Dana-Farber Cancer Institute and Institute of Technology Assessment, Massachusetts General Hospital, Harvard Medical School, Boston, Massachusetts.
Division of General Internal Medicine, Massachusetts General Hospital, Harvard Medical School, Boston, Massachusetts.
JAMA. 2014 Mar 19;311(11):1143-9. doi: 10.1001/jama.2014.2085.
Prostate cancer screening with the prostate-specific antigen (PSA) test remains controversial.
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.
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.
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).
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.
目前,前列腺癌特异性抗原(PSA)检测筛查前列腺癌的方法仍存在争议。
通过对随机试验和相关建模研究的证据进行回顾,来检验 PSA 筛查与非筛查对前列腺癌特异性死亡率的影响,并提出一种平衡潜在获益和危害的方法。
从 2010 年 1 月 1 日至 2013 年 4 月 3 日,通过 MEDLINE、EMBASE 和 Cochrane 对照试验登记库,检索 PSA 筛查试验,以更新之前的系统评价。另在 EMBASE 和 MEDLINE 中进行检索,以确定延长已确定的 2 项大型随机试验结果的建模研究。采用美国心脏协会证据评分系统来评价证据等级。
Prostate, Lung, Colorectal and Ovarian(PLCO)screening trial 和 European Randomized Study of Screening for Prostate Cancer(ERSPC)这两项试验是 PSA 筛查的主要依据。前者表明筛查组的癌症发病率增加(相对风险[RR],1.12;95%CI,1.07-1.17),但在 13 年的随访中,PSA 筛查并未带来癌症特异性死亡率的降低(RR,1.09;95%CI,0.87-1.36)。ERSPC 表明筛查增加了癌症的发病率(RR,1.63;95%CI,1.57-1.69),并且在 11 年后改善了前列腺癌特异性死亡的风险(RR,0.79;95%CI,0.68-0.91)。ERSPC 证实,在 55 至 69 岁的男性中,PSA 筛查后每减少 1 例前列腺癌死亡,就需要额外诊断出 37 例前列腺癌(在降低前列腺癌死亡率方面,为 B 级证据)。筛查相关的危害包括假阳性结果和活检及治疗的并发症。建模研究表明,随着随访时间的延长,这种通过筛查诊断出的男性数量与预防的前列腺癌死亡人数的比例将会降低(B 级证据)。
目前的证据支持医生与 55 至 69 岁的一般风险男性讨论 PSA 筛查的利弊。只有明确表示倾向于筛查的男性才应该进行 PSA 检测。减轻筛查潜在危害的其他策略包括考虑每两年筛查一次、提高活检的 PSA 阈值、以及对新诊断为前列腺癌的男性进行保守治疗。