首页> 外文期刊>Urology >Prostate cancer gene 3 score predicts prostate biopsy outcome in men receiving dutasteride for prevention of prostate cancer: results from the REDUCE trial.
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Prostate cancer gene 3 score predicts prostate biopsy outcome in men receiving dutasteride for prevention of prostate cancer: results from the REDUCE trial.

机译:前列腺癌基因3评分可预测接受度他雄胺预防前列腺癌的男性的前列腺活检结果:REDUCE试验的结果。

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OBJECTIVES: To examine the ability of the urinary prostate cancer gene 3 (PCA3) assay to predict biopsy-detected cancers in men receiving dutasteride in the Reduction by Dutasteride of Prostate Cancer Events (REDUCE) study cohort. METHODS: Urine and serum samples from 930 men in the active arm were acquired at years 2 and 4 of the biopsy visits. In addition to univariate logistic regression and receiver operating characteristic analysis, multivariate analysis for association with biopsy outcome was performed for PCA3 score in the presence of serum prostate-specific antigen (PSA), age, prostate volume, and family history of prostate cancer. RESULTS: At year 2, the univariate PCA3 score area under the receiver operating characteristic curve (AUC) was 0.668 versus 0.603 for PSA. At year 4, the PCA3 assay significantly predicted the biopsy outcome (AUC 0.628, 95% confidence interval 0.556-0.700), and the PSA level was not predictive (AUC 0.556, 95% confidence interval 0.469-0.642). The year 2 multivariate model yielded an AUC of 0.712. Removing the PCA3 score decreased the AUC to 0.660 (P = .0166 vs the full model). The median PCA3 scores in the dutasteride arm were not different from those in the 1072 men in the placebo arm (16.2 and 17.2 at year 2, P = .1755; and 18.8 and 18.1 at year 4, P = .2340, respectively). However, the PSA values were reduced >50% in the dutasteride arm at both visits (both P < .0001 vs placebo). At a PCA3 score cutoff of 35, the sensitivity and specificity were equivalent between the 2 arms. CONCLUSIONS: In the present study, the PCA3 assay outperformed PSA for cancer detection in men undergoing dutasteride treatment and improved the diagnostic accuracy when combined with the PSA level and other clinical variables. In addition, no adjustment in PCA3 score was needed to yield equivalent clinical performance between the dutasteride and placebo arms. These findings are particularly important in light of the potential role of dutasteride for prostate cancer chemoprevention.
机译:目的:研究尿路前列腺癌基因3(PCA3)测定法在接受经度他雄胺减少前列腺癌事件(REDUCE)研究队列的男性中经活检发现的癌症的预测能力。方法:在活检的第2年和第4年从活动臂中的930名男性中采集尿液和血清样本。除了单因素逻辑回归和接受者操作特征分析外,在存在血清前列腺特异性抗原(PSA),年龄,前列腺体积和前列腺癌家族史的情况下,对PCA3评分进行与活检结果相关的多元分析。结果:在第2年,受试者工作特征曲线(AUC)下的单变量PCA3得分区域为0.668,而PSA为0.603。在第4年,PCA3分析可显着预测活检结果(AUC 0.628,95%置信区间0.556-0.700),而PSA水平不是可预测的(AUC 0.556,95%置信区间0.469-0.642)。 2年级多元模型得出的AUC为0.712。删除PCA3分数会将AUC降低到0.660(与完整模型相比,P = .0166)。度他雄胺组的PCA3得分中位数与安慰剂组的1072名男性的PCA3得分没有差异(第二年分别为16.2和17.2,P = .1755;第四年分别为18.8和18.1,P = 0.234)。但是,在两次访问中,度他雄胺组的PSA值均降低了> 50%(相对于安慰剂,P <.0001)。在PCA3评分截止值为35时,两个组之间的敏感性和特异性是相同的。结论:在本研究中,PCA3测定法在接受度他雄胺治疗的男性中的癌症检测性能优于PSA,并且结合PSA水平和其他临床变量可以提高诊断准确性。此外,无需调整PCA3评分即可在度他雄胺和安慰剂组之间产生同等的临床表现。考虑到度他雄胺对前列腺癌化学预防的潜在作用,这些发现特别重要。

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