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uPM3, a new molecular urine test for the detection of prostate cancer.

机译:uPM3,一种用于检测前列腺癌的新型分子尿液检测。

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OBJECTIVES: To evaluate, in a multicenter study, the diagnostic performance of a new molecular test uPM3 for detecting prostate cancer cells in urine because of the need for better methods to identify patients at risk of prostate cancer. METHODS: The uPM3 test is a nucleic acid amplification assay detecting simultaneously in the urine the relative expression of prostate-specific antigen (PSA) mRNA as a marker of prostate cells and PCA3RNA, which is selectively expressed in most types of prostate cancer. The test is performed using the isothermic nucleic acid-based amplification method, and the two targets are simultaneously detected in real-time fluorescence using specific beacons as probes in a thermostated spectrofluorometer. The test was performed on the first voided urine obtained after careful digital rectal examination of the prostate in men undergoing transrectal ultrasound-guided prostate biopsy. RESULTS: Of 517 patients undergoing biopsy at five centers, 443 (86%) had an assessable sample. Of those, 21%, 55%, and 24% had a total PSA level of less than 4 ng/mL, between 4 and 10 ng/mL, and greater than 10 ng/mL. The corresponding percentage of biopsies positive for cancer in these three groups was 20%, 35%, and 44%. The overall uPM3 sensitivity and specificity was 66% and 89%, respectively. In men with a PSA level less than 4 ng/mL, the sensitivity was 74% and specificity 91%. In those with a PSA level of 4 to 10 ng/mL, the sensitivity was 58% and specificity 91%. In those with a PSA level greater than 10 ng/mL, the sensitivity and specificity was 79% and 80%, respectively. The positive predictive value of uPM3 was 75% compared with 38% for total PSA, and the negative predictive value was 84% compared with 89% and 80% for a PSA cutoff of 2.5 and 4.0 ng/mL, respectively. The overall accuracy was 81% compared with 43% and 47% for total PSA at a cutoff of 2.5 and 4.0 ng/mL, respectively. CONCLUSIONS: These results suggest that the uPM3 molecular urine test may be an important adjunct to current methodsfor the detection of early prostate cancer.
机译:目的:在多中心研究中,评估新分子检测uPM3对尿液中前列腺癌细胞的诊断性能,因为需要更好的方法来识别有前列腺癌风险的患者。方法:uPM3测试是一种核酸扩增测定法,可同时检测尿液中前列腺特异性抗原(PSA)mRNA作为前列腺细胞和PCA3RNA的标志物的相对表达,该表达在大多数类型的前列腺癌中选择性表达。使用基于等温核酸的扩增方法进行测试,并使用特定信标作为恒温分光荧光计中的探针,同时实时荧光检测两个目标。该测试是对接受经直肠超声引导的前列腺活检的男性进行仔细的直肠直肠指检后获得的第一个排尿。结果:在五个中心的517例活检患者中,有443例(86%)具有可评估的样本。其中,分别有21%,55%和24%的总PSA含量低于4 ng / mL,介于4至10 ng / mL之间,且高于10 ng / mL。这三组中癌症活检的相应百分比分别为20%,35%和44%。 uPM3的总体敏感性和特异性分别为66%和89%。 PSA水平低于4 ng / mL的男性中,敏感性为74%,特异性为91%。 PSA水平为4至10 ng / mL的患者,敏感性为58%,特异性为91%。 PSA水平大于10 ng / mL的患者,其敏感性和特异性分别为79%和80%。 uPS3的阳性预测值为75%,而总PSA为38%,阴性预测值为84%,而PSA临界值为2.5和4.0 ng / mL则分别为89%和80%。总体准确度为81%,而总PSA的截断率为2.5和4.0 ng / mL时分别为43%和47%。结论:这些结果表明,uPM3分子尿液检测可能是当前检测早期前列腺癌方法的重要辅助手段。

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