Vlaeminck-Guillem Virginie, Campos-Fernandes Jean-Louis, Champetier Denis, Chikh Karim, Decaussin-Petrucci Myriam, Devonec Marian, Gobeaux Nicolas, Paparel Philippe, Perrin Paul, Rodriguez-Lafrasse Claire, Ruffion Alain
Unité médicale d'oncologie et transfert, Service de biochimie et biologie moléculaire Sud, Centre hospitalier Lyon Sud, Pierre.
Ann Biol Clin (Paris). 2011 Jan-Feb;69(1):31-9. doi: 10.1684/abc.2010.0513.
The poor specificity of diagnostic strategy for prostate cancer (digital rectal examination and seric PSA) induces both a great number of useless prostate biopsies and diagnosis of non evolutive cancers. A urinary test (Progensa PCA3(®), Gen-Probe) measuring the expression of PCA3, a prostate cancer-specific gene, has recently be proposed to indicate re-biopsy. The aim of this prospective study was to evaluate diagnostic value of urinary PCA3 test for prostate cancer. In the urines of 245 patients submitted to prostate biopsy, expression of the PCA3 gene was measured and reported to that of PSA to calculate PCA3 score using a method amplifying and detecting RNA. Patients with informative samples (98%) were classified depending of the presence (n = 126) or absence (n = 114) of cancer tissue on biopsies. The median PCA3 score was significantly higher in the group with positive biopsies (p < 0.0001). Area under ROC curve was 0.70 for PCA3 as compared to that of PSA (0.53) and free/total PSA ratio (0.65). At the best threshold of 38, PCA3 test had a 59%-sensitivity and a 72%-specificity, as compared to 66% and 32% for total PSA (threshold 4 ng/mL) and 81% and 28% for free/total PSA ratio (threshold 25%). These performances were maintained in patients with seric PSA within the grey zone (4-10 ng/mL) and those with previous prostate biopsies. This study confirms the clinical value of PCA3 urinary test in helping decision for biopsies in patients with suspected prostate cancer.
前列腺癌诊断策略(直肠指检和血清前列腺特异抗原)特异性欠佳,导致大量不必要的前列腺活检以及对惰性癌的诊断。最近有人提出通过一项尿液检测(Progensa PCA3(®),基因探针公司)来检测前列腺癌特异性基因PCA3的表达,以指导再次活检。这项前瞻性研究旨在评估尿液PCA3检测对前列腺癌的诊断价值。对245例接受前列腺活检患者的尿液进行检测,采用一种扩增和检测RNA的方法测量PCA3基因的表达,并将其与PSA的表达进行比较,以计算PCA3评分。根据活检时是否存在癌组织(n = 126)或不存在癌组织(n = 114),将有可用样本的患者(98%)进行分类。活检阳性组的PCA3评分中位数显著更高(p < 0.0001)。与PSA(0.53)和游离/总PSA比值(0.65)相比,PCA3的ROC曲线下面积为0.70。在最佳阈值38时,PCA3检测的敏感性为59%,特异性为72%,而总PSA(阈值4 ng/mL)的敏感性和特异性分别为66%和32%,游离/总PSA比值(阈值25%)的敏感性和特异性分别为81%和28%。在血清PSA处于灰区(4 - 10 ng/mL)的患者以及既往接受过前列腺活检的患者中,这些性能得以维持。本研究证实了PCA3尿液检测在帮助疑似前列腺癌患者进行活检决策方面的临床价值。