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前列腺癌筛查

Prostate cancer screening.

作者信息

Tenke P, Horti J, Balint P, Kovacs B

机构信息

Department of Urology, Jahn Ferenc South-Pest Hospital, Budapest, Hungary.

出版信息

Recent Results Cancer Res. 2007;175:65-81. doi: 10.1007/978-3-540-40901-4_5.

Abstract

Prostate cancer incurs a substantial incidence and mortality burden, similarly to breast cancer, and it ranks among the top ten specific causes of death in the United States. It is inherent as we maximize the detection of early prostate cancer that we increase the detection of both nonaggressive (slow growing) and aggressive (faster growing) prostate cancers. The evidence clearly supports the use of PSA screening in conjunction with DRE as a means of early detection of prostate cancer. Widespread implementation of prostate cancer screening in the United States has led to the phenomenon of stage migration with more cancers being detected at a lower stage. Such a trend has decreased the incidence of metastatic disease at diagnosis and paralleled the decrease of the mortality rate from prostate cancer. Our understanding of the natural history of prostate cancer is progressing over time, but the question of its length is unanswerable. The relatively long doubling time (on average) of early prostate cancer of 3 to 4 years or more indicates a relatively good prognosis for many men with this disease, even without early detection and treatment. Unfortunately, the poor specificity of the PSA test in men with benign prostatic hyperplasia (BPH) leads to high rates of prostate biopsy and attendant illnesses and costs. Early detection is more apt to detect a slow-growing prostate cancer than a faster growing cancer that is associated with a more rapid course of progression to metastatic disease. Hence, the launching of mass screening programs for the early detection of prostate cancer is premature. However, in the absence of solid evidence of benefit, one reasonable approach to screening at the individual level is to involve the patient in decisions about whether or not to perform a PSA test. Thus, "offering" PSA testing must be accompanied by informed discussion within the context of an ongoing patient-physician relationship. This is to be distinguished from the use of PSA testing for the purpose of "mass screening." Concepts that must be explored with the patient include: 1. The long-term ramifications of screening 2. The relatively high probability of further evaluation and biopsy with positive results 3. Potentially difficult decisions that may arise about using treatments that are associated with considerable morbidity and uncertain benefits (at the time) if cancer is discovered We should identify a future path that is evidence-based, focused on the issues that make a difference to patients, and results in better and longer lives of those with the disease and those who are at risk of getting it. If that path leads to treating fewer patients in the future, even if sometimes more aggressively, we should pursue it definitely and consequently.

摘要

前列腺癌与乳腺癌一样,造成了相当大的发病和死亡负担,在美国位列十大特定死因。随着我们最大限度地检测早期前列腺癌,不可避免地会增加对非侵袭性(生长缓慢)和侵袭性(生长较快)前列腺癌的检测。有明确证据支持将前列腺特异性抗原(PSA)筛查与直肠指检(DRE)结合使用,作为早期检测前列腺癌的一种手段。在美国广泛开展前列腺癌筛查导致了分期迁移现象,更多癌症在较低分期被检测出来。这种趋势降低了诊断时转移性疾病的发病率,同时前列腺癌死亡率也随之下降。随着时间的推移,我们对前列腺癌自然史的认识不断进步,但关于其病程长短的问题仍无法回答。早期前列腺癌相对较长的平均倍增时间(3至4年或更长)表明,许多患此病的男性即使没有早期检测和治疗,预后也相对较好。不幸的是,PSA检测在良性前列腺增生(BPH)男性中的特异性较差,导致前列腺活检率较高,随之而来的是疾病和成本增加。早期检测更有可能检测出生长缓慢的前列腺癌,而不是与更快进展至转移性疾病相关的生长较快的癌症。因此,开展大规模前列腺癌早期检测筛查项目为时过早。然而,在缺乏确凿获益证据的情况下,个体层面筛查的一种合理方法是让患者参与关于是否进行PSA检测的决策。因此,“提供”PSA检测必须在持续的医患关系背景下,伴随知情讨论。这与用于“大规模筛查”目的的PSA检测有所不同。必须与患者探讨的概念包括:1. 筛查的长期影响;2. 进一步评估和活检结果为阳性的相对高概率;3. 如果发现癌症,在使用与相当大发病率和不确定获益(当时)相关的治疗方法时可能出现的潜在困难决策。我们应该确定一条基于证据的未来道路,关注对患者有影响的问题,并使患者及其有患病风险的人生活得更好、更长久。如果这条道路导致未来治疗的患者减少,即使有时治疗更积极,我们也应坚定地追求并遵循它。

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