前瞻性使用游离PSA避免重复前列腺活检的男性总PSA升高。

The Prostate. Supplement Pub Date : 1996-01-01
T O Morgan, D G McLeod, E S Leifer, J W Moul, G P Murphy
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引用次数: 0

摘要

背景:前列腺特异性抗原(PSA)是早期发现前列腺癌的一种最有价值的工具;然而,目前在前列腺癌筛查项目中,它有很高的假阳性率。患者持续PSA升高,直肠指检正常,多次阴性活检呈现临床困境。我们前瞻性地评估游离PSA是否能提高PSA的特异性,并可作为一种临床指导,以避免在这类患者中重复前列腺活检。方法:67例PSA持续升高的男性(平均9.6 ng/mL;范围4.1-24.8 ng/mL),正常的直肠指检,以及两次或两次以上的六分仪活检(平均2.8),收集血清用于测量总PSA和游离PSA。所有患者都进行了再活检,以确定前列腺癌检测中总PSA与游离PSA百分比的接受者操作特征(ROC)。结果:本研究通过活检鉴定了11例新发前列腺癌。无前列腺癌男性的游离PSA中位数为18.1%,显著高于前列腺癌男性的6.4% (P < 0.00005)。当灵敏度与特异性对比时,游离PSA百分比的受试者工作曲线下面积(ROC)为0.95,而游离PSA密度为0.75,PSA密度为0.59,PSA为0.54。对于总PSA水平升高、直肠指检正常、既往两组六分仪前列腺活检阴性的患者,10%游离PSA的临界值将保持91%的敏感性,相应的特异性为86%。结论:在诊断不确定的病例中,选择性测定游离PSA百分比比单独测定总PSA可显著提高前列腺癌检测的特异性。低游离PSA(< 10%)似乎是前列腺癌的重要预测因子,即使在两次或两次以上前列腺活检阴性后也是如此。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Prospective use of free PSA to avoid repeat prostate biopsies in men with elevated total PSA.

Background: Prostate-specific antigen (PSA) is a most valuable tool for the early detection of prostate cancer; however, it has a high false-positive rate as presently used in prostate cancer screening programs. Patients with persistent PSA elevations, normal digital rectal examinations, and multiple negative biopsies present a clinical dilemma. We prospectively evaluated whether free PSA improves the specificity of PSA and can be useful as a clinical guide to avoid repeat prostate biopsies in a group of such patients.

Methods: Sixty-seven men with persistent PSA elevations (mean 9.6 ng/mL; range 4.1-24.8 ng/mL), normal digital rectal examinations, and two or more prior sextant biopsies (mean 2.8), had serum collected for measurement of total and free PSA. All patients were rebiopsied to determine the receiver-operating characteristics (ROC) of total PSA vs. percent free PSA for prostate cancer detection.

Results: This study by biopsy identified 11 new prostate cancer cases. The median percent free PSA was significantly higher at 18.1% among men without prostate cancer, compared to 6.4% in men with prostate cancer (P < 0.00005). When sensitivity was plotted against I-specificity, the area under the receiver-operating curve (ROC) for percent free PSA was 0.95, compared to 0.75 for free PSA density, 0.59 for PSA density, and 0.54 for PSA. In patients with elevated total PSA levels, normal digital rectal examinations, and two prior sets of negative sextant prostate biopsies, a cutoff of 10% free PSA would maintain sensitivity at 91% with a corresponding specificity of 86%.

Conclusions: Selective measurement of percent free PSA in cases of uncertain diagnosis can significantly improve the specificity of prostate cancer detection compared to total PSA alone. A low percent free PSA (< 10%) appears to be a significant predictor of prostate cancer even after two or more negative prostate biopsies.

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