Department of Urology and Kidney Transplantation, Conception Academic Hospital, Aix-Marseille University, APHM, Marseille, France.
Department of Radiology and Medical Imaging, Conception Academic Hospital, Aix-Marseille University, APHM, Marseille, France.
Abdom Radiol (NY). 2020 Dec;45(12):4160-4165. doi: 10.1007/s00261-020-02728-8. Epub 2020 Sep 9.
To evaluate the negative predictive value (NPV) of multiparametric magnetic resonance imaging (mpMRI), alone or combined with Prostate-Specific Antigen density (PSAd) to exclude clinically significant prostate cancer (csPCa).
We performed a retrospective chart review of all the patients who had transrectal ultrasound-guided biopsy (TRUSGB) in our center between January 2014 and March 2019. We included patients who had nonsuspicious prebiopsy mpMRI defined as Prostate Imaging-Reporting and Data System (PI-RADS) ≤ 2. MRI was performed using a 1.5 or 3-Tesla Magnetic Resonance scanners with external phased-array coil. The primary outcome was the detection of csPCa, defined as a Gleason score 3 + 4 (ISUP 2) or higher on at least one biopsy core.
One hundred and ninety-one consecutive men (median age: 65 years, median PSA level: 9.3 ng/mL) underwent TRUSGB following negative prebiopsy mpMRI corresponding to 126 (66%) biopsy-naïve patients, 36 (18.8%) patients with prior negative biopsy, and 29 (15.2%) patients under active surveillance with confirmatory biopsies. The overall PCa and csPCA detection rates were 26.7% and 5.2%, conferring a NPV of 73.3% and 94.8%, respectively. The NPV of negative mpMRI improved to 95.8% in patients with PSAd < 0.15 ng/mL/cm and to 100% in patients with PSAd < 0.10 ng/mL/cm.
A negative prebiopsy mpMRI had an overall NPV of 94.8% for csPCa when mpMRI was used alone to 95.8% when combined with PSAd < 0.15 ng/mL/cm. Future studies are needed to balance the low benefit of a biopsy in this indication with the morbidity of the procedure.
评估多参数磁共振成像(mpMRI)单独或联合前列腺特异性抗原密度(PSAd)用于排除临床显著前列腺癌(csPCa)的阴性预测值(NPV)。
我们对 2014 年 1 月至 2019 年 3 月在我们中心接受经直肠超声引导活检(TRUSGB)的所有患者进行了回顾性图表审查。我们纳入了经活检前 MRI 检查未见可疑表现的患者,定义为前列腺影像报告和数据系统(PI-RADS)≤2 分。MRI 检查采用 1.5 或 3T 磁共振扫描仪和外部相控阵线圈进行。主要结局是检测 csPCa,定义为至少一个活检核心的 Gleason 评分 3+4(ISUP 2)或更高。
191 例连续男性(中位年龄:65 岁,中位 PSA 水平:9.3ng/mL)在经活检前阴性 mpMRI 后接受了 TRUSGB,其中 126 例(66%)为活检初治患者,36 例(18.8%)为先前阴性活检患者,29 例(15.2%)为接受确认性活检的主动监测患者。总的前列腺癌和 csPCA 检出率分别为 26.7%和 5.2%,NPV 分别为 73.3%和 94.8%。当单独使用 mpMRI 时,PSAd<0.15ng/mL/cm 的患者阴性 mpMRI 的 NPV 提高至 95.8%,PSAd<0.10ng/mL/cm 的患者 NPV 提高至 100%。
单独使用 mpMRI 时,活检前阴性 mpMRI 对 csPCa 的总体 NPV 为 94.8%,当与 PSAd<0.15ng/mL/cm 联合使用时 NPV 为 95.8%。需要进一步研究来平衡在该适应证中进行活检的低获益与操作的发病率。