金丝雀前列腺主动监测研究中1级前列腺癌患者诊断后第二次监测活检的磁共振成像。

Meera R Chappidi,Lisa F Newcomb,Yingye Zheng,Menghan Liu,Jeannette M Schenk,Kehao Zhu,Claire M de la Calle,James D Brooks,Peter R Carroll,Atreya Dash,Christopher P Filson,Martin E Gleave,Michael A Liss,Frances Martin,Jesse K McKenney,Todd M Morgan,Andrew A Wagner,Peter S Nelson,Daniel W Lin
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摘要

目的:在主动监测(AS)期间,尚无明确的MRI使用指南。我们的目的是评估确诊活检患者与未确诊活检患者的MRI表现。方法Canary PASS的Gleason分级组(GG) 1患者接受mri知情活检2(定义为诊断后的第二次监测活检),分为有mri知情活检组和无mri知情活检组。主要结局是在mri通知的活检2中重新分类(≥GG2)。比较两组间重分类率和位置(系统核、靶核、两者)。单变量和多变量逻辑回归确定了重分类的预测因子。结果(n=101)与(n=103)未进行mri活检的患者在第2次活检时的重分类率较低(21%对36%,p=0.017),重分类时的GG较低(95%对73%的重分类为GG2, p=0.039)。在多变量模型中,mri通知活检2时PI-RADS 4-5与重新分类的几率增加相关(OR=2.04 95%CI[1.04-4.05])。活检2期MRI阴性预测值分别为87% (95%CI[78-96])和73% (95%CI[61-85])。在有和没有做过MRI的患者中,只有36%和19%的患者通过靶核识别出了重分类位置(p=0.4)。通过系统核识别重分类位置的患者分别为36%和58% (p=0.4)。结论这些结果支持MRI在第2次活检中使用,并提示阴性监测MRI不应取代第2次活检。在有或没有既往AS MRI的患者中,应在活检2时进行靶向和系统核心检查。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Magnetic Resonance Imaging at second surveillance biopsy after diagnosis in patients with Grade Group 1 prostate cancer in the Canary Prostate Active Surveillance Study.
PURPOSE No clear guidelines exist regarding MRI use after confirmatory biopsy during active surveillance (AS). Our objective was to evaluate MRI performance after confirmatory biopsy in patients with vs. without prior MRI-informed biopsy. METHODS Patients in Canary PASS with Gleason grade group (GG) 1 disease undergoing MRI-informed Biopsy 2, defined as second surveillance biopsy after diagnosis, were separated into prior vs. no prior MRI-informed biopsy groups. Primary outcome was reclassification (≥GG2) at MRI-informed Biopsy 2. Reclassification rates and location (systematic cores, targeted cores, both) were compared between groups. Univariable and multivariable logistic regression identified predictors of reclassification. RESULTS Patients with (n=101) vs. without (n=103) prior MRI-informed biopsy had lower reclassification rates at Biopsy 2 (21% vs. 36%, p=0.017) and lower GG at reclassification (95% vs. 73% of reclassifications to GG2, p=0.039). In multivariable modeling, PI-RADS 4-5 at MRI-informed Biopsy 2 was associated with increased odds of reclassification (OR=2.04 95%CI [1.04-4.05]). The negative predictive value of MRI at Biopsy 2 was 87% (95%CI[78-96]) and 73% (95%CI[61-85]) in with vs. without prior MRI groups, respectively. Reclassification location was identified by targeted cores only in 36% vs. 19% of patients with vs. without prior MRI, respectively (p=0.4). Reclassification location was identified by systematic cores only in 36% vs. 58% of patients with vs. without prior MRI, respectively (p=0.4). CONCLUSIONS These results support MRI use at Biopsy 2 and suggest negative surveillance MRI should not replace Biopsy 2. Both targeted and systematic cores should be taken at Biopsy 2 in patients with and without prior MRI on AS.
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