Imperial Prostate, Division of Surgery, Department of Surgery and Cancer, Faculty of Medicine, Imperial College London, London, United Kingdom.
Department of Urology, Imperial College Healthcare National Health Service (NHS) Trust, London, United Kingdom.
JAMA Oncol. 2021 Mar 1;7(3):395-402. doi: 10.1001/jamaoncol.2020.7456.
Screening for prostate cancer using prostate-specific antigen (PSA) testing can lead to problems of underdiagnosis and overdiagnosis. Short, noncontrast magnetic resonance imaging (MRI) or transrectal ultrasonography might overcome these limitations.
To compare the performance of PSA testing, MRI, and ultrasonography as screening tests for prostate cancer.
DESIGN, SETTING, AND PARTICIPANTS: This prospective, population-based, blinded cohort study was conducted at 7 primary care practices and 2 imaging centers in the United Kingdom. Men 50 to 69 years of age were invited for prostate cancer screening from October 10, 2018, to May 15, 2019.
All participants underwent screening with a PSA test, MRI (T2 weighted and diffusion), and ultrasonography (B-mode and shear wave elastography). The tests were independently interpreted without knowledge of other results. Both imaging tests were reported on a validated 5-point scale of suspicion. If any test result was positive, a systematic 12-core biopsy was performed. Additional image fusion-targeted biopsies were performed if the MRI or ultrasonography results were positive.
The main outcome was the proportion of men with positive MRI or ultrasonography (defined as a score of 3-5 or 4-5) or PSA test (defined as PSA ≥3 μg/L) results. Key secondary outcomes were the number of clinically significant and clinically insignificant cancers detected if each test was used exclusively. Clinically significant cancer was defined as any Gleason score of 3+4 or higher.
A total of 2034 men were invited to participate; of 411 who attended screening, 408 consented to receive all screening tests. The proportion with positive MRI results (score, 3-5) was higher than the proportion with positive PSA test results (72 [17.7%; 95% CI, 14.3%-21.8%] vs 40 [9.9%; 95% CI, 7.3%-13.2%]; P < .001). The proportion with positive ultrasonography results (score, 3-5) was also higher than the proportion of those with positive PSA test results (96 [23.7%; 95% CI, 19.8%-28.1%]; P < .001). For an imaging threshold of score 4 to 5, the proportion with positive MRI results was similar to the proportion with positive PSA test results (43 [10.6%; 95% CI, 7.9%-14.0%]; P = .71), as was the proportion with positive ultrasonography results (52 [12.8%; 95% CI, 9.9%-16.5%]; P = .15). The PSA test (≥3 ng/mL) detected 7 clinically significant cancers, an MRI score of 3 to 5 detected 14 cancers, an MRI score of 4 to 5 detected 11 cancers, an ultrasonography score of 3 to 5 detected 9 cancer, and an ultrasonography score of 4 to 5 detected 4 cancers. Clinically insignificant cancers were diagnosed by PSA testing in 6 cases, by an MRI score of 3 to 5 in 7 cases, an MRI score of 4 to 5 in 5 cases, an ultrasonography score of 3 to 5 in 13 cases, and an ultrasonography score of 4 to 5 in 7 cases.
In this cohort study, when screening the general population for prostate cancer, MRI using a score of 4 or 5 to define a positive test result compared with PSA alone at 3 ng/mL or higher was associated with more men diagnosed with clinically significant cancer, without an increase in the number of men advised to undergo biopsy or overdiagnosed with clinically insignificant cancer. There was no evidence that ultrasonography would have better performance compared with PSA testing alone.
使用前列腺特异性抗原(PSA)检测进行前列腺癌筛查可能会导致漏诊和过度诊断的问题。短期、非对比磁共振成像(MRI)或经直肠超声检查可能会克服这些局限性。
比较 PSA 检测、MRI 和超声检查作为前列腺癌筛查试验的性能。
设计、地点和参与者:这是一项前瞻性、基于人群的、盲法队列研究,在英国的 7 家初级保健诊所和 2 家影像中心进行。邀请 50 至 69 岁的男性从 2018 年 10 月 10 日至 2019 年 5 月 15 日进行前列腺癌筛查。
所有参与者均接受 PSA 检测、MRI(T2 加权和弥散)和超声(B 型和剪切波弹性成像)筛查。这些测试是独立进行的,彼此之间没有任何结果的知识。两种影像学检查均根据验证后的 5 分可疑程度评分进行报告。如果任何测试结果为阳性,则进行系统的 12 核活检。如果 MRI 或超声检查结果为阳性,则进行额外的图像融合靶向活检。
主要结果是 MRI 或超声检查阳性(定义为评分 3-5 或 4-5)或 PSA 检测阳性(定义为 PSA≥3μg/L)的男性比例。关键次要结果是如果仅使用每种测试,检测到的临床显著和临床非显著癌症的数量。临床显著癌症定义为任何 Gleason 评分 3+4 或更高。
共邀请 2034 名男性参加;411 名参加筛查的男性中有 41 名参加,其中 408 名同意接受所有筛查测试。MRI 结果阳性(评分 3-5)的比例高于 PSA 检测阳性的比例(72 [17.7%;95%CI,14.3%-21.8%] 比 40 [9.9%;95%CI,7.3%-13.2%];P<0.001)。超声检查阳性(评分 3-5)的比例也高于 PSA 检测阳性的比例(96 [23.7%;95%CI,19.8%-28.1%];P<0.001)。对于影像学阈值为评分 4-5,MRI 结果阳性的比例与 PSA 检测阳性的比例相似(43 [10.6%;95%CI,7.9%-14.0%];P=0.71),超声检查阳性的比例也相似(52 [12.8%;95%CI,9.9%-16.5%];P=0.15)。PSA 检测(≥3ng/mL)检测到 7 例临床显著癌症,MRI 评分 3-5 检测到 14 例癌症,MRI 评分 4-5 检测到 11 例癌症,超声评分 3-5 检测到 9 例癌症,超声评分 4-5 检测到 4 例癌症。PSA 检测在 6 例中诊断出临床意义不显著的癌症,MRI 评分 3-5 在 7 例中诊断出临床意义不显著的癌症,MRI 评分 4-5 在 5 例中诊断出临床意义不显著的癌症,超声评分 3-5 在 13 例中诊断出临床意义不显著的癌症,超声评分 4-5 在 7 例中诊断出临床意义不显著的癌症。
在这项队列研究中,当对一般人群进行前列腺癌筛查时,与 PSA 单独检测 3ng/mL 或更高相比,MRI 采用评分 4 或 5 来定义阳性检测结果与更多诊断出具有临床意义的癌症相关,而不会增加建议进行活检的男性数量或过度诊断出具有临床意义的癌症。没有证据表明超声检查的性能会优于 PSA 单独检测。