Urology Department, Clinica Las Condes, Santiago, Chile.
Urol Oncol. 2013 Nov;31(8):1522-6. doi: 10.1016/j.urolonc.2012.05.002. Epub 2012 Jun 9.
Prostate Cancer Gene 3 (PCA3) is a recently described and highly specific urinary marker for prostate cancer (CaP). Its introduction in clinical practice to supplement low specificity of prostate specific antigen (PSA) can improve CaP diagnosis and follow-up. However, before its introduction, it is necessary to validate the method of PCA3 detection in distinct geographic populations.
Our aim was to describe for the first time in Latin America, the application of the PROGENSA PCA3 assay for PCA3 detection in urine in Chilean men and its utility for CaP diagnosis in men with an indication of prostate biopsy.
Sixty-four Chilean patients (mean age, 64 years) with indication of prostate biopsy because of elevated PSA and/or suspicious digital rectal examination (DRE) were prospectively recruited. PCA3 scores were assessed from urine samples obtained after DRE, before biopsy, and compared with PSA levels and biopsy outcome.
The median PSA value and mean PCA3 score were 5.8 ng/ml and 31.7, respectively. Using a cutoff PCA3 score of 35, the sensitivity and specificity for detecting CaP were 52% and 87%, respectively. The receiver operating characteristic (ROC) curve analysis showed an area under the curve of 0.77 for PCA3 and 0.57 for PSA, for the same group of patients. In patients with previous negative biopsy, PCA3 specificity increased by 2.2%.
This is the first report in Latin America on the use of PCA3 in diagnosing CaP. Our results are comparable to those reported in other populations in the literature, demonstrating the reproducibility of the test. PCA3 score was highly specific and we specially recommend its use in patients with persistent elevated PSA and prior negative biopsies.
前列腺癌基因 3(PCA3)是一种新描述的、高度特异的前列腺癌(CaP)尿标志物。将其引入临床实践,以补充前列腺特异性抗原(PSA)的低特异性,可以提高 CaP 的诊断和随访。然而,在引入之前,有必要验证 PCA3 在不同地理人群中的检测方法。
我们的目的是首次在拉丁美洲描述 PROGENSA PCA3 检测在智利男性尿液中 PCA3 的检测,并评估其在有前列腺活检指征的男性中对 CaP 诊断的应用。
64 名智利患者(平均年龄 64 岁)因 PSA 升高和/或直肠指诊(DRE)可疑而接受了前瞻性前列腺活检。评估 DRE 后、活检前采集的尿液标本中的 PCA3 评分,并与 PSA 水平和活检结果进行比较。
中位 PSA 值和平均 PCA3 评分分别为 5.8ng/ml 和 31.7。使用 35 的截断 PCA3 评分,检测 CaP 的敏感性和特异性分别为 52%和 87%。ROC 曲线分析显示,对于同一组患者,PCA3 的曲线下面积为 0.77,PSA 为 0.57。在以前活检阴性的患者中,PCA3 的特异性增加了 2.2%。
这是拉丁美洲首次关于 PCA3 用于诊断 CaP 的报告。我们的结果与文献中其他人群的报告相当,证明了该检测的可重复性。PCA3 评分具有高度的特异性,我们特别推荐在持续 PSA 升高和先前阴性活检的患者中使用。