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前列腺癌中的液体活检潜在生物标志物

Liquid Biopsy Potential Biomarkers in Prostate Cancer.

作者信息

Neuhaus Jochen, Yang Bo

机构信息

Department of Urology, Research Laboratory, University Leipzig, D-04103 Leipzig, Germany.

出版信息

Diagnostics (Basel). 2018 Sep 21;8(4):68. doi: 10.3390/diagnostics8040068.

Abstract

Prostate cancer (PCa) is the second most common cancer in men worldwide with an incidence of 14.8% and a mortality of 6.6%. Shortcomings in comprehensive medical check-ups in low- and middle-income countries lead to delayed detection of PCa and are causative of high numbers of advanced PCa cases at first diagnosis. The performance of available biomarkers is still insufficient and limited applicability, including logistical and financial burdens, impedes comprehensive implementation into health care systems. There is broad agreement on the need of new biomarkers to improve (i) early detection of PCa, (ii) risk stratification, (iii) prognosis, and (iv) treatment monitoring. This review focuses on liquid biopsy tests distinguishing high-grade significant (Gleason score (GS) ≥ 7) from low-grade indolent PCa. Available biomarkers still lack performance in risk stratification of biopsy naïve patients. However, biomarkers with highly negative predictive values may help to reduce unnecessary biopsies. Risk calculators using integrative scoring systems clearly improve decision-making for invasive prostate biopsy. Emerging biomarkers have the potential to substitute PSA and improve the overall performance of risk calculators. Until then, PSA should be used and may be replaced whenever enough evidence has accumulated for better performance of a new biomarker.

摘要

前列腺癌(PCa)是全球男性中第二常见的癌症,发病率为14.8%,死亡率为6.6%。低收入和中等收入国家综合体检的不足导致前列腺癌检测延迟,是初诊时大量晚期前列腺癌病例的原因。现有生物标志物的性能仍然不足,且适用性有限,包括后勤和经济负担,阻碍了其在医疗保健系统中的全面应用。对于新型生物标志物以改善(i)前列腺癌的早期检测、(ii)风险分层、(iii)预后和(iv)治疗监测的需求,人们已达成广泛共识。本综述重点关注区分高级别显著前列腺癌(Gleason评分(GS)≥7)与低级别惰性前列腺癌的液体活检检测。现有生物标志物在未经活检患者的风险分层方面仍缺乏性能。然而,具有高阴性预测值的生物标志物可能有助于减少不必要的活检。使用综合评分系统的风险计算器明显改善了侵袭性前列腺活检的决策。新兴生物标志物有可能替代前列腺特异性抗原(PSA)并提高风险计算器的整体性能。在此之前,应使用PSA,并且只要积累了足够的证据证明新生物标志物性能更佳,就可以将其替代。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/094b/6316409/3e94f08dde4c/diagnostics-08-00068-g001.jpg

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