Li Eric V, Kumar Sai K, Aguiar Jonathan A, Siddiqui Mohammad R, Neill Clayton, Sun Zequn, Schaeffer Edward M, Jawahar Anugayathri, Ross Ashley E, Patel Hiten D
Department of Urology, Feinberg School of Medicine Northwestern University Chicago Illinois USA.
Department of Preventive Medicine-Division of Biostatistics Northwestern University Feinberg School of Medicine Chicago Illinois USA.
BJUI Compass. 2024 Aug 4;5(9):865-873. doi: 10.1002/bco2.415. eCollection 2024 Sep.
This study aimed to evaluate the association of dynamic contrast enhancement (DCE) with clinically significant prostate cancer (csPCa, Gleason Grade Group ≥2) and compare biparametric magnetic resonance imaging (bpMRI) and multiparametric MRI (mpMRI) nomograms.
SUBJECTS/PATIENTS AND METHODS: We identified a retrospective cohort of biopsy naïve patients who underwent pre-biopsy MRI separated by individual MRI series from 2018 to 2022. csPCa detection rates were calculated for patients with peripheral zone (PZ) lesions scored 3-5 on diffusion weighted imaging (DWI) with available DCE (annotated as - or +). bpMRI Prostate Imaging Reporting and Data System (PIRADS) (3 = 3-, 3+; 4 = 4-, 4+; 5 = 5-, 5+) and mpMRI PIRADS (3 = 3-; 4 = 3+, 4-, 4+; 5 = 5-, 5+) approaches were compared in multivariable logistic regression models. Nomograms for detection of csPCa and ≥GG3 PCa incorporating all biopsy naïve patients who underwent prostate MRI were generated based on available serum biomarkers [PHI, % free prostate-specific antigen (PSA), or total PSA] and validated with an independent cohort.
Patients ( = 1010) with highest PIRADS lesion in PZ were included in initial analysis with 127 (12.6%) classified as PIRADS 3+ (PIRADS 3 on bpMRI but PIRADS 4 on mpMRI). On multivariable analysis, PIRADS 3+ lesions were associated with higher csPCa rates compared to PIRADS 3- (3+ vs. 3-: OR 1.86, = 0.024), but lower csPCa rates compared to PIRADS DWI 4 lesions (4 vs. 3+: OR 2.39, < 0.001). csPCa rates were 19% (3-), 31% (3+), 41.5% (4-), 65.9% (4+), 62.5% (5-), and 92.3% (5+). bpMRI nomograms were non-inferior to mpMRI nomograms in the development ( = 1410) and independent validation ( = 353) cohorts. Risk calculators available at: https://rossnm1.shinyapps.io/MynMRIskCalculator/.
While DCE positivity by itself was associated with csPCa among patients with highest PIRADS lesions in the PZ, nomogram comparisons suggest that there is no significant difference in performance of bpMRI and mpMRI. bpMRI may be considered as an alternative to mpMRI for prostate cancer evaluation in many situations.
本研究旨在评估动态对比增强(DCE)与临床显著性前列腺癌(csPCa, Gleason分级组≥2)之间的关联,并比较双参数磁共振成像(bpMRI)和多参数磁共振成像(mpMRI)列线图。
受试者/患者与方法:我们确定了一组2018年至2022年期间未接受过活检且在活检前接受过MRI检查的患者的回顾性队列,这些患者的MRI检查按个体MRI序列分类。计算了外周带(PZ)病变在扩散加权成像(DWI)上评分为3-5且有可用DCE(标注为-或+)的患者的csPCa检出率。在多变量逻辑回归模型中比较了bpMRI前列腺影像报告和数据系统(PIRADS)(3 = 3-,3+;4 = 4-,4+;5 = 5-,5+)和mpMRI PIRADS(3 = 3-;4 = 3+,4-,4+;5 = 5-,5+)方法。基于可用的血清生物标志物[前列腺健康指数(PHI)、游离前列腺特异性抗原(PSA)百分比或总PSA]生成了纳入所有接受过前列腺MRI检查的未接受过活检患者的csPCa和≥GG3 PCa检测列线图,并在一个独立队列中进行了验证。
最初分析纳入了PZ中PIRADS病变最高的患者(n = 1010),其中127例(12.6%)被分类为PIRADS 3+(bpMRI上为PIRADS 3,但mpMRI上为PIRADS 4)。在多变量分析中,与PIRADS 3-相比,PIRADS 3+病变与更高的csPCa发生率相关(3+ vs. 3-:比值比[OR] 1.86,P = 0.024),但与PIRADS DWI 4病变相比,csPCa发生率较低(4 vs. 3+:OR 2.39,P < 0.001)。csPCa发生率分别为19%(3-)、31%(3+)、41.5%(4-)、65.9%(4+)、62.5%(5-)和92.3%(5+)。在开发队列(n = 1410)和独立验证队列(n = 353)中,bpMRI列线图不劣于mpMRI列线图。风险计算器可在以下网址获取:https://rossnm1.shinyapps.io/MynMRIskCalculator/。
虽然在PZ中PIRADS病变最高的患者中,DCE阳性本身与csPCa相关,但列线图比较表明,bpMRI和mpMRI的性能没有显著差异。在许多情况下,bpMRI可被视为mpMRI用于前列腺癌评估的替代方法。