mosaiques diagnostics GmbH, Germany.
Int J Urol. 2012 Feb;19(2):118-25. doi: 10.1111/j.1442-2042.2011.02901.x. Epub 2011 Nov 22.
Capillary electrophoresis mass spectrometry urinary proteome analysis for prostate cancer has been shown to be highly accurate in the detection of prostate cancer. The aim of the present study was to report our experience with routine application of this test in clinical practice and its cost-effectiveness.
The urinary proteome analysis for prostate cancer test was carried out in 211 patients in outpatient centers. In 184 of them, data about their follow up and the test results were available for analysis. Prostate cancer was detected in 49 cases.
The test correctly recognized 42 out of 49 tumor patients, showing a sensitivity of 86% (95% confidence interval 73-94). Of 135 prostate cancer-negative patients, 79 had a negative urinary proteome analysis for prostate cancer test (specificity 59% [79/135 95% confidence interval 50-66]). Negative and positive predictive values were 92% (95% confidence interval 84-96) and 43% (95% confidence interval 33-53), respectively. A statistically significant (P<0.0005) improvement in terms of diagnostic accuracy was observed in comparison with serum prostate-specific antigen and percent-free prostate-specific antigen. Whereas the urinary proteome analysis for prostate cancer test results agreed in 65.7% with follow-up reference results, prostate-specific antigen achieved 33.3% and percent-free prostate-specific antigen achieved 42.7%. Cost-effectiveness analysis showed that the urinary proteome analysis for prostate cancer strategy outperformed the biopsy approach as well as prostate-specific antigen tests.
The non-invasive urinary proteome analysis for prostate cancer test appears to be a helpful addition to prostate cancer diagnostics for patients with suspicious prostate-specific antigen and/or digital-rectal examination.
毛细管电泳-质谱法尿液蛋白质组分析已被证明在前列腺癌的检测中具有高度准确性。本研究旨在报告我们在临床实践中常规应用该检测的经验及其成本效益。
在门诊中心对 211 例患者进行了前列腺癌尿液蛋白质组分析检测。在其中 184 例患者中,获得了他们的随访数据和检测结果进行分析。共检测出 49 例前列腺癌。
该检测正确识别了 49 例肿瘤患者中的 42 例,敏感性为 86%(95%置信区间 73-94)。在 135 例前列腺癌阴性患者中,79 例尿液蛋白质组分析检测为阴性(特异性 59%[79/135 95%置信区间 50-66])。阴性和阳性预测值分别为 92%(95%置信区间 84-96)和 43%(95%置信区间 33-53)。与血清前列腺特异性抗原和游离前列腺特异性抗原百分比相比,诊断准确性有统计学显著提高(P<0.0005)。虽然尿液蛋白质组分析检测结果与随访参考结果的一致性为 65.7%,但前列腺特异性抗原为 33.3%,游离前列腺特异性抗原为 42.7%。成本效益分析表明,与活检和前列腺特异性抗原检测相比,非侵入性的尿液蛋白质组分析检测策略具有优势。
对于前列腺特异性抗原和/或直肠指检可疑的前列腺癌患者,非侵入性的尿液蛋白质组分析检测似乎是一种有用的前列腺癌诊断方法。