McVary Kevin T, Roehrborn Claus G, Kaminetsky Jed C, Auerbach Stephen M, Wachs Barton, Young Jay M, Esler Anne, Sides Gregory D, Denes Bela S
Department of Urology, Northwestern University Medical School, Chicago, Illinois 60611, USA.
J Urol. 2007 Apr;177(4):1401-7. doi: 10.1016/j.juro.2006.11.037.
We assessed the efficacy and safety of tadalafil dosed once daily for lower urinary tract symptoms secondary to benign prostatic hyperplasia.
Following a 4-week, single-blind, placebo run-in 281 men were randomly assigned (1:1) to 5 mg tadalafil for 6 weeks, followed by dose escalation to 20 mg for 6 weeks or 12 weeks of placebo.
Tadalafil significantly improved the mean change from baseline in International Prostate Symptom Score at 6 weeks (5 mg tadalafil -2.8 vs placebo -1.2) and at 12 weeks (5/20 mg tadalafil -3.8 vs placebo -1.7). Larger changes were observed with inclusion of the placebo run-in at 12 weeks (5/20 mg tadalafil -7.1 vs placebo -4.5). Significant improvements were also seen in the International Prostate Symptom Score irritative and obstructive domains, the International Prostate Symptom Score quality of life index, a question about urinary symptom improvement and the Benign Prostatic Hyperplasia Impact Index (significant at 12 weeks) vs placebo. International Prostate Symptom Score and International Index of Erectile Function erectile function domain scores significantly improved in the 56% of men with lower urinary tract symptoms/benign prostatic hyperplasia who were sexually active and had erectile dysfunction. Changes in uroflowmetry parameters were similar in the placebo and tadalafil groups. Commonly reported (2% or greater) treatment emergent adverse events were "erection increased," dyspepsia, back pain, headache, nasopharyngitis and upper respiratory tract infection (each 5.1% or less). No change in post-void residual volume was seen with tadalafil treatment.
Tadalafil once daily was well tolerated and demonstrated clinically meaningful and statistically significant symptomatic improvement for lower urinary tract symptoms/benign prostatic hyperplasia. Tadalafil also improved erectile function in men with lower urinary tract symptoms and erectile dysfunction.
我们评估了每日一次服用他达拉非治疗良性前列腺增生继发下尿路症状的疗效和安全性。
在为期4周的单盲安慰剂导入期后,281名男性被随机(1:1)分配接受5毫克他达拉非治疗6周,随后剂量增至20毫克再治疗6周,或接受12周的安慰剂治疗。
他达拉非在6周时显著改善了国际前列腺症状评分相对于基线的平均变化(5毫克他达拉非组为-2.8,安慰剂组为-1.2),在12周时也有显著改善(5/20毫克他达拉非组为-3.8,安慰剂组为-1.7)。在12周时纳入安慰剂导入期后观察到更大的变化(5/20毫克他达拉非组为-7.1,安慰剂组为-4.5)。国际前列腺症状评分的刺激性和梗阻性领域、国际前列腺症状评分生活质量指数、一个关于尿路症状改善的问题以及良性前列腺增生影响指数(在12周时显著)相对于安慰剂也有显著改善。在有下尿路症状/良性前列腺增生且有性功能障碍的56%的男性中,国际前列腺症状评分和国际勃起功能指数勃起功能领域评分显著改善。安慰剂组和他达拉非组的尿流率参数变化相似。常见的(2%或更高)治疗中出现的不良事件为“勃起增强”、消化不良、背痛、头痛、鼻咽炎和上呼吸道感染(各为5.1%或更低)。他达拉非治疗后残余尿量无变化。
每日一次服用他达拉非耐受性良好,对下尿路症状/良性前列腺增生有临床意义且具有统计学显著性的症状改善。他达拉非还改善了有下尿路症状和勃起功能障碍男性的勃起功能。