首页> 外文期刊>European urology >Effect of dutasteride on prostate biopsy rates and the diagnosis of prostate cancer in men with lower urinary tract symptoms and enlarged prostates in the Combination of Avodart and Tamsulosin trial.
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Effect of dutasteride on prostate biopsy rates and the diagnosis of prostate cancer in men with lower urinary tract symptoms and enlarged prostates in the Combination of Avodart and Tamsulosin trial.

机译:在Avodart和Tamsulosin联合试验中,度他雄胺对下尿路症状和前列腺肥大的男性的前列腺活检率和前列腺癌的诊断有影响。

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BACKGROUND: A 23% relative risk reduction (RRR) in prostate cancer (PCa) was shown in men receiving dutasteride in the 4-yr Reduction by Dutasteride of Prostate Cancer Events study, in whom biopsies were protocol dependent. OBJECTIVE: Our aim was to explore PCa risk reduction in men with benign prostatic hyperplasia (BPH) from the Combination of Avodart and Tamsulosin (CombAT) study, in which biopsies were undertaken for cause. DESIGN, SETTING, AND PARTICIPANTS: CombAT was a 4-yr randomized double-blind parallel group study in 4844 men >/=50 yr of age with clinically diagnosed moderate to severe BPH, International Prostate Symptom Score >/=12, prostate volume >/=30 ml, and serum prostate-specific antigen (PSA) 1.5-10 ng/ml. Men underwent annual PSA measurement and digital rectal examination (DRE), and prostate biopsies were performed for cause. INTERVENTION: All patients took tamsulosin 0.4 mg/d, dutasteride 0.5 mg/d, or a combination of both. MEASUREMENTS: The primary end point was incidence of PCa. Secondary end points included postbaseline prostate biopsy rates and Gleason score of cancers. RESULTS AND LIMITATIONS: Dutasteride (alone or in combination with tamsulosin) was associated with a 40% RRR of PCa diagnosis compared with tamsulosin monotherapy (95% confidence interval, 16-57%; p=0.002) and a 40% reduction in the likelihood of biopsy. There were similar reductions in low- and high-grade Gleason score cancers. The biopsy rate in the groups receiving dutasteride trended toward a higher diagnostic yield (combination: 29%, dutasteride: 28%, tamsulosin: 24%). One limitation was the lack of a standardized approach to PCa diagnosis and grading. CONCLUSIONS: Dutasteride, alone or in combination with tamsulosin, significantly reduced the relative risk of PCa diagnosis in men with BPH undergoing annual DRE and PSA screening. Consistent with the increased usefulness of PSA for PCa detection, men receiving dutasteride had a numerically lower biopsy rate and higher yield of PCa on biopsy. TRIAL REGISTRATION: Clinicaltrials.gov identifier: NCT00090103 (http://www.clinicaltrials.gov/ct2/show/NCT00090103).
机译:背景:前列腺癌事件研究中的度他雄胺降低4年研究显示,接受度他雄胺治疗的男性的前列腺癌(PCa)相对危险度降低(RRR)为23%。目的:我们的目的是通过Avodart和Tamsulosin(CombAT)研究的联合研究,探讨降低前列腺良性增生(BPH)男性PCa的风险,该研究针对原因进行了活检。设计,地点和参与者:CombAT是一项为期4年的随机双盲平行研究,研究对象为4844名年龄≥50岁的男性,临床诊断为中度至重度BPH,国际前列腺症状评分> / = 12,前列腺体积> / = 30 ml,血清前列腺特异性抗原(PSA)为1.5-10 ng / ml。男性每年进行PSA测量和直肠指检(DRE),并进行前列腺活检以确定病因。干预:所有患者均接受坦索罗辛0.4 mg / d,度他雄胺0.5 mg / d或两者合用。测量:主要终点是PCa的发生率。次要终点包括基线后前列腺活检率和癌症的格里森评分。结果与局限性:与坦索罗辛单药治疗(95%置信区间,16-57%; p = 0.002)相比,度他雄胺(单独或与坦索罗辛联用)与PCa诊断的40%的RRR有关,可能性降低40%活检。低度和高度格里森评分癌症也有类似的减少。接受度他雄胺治疗的组的活检率趋于更高的诊断率(组合:29%,度他雄胺:28%,坦洛新:24%)。一个局限是缺乏PCa诊断和分级的标准化方法。结论:度他雄胺单独或与坦洛新联合使用,可显着降低接受每年DRE和PSA筛查的BPH男性PCa诊断的相对风险。与PSA对PCa检测的有用性增加相一致,接受度他雄胺的男性在活检中的活检率在数值上较低,而PCa的产率较高。试验注册:Clinicaltrials.gov标识符:NCT00090103(http://www.clinicaltrials.gov/ct2/show/NCT00090103)。

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