Department of Urology, Erasmus University Medical Center, Rotterdam, The Netherlands.
BJU Int. 2012 Dec;110(11):1654-60. doi: 10.1111/j.1464-410X.2012.11481.x. Epub 2012 Oct 8.
Study Type--Diagnosis (validating cohort) Level of Evidence 1b. What's known on the subject? and What does the study add? The European Randomized study of Screening for Prostate Cancer (ERSPC) showed a reduction in prostate cancer mortality of 21% for PSA-based screening at a median follow-up of 11 years. In the ERSPC, men are screened at 4-year intervals. A prostate biopsy is recommended for men with a PSA level ≥ 3.0 ng/mL. The study shows that the positive predictive value (PPV) of a prostate biopsy indicated by PSA-based screening remains equal throughout consecutive screening rounds in men without a previous biopsy. In men who have previously had a benign biopsy, the PPV drops considerably, but 20% of the cancers detected still show aggressive characteristics.
• To assess the positive predictive value (PPV) of prostate biopsy, indicated by a prostate-specific antigen (PSA) threshold of ≥ 3.0 ng/mL, over time, in the Rotterdam section of the European Randomized study of Screening for Prostate Cancer (ERSPC).
• In the Rotterdam section of the ERSPC, a total of 42,376 participants, aged 55-74 years, identified from population registries were randomly assigned to a screening or control arm. • For the ERSPC men undergo PSA screening at 4-year intervals. A total of three screening rounds were evaluated; therefore, only men aged 55-69 years at the first screening were eligible for the present study.
• PPVs for men without previous biopsy remained equal throughout the three subsequent screenings (25.5, 22.3 and 24.8% respectively). • Conversely, PPVs for men with a previous negative biopsy dropped significantly (12.0 and 15.2% at the second and third screening, respectively). • Additionally, in men with and without previous biopsy, the percentage of aggressive prostate cancers (clinical stage >T2b, Gleason score ≥ 7) decreased after the first round of screening from 44.4 to 23.8% in the second (P < 0.001) and 18.6% in the third round (P < 0.001). • Repeat biopsies accounted for 24.6% of all biopsies, but yielded only 8.6% of all aggressive cancers.
• In consecutive screening rounds the PPV of PSA-based screening remains equal in previously unbiopsied men. • In men with a previous negative biopsy the PPV drops considerably, but 20% of cancers detected still show aggressive characteristics. • Individualized screening algorithms should incorporate previous biopsy status in the decision to perform a repeat biopsy with the aim of further reducing unnecessary biopsies.
评估基于前列腺特异性抗原(PSA)阈值≥3.0ng/ml 的前列腺活检的阳性预测值(PPV)随时间的变化,在欧洲前列腺癌筛查随机研究(ERSPC)的鹿特丹部分。
在 ERSPC 的鹿特丹部分,共有 42376 名参与者,年龄在 55-74 岁之间,从人口登记处随机分配到筛查或对照组。对于 ERSPC 男性,每 4 年进行一次 PSA 筛查。总共评估了三个筛查轮次;因此,只有在第一次筛查时年龄在 55-69 岁的男性才有资格参加本研究。
无先前活检史的男性的 PPV 在随后的三次筛查中保持相等(分别为 25.5%、22.3%和 24.8%)。相反,有先前阴性活检史的男性的 PPV 显著下降(第二次和第三次筛查分别为 12.0%和 15.2%)。此外,在有和没有先前活检史的男性中,在前一轮筛查后,侵袭性前列腺癌(临床分期>T2b、Gleason 评分≥7)的百分比从第二次筛查的 44.4%降至 23.8%(P<0.001),在第三次筛查中降至 18.6%(P<0.001)。重复活检占所有活检的 24.6%,但仅占所有侵袭性癌症的 8.6%。
在连续的筛查轮次中,在未进行过活检的男性中,基于 PSA 的筛查的 PPV 保持不变。在有先前阴性活检史的男性中,PPV 显著下降,但检测到的 20%的癌症仍具有侵袭性特征。个体化的筛查算法应将先前的活检情况纳入决定进行重复活检的因素中,以进一步减少不必要的活检。