前列腺癌症筛查:证据、正在进行的试验、政策和知识差距

O. Bratt, Anssi Auvinen, R. Arnsrud Godtman, M. Hellström, J. Hugosson, H. Lilja, J. Wallström, M. Roobol
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引用次数: 3

摘要

长期的血清前列腺特异性抗原(PSA)筛查和系统的前列腺活检可以降低前列腺癌的死亡率,但会导致不可接受的过度诊断。在过去的十年里,诊断方法得到了改进,低级别前列腺癌的惰性性质已经确立。这些进步现在使得对潜在致命性前列腺癌的检测更具选择性。这篇非系统的综述总结了相关的诊断进展、以前和正在进行的筛查试验、医疗保健政策和重要的剩余知识差距。证据综合和结论:低血清PSA值与前列腺癌死亡的最小长期风险之间的强烈关联允许调整筛查间隔。使用风险计算器、生物标志物和MRI选择PSA值升高的男性进行活检和病灶定位,而不是系统的前列腺活检,减少了低级别癌症的检测,从而导致过度诊断。这些改进最近促使欧盟建议其成员国评估有组织的前列腺癌筛查项目的可行性和有效性。尽管如此,重要的知识差距仍然存在,例如现代诊断方法在长期筛查规划中的表现及其对死亡率的影响。目前,三个大型随机筛选试验正在解决知识差距问题。以人口为基础的试点方案将提供重要的实际经验。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Screening for prostate cancer: evidence, ongoing trials, policies and knowledge gaps
Long-term screening with serum prostate-specific antigen (PSA) and systematic prostate biopsies can reduce prostate cancer mortality but leads to unacceptable overdiagnosis. Over the past decade, diagnostic methods have improved and the indolent nature of low-grade prostate cancer has been established. These advances now enable more selective detection of potentially lethal prostate cancer. This non-systematic review summarises relevant diagnostic advances, previous and ongoing screening trials, healthcare policies and important remaining knowledge gaps.Evidence synthesis and conclusions: The strong association between low serum PSA values and minimal long-term risk of prostate cancer death allows for adjusting screening intervals. Use of risk calculators, biomarkers and MRI to select men with a raised PSA value for biopsy and lesion-targeting rather than systematic prostate biopsies reduce the detection of low-grade cancer and thereby overdiagnosis. These improvements recently led the European Union to recommend its member states to evaluate the feasibility and effectiveness of organised screening programmes for prostate cancer. Nonetheless, important knowledge gaps remain such as the performance of modern diagnostic methods in long-term screening programmes and their impact on mortality. The knowledge gaps are currently being addressed in three large randomised screening trials. Population-based pilot programmes will contribute critical practical experience.
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