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度他雄胺对良性前列腺增生或前列腺癌男性患者前列腺内雄激素水平的影响。

Effect of dutasteride on intraprostatic androgen levels in men with benign prostatic hyperplasia or prostate cancer.

作者信息

Rittmaster Roger, Hahn Robert G, Ray Paul, Shannon Jennifer B, Wurzel Rafael

机构信息

Urology Clinical Development and Medical Affairs, GlaxoSmithKline, Research Triangle Park, North Carolina 27709, USA.

出版信息

Urology. 2008 Oct;72(4):808-12. doi: 10.1016/j.urology.2008.06.032. Epub 2008 Aug 21.

Abstract

OBJECTIVES

Dutasteride exerts its beneficial effects on the prostate through suppression of intraprostatic dihydrotestosterone (DHT). The aim of this analysis was to assess the effects of the approved dose of dutasteride (0.5 mg/d), given for 2 weeks to 4 months, on the serum and intraprostatic DHT and testosterone levels in 3 randomized studies.

METHODS

Intraprostatic androgen levels were measured in benign prostatic tissue collected during transurethral resection of the prostate (benign prostatic hyperplasia studies, n = 256) or radical prostatectomy (prostate cancer study, n = 51), performed after 2 weeks, or 1, 3, or 4 months of treatment with dutasteride or with placebo or surgery alone. The serum androgen levels were assessed at the same points during treatment. Data from the control groups were pooled to provide 1 comparison group.

RESULTS

Dutasteride reduced the intraprostatic DHT levels by 83%, 90%, 92%, and 93% after 2 weeks and 1, 3, and 4 months of treatment, respectively, compared with placebo/surgery alone. Dutasteride reduced the serum DHT levels from baseline by 84% at 2 weeks and by approximately 90% at 1, 2, 3, and 4 months compared with a 5.2% increase in the control group. The decrease in DHT levels with dutasteride was accompanied by a reciprocal increase in the serum and intraprostatic testosterone levels. However, the intraprostatic testosterone levels in the dutasteride groups generally remained lower than the intraprostatic DHT levels in the control group.

CONCLUSIONS

The results of our study have shown that dutasteride provides near-maximal suppression of both serum and intraprostatic DHT levels in men with benign prostatic hyperplasia or prostate cancer at all points assessed.

摘要

目的

度他雄胺通过抑制前列腺内双氢睾酮(DHT)对前列腺发挥有益作用。本分析的目的是在3项随机研究中评估批准剂量的度他雄胺(0.5mg/d)服用2周 至4个月对血清和前列腺内DHT及睾酮水平的影响。

方法

在经尿道前列腺切除术(良性前列腺增生研究,n = 256)或根治性前列腺切除术(前列腺癌研究,n = 51)过程中收集良性前列腺组织,分别于度他雄胺或安慰剂治疗或单纯手术治疗2周、1、3或4个月后测量前列腺内雄激素水平。在治疗期间的相同时间点评估血清雄激素水平。将对照组数据合并以提供1个比较组。

结果

与单独使用安慰剂/手术相比,度他雄胺治疗2周、1、3和4个月后,前列腺内DHT水平分别降低了83%、90%、92%和93%。与对照组增加5.2%相比,度他雄胺使血清DHT水平在2周时从基线降低了84%,在1、2、3和4个月时降低了约90%。度他雄胺使DHT水平降低的同时,血清和前列腺内睾酮水平相应升高。然而,度他雄胺组的前列腺内睾酮水平通常仍低于对照组的前列腺内DHT水平。

结论

我们的研究结果表明,在所有评估时间点,度他雄胺对良性前列腺增生或前列腺癌男性的血清和前列腺内DHT水平均提供了近乎最大程度的抑制。

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