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对先前活检结果为阴性的患者,使用磁共振和超声图像融合引导经会阴前列腺活检进行靶向和系统活检的多中心评估。

Multicentre evaluation of targeted and systematic biopsies using magnetic resonance and ultrasound image-fusion guided transperineal prostate biopsy in patients with a previous negative biopsy.

作者信息

Hansen Nienke L, Kesch Claudia, Barrett Tristan, Koo Brendan, Radtke Jan P, Bonekamp David, Schlemmer Heinz-Peter, Warren Anne Y, Wieczorek Kathrin, Hohenfellner Markus, Kastner Christof, Hadaschik Boris

机构信息

Department of Diagnostic and Interventional Radiology, University Hospital RWTH Aachen, Aachen, Germany.

CamPARI Clinic, Addenbrooke's Hospital and University of Cambridge, Cambridge, UK.

出版信息

BJU Int. 2017 Nov;120(5):631-638. doi: 10.1111/bju.13711. Epub 2016 Dec 21.

Abstract

OBJECTIVES

To evaluate the detection rates of targeted and systematic biopsies in magnetic resonance imaging (MRI) and ultrasound (US) image-fusion transperineal prostate biopsy for patients with previous benign transrectal biopsies in two high-volume centres.

PATIENTS AND METHODS

A two centre prospective outcome study of 487 patients with previous benign biopsies that underwent transperineal MRI/US fusion-guided targeted and systematic saturation biopsy from 2012 to 2015. Multiparametric MRI (mpMRI) was reported according to Prostate Imaging Reporting and Data System (PI-RADS) Version 1. Detection of Gleason score 7-10 prostate cancer on biopsy was the primary outcome. Positive (PPV) and negative (NPV) predictive values including 95% confidence intervals (95% CIs) were calculated. Detection rates of targeted and systematic biopsies were compared using McNemar's test.

RESULTS

The median (interquartile range) PSA level was 9.0 (6.7-13.4) ng/mL. PI-RADS 3-5 mpMRI lesions were reported in 343 (70%) patients and Gleason score 7-10 prostate cancer was detected in 149 (31%). The PPV (95% CI) for detecting Gleason score 7-10 prostate cancer was 0.20 (±0.07) for PI-RADS 3, 0.32 (±0.09) for PI-RADS 4, and 0.70 (±0.08) for PI-RADS 5. The NPV (95% CI) of PI-RADS 1-2 was 0.92 (±0.04) for Gleason score 7-10 and 0.99 (±0.02) for Gleason score ≥4 + 3 cancer. Systematic biopsies alone found 125/138 (91%) Gleason score 7-10 cancers. In patients with suspicious lesions (PI-RADS 4-5) on mpMRI, systematic biopsies would not have detected 12/113 significant prostate cancers (11%), while targeted biopsies alone would have failed to diagnose 10/113 (9%). In equivocal lesions (PI-RADS 3), targeted biopsy alone would not have diagnosed 14/25 (56%) of Gleason score 7-10 cancers, whereas systematic biopsies alone would have missed 1/25 (4%). Combination with PSA density improved the area under the curve of PI-RADS from 0.822 to 0.846.

CONCLUSION

In patients with high probability mpMRI lesions, the highest detection rates of Gleason score 7-10 cancer still required combined targeted and systematic MRI/US image-fusion; however, systematic biopsy alone may be sufficient in patients with equivocal lesions. Repeated prostate biopsies may not be needed at all for patients with a low PSA density and a negative mpMRI read by experienced radiologists.

摘要

目的

在两个大型医疗中心,评估经会阴前列腺穿刺活检时,磁共振成像(MRI)和超声(US)图像融合技术下,靶向活检和系统活检对既往经直肠穿刺活检为良性的患者的检测率。

患者与方法

一项两中心前瞻性结局研究,纳入487例既往穿刺活检为良性的患者,于2012年至2015年接受经会阴MRI/US融合引导下的靶向活检和系统饱和穿刺活检。多参数MRI(mpMRI)根据前列腺影像报告和数据系统(PI-RADS)第1版进行报告。穿刺活检时检测到Gleason评分7-10分的前列腺癌为主要结局。计算阳性(PPV)和阴性(NPV)预测值及95%置信区间(95%CI)。使用McNemar检验比较靶向活检和系统活检的检测率。

结果

前列腺特异抗原(PSA)水平中位数(四分位间距)为9.0(6.7-13.4)ng/mL。343例(70%)患者报告有PI-RADS 3-5级mpMRI病变,149例(31%)检测到Gleason评分7-10分的前列腺癌。PI-RADS 3级检测Gleason评分7-10分前列腺癌的PPV(95%CI)为0.20(±0.07),PI-RADS 4级为0.32(±0.09),PI-RADS 5级为0.70(±0.08)。PI-RADS 1-2级对于Gleason评分7-10分的NPV(95%CI)为0.92(±0.04),对于Gleason评分≥4+3癌的NPV为0.99(±0.02)。仅系统活检发现125/138例(91%)Gleason评分7-10分的癌症。在mpMRI有可疑病变(PI-RADS 4-5)的患者中,仅系统活检会漏诊12/113例(11%)显著前列腺癌,而仅靶向活检会漏诊10/113例(9%)。在可疑病变(PI-RADS 3)中,仅靶向活检会漏诊14/25例(56%)Gleason评分7-10分的癌症,而仅系统活检会漏诊1/25例(4%)。联合PSA密度可使PI-RADS曲线下面积从0.822提高至0.846。

结论

对于mpMRI病变可能性高的患者,检测Gleason评分7-10分癌症的最高检测率仍需联合靶向和系统MRI/US图像融合;然而,对于可疑病变患者,仅系统活检可能就足够了。对于PSA密度低且经验丰富的放射科医生读片mpMRI为阴性的患者,可能根本无需重复前列腺穿刺活检。

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