Department of Radiology and Biomedical Imaging, University of California-San Francisco, San Francisco, California.
Department of Urology, University of California-San Francisco, San Francisco, California.
J Urol. 2018 Mar;199(3):699-705. doi: 10.1016/j.juro.2017.09.075. Epub 2017 Sep 20.
The purpose of this study was to estimate the impact of lesion visibility with transrectal ultrasound on the prediction of clinically significant prostate cancer with transrectal ultrasound-magnetic resonance imaging fusion biopsy.
This HIPAA (Health Insurance Portability and Accountability Act) compliant, institutional review board approved, retrospective study was performed in 178 men who were 64.7 years old with prostate specific antigen 8.9 ng/ml. They underwent transrectal ultrasound-magnetic resonance imaging fusion biopsy from January 2013 to September 2016. Visible lesions on magnetic resonance imaging were assigned a PI-RADS™ (Prostate Imaging Reporting and Data System), version 2 score of 3 or greater. Transrectal ultrasound was positive when a hypoechoic lesion was identified. We used a 3-level, mixed effects logistic regression model to determine how transrectal ultrasound-magnetic resonance imaging concordance predicted the presence of clinically significant prostate cancer. The diagnostic performance of the 2 methods was estimated using ROC curves.
A total of 1,331 sextants were targeted by transrectal ultrasound-magnetic resonance imaging fusion or systematic biopsies, of which 1,037 were negative, 183 were Gleason score 3 + 3 and 111 were Gleason score 3 + 4 or greater. Clinically significant prostate cancer was diagnosed by transrectal ultrasound and magnetic resonance imaging alone at 20.5% and 19.7% of these locations, respectively. Men with positive imaging had higher odds of clinically significant prostate cancer than men without visible lesions regardless of modality (transrectal ultrasound OR 14.75, 95% CI 5.22-41.69, magnetic resonance imaging OR 12.27, 95% CI 6.39-23.58 and the 2 modalities OR 28.68, 95% CI 14.45-56.89, all p <0.001). The ROC AUC to detect clinically significant prostate cancer using the 2 methods (0.85, 95% CI 0.81-0.89) was statistically greater than that of transrectal ultrasound alone (0.80, 95% CI 0.76-0.85, p = 0.001) and magnetic resonance imaging alone (0.83, 95% CI 0.79-0.87, p = 0.04). The sensitivity and specificity of transrectal ultrasound were 42.3% and 91.6%, and the sensitivity and specificity of magnetic resonance imaging were 62.2% and 84.1%, respectively.
Lesion visibility on magnetic resonance imaging or transrectal ultrasound denotes a similar probability of clinically significant prostate cancer. This probability is greater when each examination is positive.
本研究旨在评估经直肠超声(TRUS)下病灶可视性对经直肠超声-磁共振成像(TRUS-MRI)融合活检预测临床显著前列腺癌的影响。
本 HIPAA(健康保险便携性和责任法案)合规、机构审查委员会批准的回顾性研究纳入了 178 名年龄为 64.7 岁、前列腺特异抗原为 8.9ng/ml 的男性。他们于 2013 年 1 月至 2016 年 9 月接受了经直肠超声-MRI 融合活检。MRI 上可见病灶被分配 PI-RADS™(前列腺成像报告和数据系统)评分 3 或更高。当发现低回声病灶时,TRUS 呈阳性。我们使用 3 级混合效应逻辑回归模型来确定 TRUS-MRI 一致性如何预测临床显著前列腺癌的存在。使用 ROC 曲线估计两种方法的诊断性能。
共有 1331 个六区被 TRUS-MRI 融合或系统活检靶向,其中 1037 个为阴性,183 个为 Gleason 评分 3+3,111 个为 Gleason 评分 3+4 或更高。单独通过 TRUS 和 MRI 诊断的临床显著前列腺癌分别为 20.5%和 19.7%。无论采用何种方式(TRUS OR 14.75,95%CI 5.22-41.69,MRI OR 12.27,95%CI 6.39-23.58,两种方式联合 OR 28.68,95%CI 14.45-56.89,均 p<0.001),影像学阳性的患者比无可见病灶的患者具有更高的临床显著前列腺癌的几率。使用两种方法(0.85,95%CI 0.81-0.89)检测临床显著前列腺癌的 ROC AUC 大于单独使用 TRUS(0.80,95%CI 0.76-0.85,p=0.001)和 MRI(0.83,95%CI 0.79-0.87,p=0.04)。TRUS 的敏感性和特异性分别为 42.3%和 91.6%,MRI 的敏感性和特异性分别为 62.2%和 84.1%。
MRI 或 TRUS 下病灶可视性表示具有相似的临床显著前列腺癌发生概率。当两种检查均为阳性时,这种概率更高。