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首页> 外文期刊>JAMA: the Journal of the American Medical Association >Screening for prostate cancer with the prostate-specific antigen test: A review of current evidence
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Screening for prostate cancer with the prostate-specific antigen test: A review of current evidence

机译:用前列腺特异性抗原测试筛查前列腺癌:当前证据回顾

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IMPORTANCE: Prostate cancer screening with the prostate-specific antigen (PSA) test remains controversial. OBJECTIVE: To review evidence from randomized trials and related modeling studies examining the effect of PSA screening vs no screening on prostate cancer-specific mortality and to suggest an approach balancing potential benefits and harms. EVIDENCE ACQUISITION: MEDLINE, EMBASE, and the Cochrane Register of Controlled Trials were searched from January 1, 2010, to April 3, 2013, for PSA screening trials to update a previous systematic review. Another search was performed in EMBASE and MEDLINE to identify modeling studies extending the results of the 2 large randomized trials identified. The American Heart Association Evidence-Based Scoring System was used to rate level of evidence. RESULTS: Two trials - the Prostate, Lung, Colorectal and Ovarian (PLCO) screening trial and the European Randomized Study of Screening for Prostate Cancer (ERSPC) - dominate the evidence regarding PSA screening. The former trial demonstrated an increase in cancer incidence in the screening group (relative risk [RR], 1.12; 95% CI, 1.07-1.17) but no cancer-specific mortality benefit to PSA screening after 13-year follow-up (RR, 1.09; 95% CI, 0.87-1.36). The ERSPC demonstrated an increase in cancer incidence with screening (RR, 1.63; 95% CI, 1.57-1.69) and an improvement in the risk of prostate cancer-specific death after 11 years (RR, 0.79; 95% CI, 0.68-0.91). The ERSPC documented that 37 additional men needed to receive a diagnosis through screening for every 1 fewer prostate cancer death after 11 years of follow-up among men aged 55 to 69 years (level B evidence for prostate cancer mortality reduction). Harms associated with screening include false-positive results and complications of biopsy and treatment. Modeling studies suggest that this high ratio of additional men receiving diagnoses to prostate cancer deaths prevented will decrease during a longer follow-up (level B evidence). CONCLUSIONS AND RELEVANCE: Available evidence favors clinician discussion of the pros and cons of PSA screening with average-risk men aged 55 to 69 years. Only men who express a definite preference for screening should have PSA testing. Other strategies to mitigate the potential harms of screening include considering biennial screening, a higher PSA threshold for biopsy, and conservative therapy for men receiving a new diagnosis of prostate cancer.
机译:重要提示:前列腺特异性抗原(PSA)测试对前列腺癌的筛查仍存在争议。目的:回顾来自随机试验和相关模型研究的证据,这些研究检查了PSA筛查与不筛查PSA对前列腺癌特异性死亡率的影响,并提出了一种平衡潜在利弊的方法。证据获取:从2010年1月1日至2013年4月3日,检索MEDLINE,EMBASE和对照试验的Cochrane登记册,以进行PSA筛查试验,以更新先前的系统评价。在EMBASE和MEDLINE中进行了另一次搜索,以识别建模研究,从而扩展了所识别的2个大型随机试验的结果。美国心脏协会循证评分系统用于评估证据水平。结果:两项试验-前列腺癌,肺癌,结肠直肠癌和卵巢癌(PLCO)筛查试验以及欧洲前列腺癌筛查随机研究(ERSPC)-主导了PSA筛查的证据。先前的研究表明,筛查组的癌症发生率有所增加(相对危险度[RR],1.12; 95%CI,1.07-1.17),但13年随访后,没有针对PSA筛查的癌症特异性死亡率受益(RR, 1.09; 95%CI,0.87-1.36)。 ERSPC筛查显示癌症发生率增加(RR,1.63; 95%CI,1.57-1.69),11年后前列腺癌特异性死亡风险增加(RR,0.79; 95%CI,0.68-0.91) )。 ERSPC记录表明,在55至69岁的男性中,经过11年的随访,每增加1名前列腺癌死亡病例,就有37名男性需要通过筛查进行诊断(B级前列腺癌死亡率降低的证据)。与筛查相关的危害包括假阳性结果以及活检和治疗并发症。模型研究表明,接受更多诊断的男性与被预防的前列腺癌死亡的比例如此之高,将在更长的随访期间降低(B级证据)。结论和相关性:现有证据支持临床医生讨论55岁至69岁中等风险男性PSA筛查的利与弊。只有明确表示愿意接受筛查的男性才能进行PSA检测。减轻筛查潜在危害的其他策略包括考虑进行两年一次的筛查,更高的活检PSA阈值以及对接受前列腺癌新诊断的男性进行保守治疗。

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