PSA and the Detection of Prostate Cancer After 2005. Part I

EAU-EBU Update Series Pub Date : 2006-02-01 Epub Date: 2005-12-22 DOI:10.1016/j.eeus.2005.11.003
Fritz H. Schröder, Claartje Gosselaar, Stijn Roemeling, Renske Postma, Monique J. Roobol, Chris H. Bangma
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引用次数: 11

Abstract

PSA has been shown to be a powerful tool to detect prostate cancer in men at risk due to their age. Catalona et al. [1] used a PSA cut-off value of 4 ng/mL in a group of 1653 men in age groups at risk as a biopsy indication. 37 cancers (2.3%) were detected. 16 of the 37 cancers would have been missed by rectal examination alone. With increasing use of PSA it then emerged that the prostate cancers detected in excess of rectal examination had a more favourable distribution of prognostic factors. This was again shown early on in a prospective setting by Catalona et al. [2]. Recent developments have cast doubt on the use of the traditional PSA cut-off of 4.0 ng/mL and on the value of PSA levels in general and specifically in heavily pre-screened populations. It seems that recent findings, which will be subject to review in this paper, have made the role of PSA in diagnosing prostate cancer more uncertain than ever before. While lowering PSA cut-off levels leads to a higher detection rate of prostate cancer, it also leads to an increase of the diagnosis of cancers which might otherwise never bother their carrier (overdiagnosis). In addition, potentially aggressive cancers as defined by Gleason scores above 7 cannot be identified by appropriate PSA cut-off levels. Even with PSA values below 3.0 ng/mL 10–15% of cancers identified have been shown to have aggressive features. The high rate of overdiagnosis makes strategies desirable, which identify aggressive but still curable cancers with an acceptable accuracy. This unfortunately is still impossible. Potentially valid approaches, which include the use of PSA kinetics over time, are in the process of being evaluated. The best way of making use of PSA in the future for diagnosing prostate cancer and its role in differentiating between aggressive and less aggressive tumours seems uncertain at this time. Further research in this field is urgently needed and directions are outlined. For the time being, arbitrary cut-off levels will remain the best option even in repeat screening.

2005年后PSA与前列腺癌的检测。第一部分
PSA已被证明是检测前列腺癌的有力工具,因为他们的年龄有患前列腺癌的风险。Catalona等人[1]采用PSA临界值4 ng/mL作为活检指征,对1653名高危年龄组男性进行了研究。发现37例癌症(2.3%)。37例癌症中有16例仅通过直肠检查就会被遗漏。随着PSA使用的增加,直肠检查中发现的前列腺癌具有更有利的预后因素分布。Catalona等人[2]在早期的前瞻性设置中再次证明了这一点。最近的发展使人们对传统的PSA临界值4.0 ng/mL的使用以及PSA水平的一般价值,特别是在经过大量预先筛选的人群中的价值产生了怀疑。最近的研究结果似乎使PSA在诊断前列腺癌中的作用比以往任何时候都更加不确定,这些发现将在本文中进行综述。虽然降低PSA临界值会提高前列腺癌的检出率,但它也会增加癌症的诊断率,否则这些癌症可能不会困扰其携带者(过度诊断)。此外,Gleason评分高于7分的潜在侵袭性癌症不能通过适当的PSA临界值来识别。即使PSA值低于3.0 ng/mL, 10-15%的癌症已被证实具有侵袭性特征。高的过度诊断率使得鉴别具有侵袭性但仍可治愈的癌症的策略具有可接受的准确性。不幸的是,这仍然是不可能的。潜在的有效方法,包括随时间使用PSA动力学,正在评估过程中。在未来,利用PSA诊断前列腺癌的最佳方法及其在区分侵袭性和非侵袭性肿瘤中的作用目前似乎还不确定。这一领域亟待进一步研究,并提出了发展方向。目前,即使在重复筛查中,任意切断水平仍将是最佳选择。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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