Urologic Oncology Branch, National Cancer Institute, National Institutes of Health, Bethesda, Maryland7Dr Siddiqui is now with the Department of Surgery, Division of Urology, University of Maryland, Baltimore.
Urologic Oncology Branch, National Cancer Institute, National Institutes of Health, Bethesda, Maryland8Dr Rais-Bahrami is now with the Departments of Urology and Radiology, University of Alabama at Birmingham.
JAMA. 2015 Jan 27;313(4):390-7. doi: 10.1001/jama.2014.17942.
Targeted magnetic resonance (MR)/ultrasound fusion prostate biopsy has been shown to detect prostate cancer. The implications of targeted biopsy alone vs standard extended-sextant biopsy or the 2 modalities combined are not well understood.
To assess targeted vs standard biopsy and the 2 approaches combined for the diagnosis of intermediate- to high-risk prostate cancer.
DESIGN, SETTING, AND PARTICIPANTS: Prospective cohort study of 1003 men undergoing both targeted and standard biopsy concurrently from 2007 through 2014 at the National Cancer Institute in the United States. Patients were referred for elevated level of prostate-specific antigen (PSA) or abnormal digital rectal examination results, often with prior negative biopsy results. Risk categorization was compared among targeted and standard biopsy and, when available, whole-gland pathology after prostatectomy as the "gold standard."
Patients underwent multiparametric prostate magnetic resonance imaging to identify regions of prostate cancer suspicion followed by targeted MR/ultrasound fusion biopsy and concurrent standard biopsy.
The primary objective was to compare targeted and standard biopsy approaches for detection of high-risk prostate cancer (Gleason score ≥ 4 + 3); secondary end points focused on detection of low-risk prostate cancer (Gleason score 3 + 3 or low-volume 3 + 4) and the biopsy ability to predict whole-gland pathology at prostatectomy.
Targeted MR/ultrasound fusion biopsy diagnosed 461 prostate cancer cases, and standard biopsy diagnosed 469 cases. There was exact agreement between targeted and standard biopsy in 690 men (69%) undergoing biopsy. Targeted biopsy diagnosed 30% more high-risk cancers vs standard biopsy (173 vs 122 cases, P < .001) and 17% fewer low-risk cancers (213 vs 258 cases, P < .001). When standard biopsy cores were combined with the targeted approach, an additional 103 cases (22%) of mostly low-risk prostate cancer were diagnosed (83% low risk, 12% intermediate risk, and 5% high risk). The predictive ability of targeted biopsy for differentiating low-risk from intermediate- and high-risk disease in 170 men with whole-gland pathology after prostatectomy was greater than that of standard biopsy or the 2 approaches combined (area under the curve, 0.73, 0.59, and 0.67, respectively; P < .05 for all comparisons).
Among men undergoing biopsy for suspected prostate cancer, targeted MR/ultrasound fusion biopsy, compared with standard extended-sextant ultrasound-guided biopsy, was associated with increased detection of high-risk prostate cancer and decreased detection of low-risk prostate cancer. Future studies will be needed to assess the ultimate clinical implications of targeted biopsy.
clinicaltrials.gov Identifier: NCT00102544.
靶向磁共振(MR)/超声融合前列腺活检已被证明可检测前列腺癌。靶向活检单独与标准扩展六分法活检或两种方法联合的意义尚不清楚。
评估靶向与标准活检以及两种方法联合在诊断中高危前列腺癌中的作用。
设计、地点和参与者:这是一项前瞻性队列研究,纳入了 2007 年至 2014 年期间在美国国家癌症研究所接受靶向和标准活检的 1003 名男性患者。这些患者因前列腺特异性抗原(PSA)水平升高或直肠指检异常而被转诊,通常之前的活检结果为阴性。对靶向和标准活检以及前列腺切除术后全腺病理(作为“金标准”)进行风险分类比较。
患者接受多参数前列腺磁共振成像以识别前列腺癌可疑区域,然后进行靶向 MR/超声融合活检和同期标准活检。
主要目标是比较靶向和标准活检方法在检测高危前列腺癌(Gleason 评分≥4+3)方面的作用;次要终点集中在检测低危前列腺癌(Gleason 评分 3+3 或低体积 3+4)以及活检预测前列腺切除术后全腺病理的能力。
靶向 MR/超声融合活检诊断出 461 例前列腺癌病例,标准活检诊断出 469 例。在接受活检的 690 名男性(69%)中,靶向和标准活检完全一致。与标准活检相比,靶向活检诊断出的高危癌症多 30%(173 例与 122 例,P<0.001),低危癌症少 17%(213 例与 258 例,P<0.001)。当将标准活检芯与靶向方法结合时,又诊断出 103 例(22%)主要为低危前列腺癌(83%低危,12%中危,5%高危)。在 170 名接受前列腺切除术后全腺病理检查的男性中,靶向活检在区分低危与中高危疾病方面的预测能力优于标准活检或两种方法联合(曲线下面积分别为 0.73、0.59 和 0.67;所有比较的 P<0.05)。
在因疑似前列腺癌而接受活检的男性中,与标准扩展六分法超声引导活检相比,靶向 MR/超声融合活检与高危前列腺癌的检出率增加和低危前列腺癌的检出率降低相关。未来需要进一步研究来评估靶向活检的最终临床意义。
clinicaltrials.gov 标识符:NCT00102544。