Division of Urology, Department of Surgery, University of Toronto, University Health Network, 610 University Avenue, 3-130, Toronto, Ontario, Canada M5G 2M9.
BMJ. 2013 Apr 15;346:f2109. doi: 10.1136/bmj.f2109.
To assess the role of dutasteride in preventing clinical progression of benign prostatic hyperplasia in asymptomatic men with larger prostates.
Post hoc analysis of four year, double blind Reduction by Dutasteride of Prostate Cancer Events (REDUCE) study
1617 men randomised to dutasteride or placebo with a prostate size >40 mL and baseline International Prostate Symptom Score (IPSS) <8. Subjects who took medications for benign prostatic hyperplasia were excluded at study entry.
Placebo or dutasteride 0.5 mg daily.
Comparison of risk of clinical progression of benign prostatic hyperplasia at four years (defined as a ≥ 4 point worsening on IPSS, acute urinary retention, urinary tract infection, or surgery related to benign prostatic hyperplasia).
825 participants took placebo, 792 took dutasteride. A total of 464 (29%) experienced clinical progression benign prostatic hyperplasia, 297(36%) taking placebo, 167 (21%) taking dutasteride (P<0.001). The relative risk reduction was 41% and the absolute risk reduction 15%, with a number needed to treat (NNT) of 7. Among men who had acute urinary retention and surgery related to benign prostatic hyperplasia, the absolute risk reduction for dutasteride was 6.0% and 3.8%, respectively. On multivariable regression analysis adjusting for covariates, dutasteride significantly reduced clinical progression of benign prostatic hyperplasia with an odds ratio of 0.47 (95% CI 0.37 to 0.59, P<0.001). Analysis of time to first event yielded a hazard ratio of 0.673 (P<0.001) for those taking dutasteride. Sexual adverse events were most common and similar to prior reports.
Further prospective studies may be warranted to demonstrate generalisability of these results.
This study is the first to explore the benefit of treating asymptomatic or mildly symptomatic men with an enlarged prostate. Dutasteride significantly decreased the incidence of benign prostatic hyperplasia clinical progression.
评估度他雄胺在预防前列腺体积较大且基线国际前列腺症状评分(IPSS)<8 的无症状男性良性前列腺增生临床进展中的作用。
为期 4 年的双盲还原前列腺癌事件的度他雄胺研究(REDUCE)事后分析
1617 名随机分配至度他雄胺或安慰剂的男性,前列腺体积>40ml,且基线 IPSS<8。研究入组时排除了正在服用治疗良性前列腺增生药物的患者。
安慰剂或度他雄胺 0.5mg 每日一次。
4 年时良性前列腺增生临床进展的风险比较(定义为 IPSS 恶化≥4 分、急性尿潴留、尿路感染或与良性前列腺增生相关的手术)。
825 名参与者服用安慰剂,792 名参与者服用度他雄胺。共有 464 名(29%)发生了良性前列腺增生的临床进展,其中服用安慰剂的 297 名(36%),服用度他雄胺的 167 名(21%)(P<0.001)。相对风险降低 41%,绝对风险降低 15%,治疗需要数(NNT)为 7。在发生急性尿潴留和与良性前列腺增生相关的手术的男性中,度他雄胺的绝对风险降低分别为 6.0%和 3.8%。多变量回归分析调整协变量后,度他雄胺显著降低了良性前列腺增生的临床进展,比值比为 0.47(95%CI 0.37 至 0.59,P<0.001)。首次事件时间的分析得出,服用度他雄胺的患者发生风险比为 0.673(P<0.001)。性不良事件最为常见,与既往报告相似。
可能需要进一步的前瞻性研究来证明这些结果的普遍性。
本研究首次探讨了治疗前列腺体积较大或轻度症状的无症状男性的益处。度他雄胺显著降低了良性前列腺增生临床进展的发生率。