tract symptoms suggestive of benign prostatic hyperplasia

被引:24
作者
Rigatti, P
Brausi, M
Scarpa, RM
Porru, D
Schumacher, H
Rizzi, CA
机构
[1] Univ Vita Salute San Raffaele, Urol Clin, I-20132 Milan, Italy
[2] Osped Estense S Agostino, Modena, Italy
[3] Osped S Luigi Gonzaga, Orbassano, Italy
[4] Policlin San Matteo, I-27100 Pavia, Italy
[5] Boehringer Ingelheim Pharma GmbH & Co KG, Ingelheim, Germany
[6] Boehringer Ingelheim Italy SpA, Milan, Italy
关键词
prostatic hyperplasia; adrenergic alpha-antagonists; tamsulosin; finasteride; randomised controlled trial;
D O I
10.1038/sj.pcan.4500680
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
In this multicentre, double-blind study, patients with LUTS/BPH were randomised to 26 weeks with finasteride 5 mg once daily (n - 204) or tamsulosin 0.4 mg once daily (n = 199). Double-blind treatment was continued for another 26 weeks (total treatment duration: 1y). The primary efficacy parameter was the difference in mean change in total Symptom Problem Index (SPI) from baseline to end point at week-26 in the intention-to-treat (ITT) and per protocol (PP) populations. Tamsulosin induced a greater improvement in total SPI (-5.2 points or -37%) compared to finasteride (-4.5 points or -31%) at week-26 (P = 0.055 in ITT and P = 0.032 in PP). Tamsulosin improved urinary symptoms (particularly the more bothersome storage symptoms) and flow more quickly than finasteride. The difference was statistically significant for the SPI from week-1 (reduction, respectively, -2.5 vs -1.8 points, P = 0.043) to week-18 and for Q(max) from week-1 (increase, respectively, 2.3 vs 0.7 ml/s, P = 0.0007) to week-12. Both treatments were well tolerated with a comparable incidence of adverse events, including urinary retention.
引用
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页码:315 / 323
页数:9
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