Jakobsen Niels Asger, Hamdy Freddie Charles, Bryant Richard John
Stoke Mandeville Hospital, UK.
Nuffield Department of Surgical Sciences, University of Oxford, UK.
J Clin Urol. 2016 Dec;9(2 Suppl):3-10. doi: 10.1177/2051415816656121. Epub 2016 Dec 1.
Prostate-specific antigen (PSA) is widely used as a biomarker in the detection of prostate cancer and for decision making regarding treatment options, response to therapy, and clinical follow-up. Despite its widespread use, it is well recognised that PSA has suboptimal performance as a screening tool due to poor specificity, resulting in high negative biopsy rates and potential 'over-diagnosis' and 'over-treatment' of clinically insignificant cancers. In particular, PSA does not reliably distinguish either cancer from benign prostatic conditions, or 'clinically significant' from 'indolent cancers', and it is inaccurate in predicting disease burden and response to treatment. There is an urgent demand for novel biomarkers to address these clinical needs. This article provides an update on the novel candidate biomarkers in development, which have shown potential for improving the detection of clinically significant cases of this malignancy.
前列腺特异性抗原(PSA)被广泛用作前列腺癌检测中的生物标志物,并用于有关治疗方案、治疗反应和临床随访的决策。尽管其应用广泛,但众所周知,由于特异性较差,PSA作为一种筛查工具的性能并不理想,导致高阴性活检率以及对临床意义不大的癌症可能进行“过度诊断”和“过度治疗”。特别是,PSA不能可靠地区分癌症与良性前列腺疾病,也不能区分“临床显著”癌症与“惰性癌症”,并且在预测疾病负担和治疗反应方面不准确。迫切需要新的生物标志物来满足这些临床需求。本文提供了正在开发的新型候选生物标志物的最新情况,这些生物标志物已显示出改善这种恶性肿瘤临床显著病例检测的潜力。