Utility of dynamic contrast enhancement for clinically significant prostate cancer detection

IF 1.6 Q3 UROLOGY & NEPHROLOGY
BJUI compass Pub Date : 2024-08-04 DOI:10.1002/bco2.415
Eric V. Li, Sai K. Kumar, Jonathan A. Aguiar, Mohammad R. Siddiqui, Clayton Neill, Zequn Sun, Edward M. Schaeffer, Anugayathri Jawahar, Ashley E. Ross, Hiten D. Patel
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引用次数: 0

Abstract

Objective

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.

Results

Patients (n = 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, p = 0.024), but lower csPCa rates compared to PIRADS DWI 4 lesions (4 vs. 3+: OR 2.39, p < 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 (n = 1410) and independent validation (n = 353) cohorts. Risk calculators available at: https://rossnm1.shinyapps.io/MynMRIskCalculator/.

Conclusion

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.

Abstract Image

动态对比度增强技术在临床重大前列腺癌检测中的应用
目的 本研究旨在评估动态对比增强(DCE)与有临床意义的前列腺癌(csPCa,格里森分级组≥2)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)提名图。 受试者/患者和方法 我们确定了一个回顾性队列,其中包括 2018 年至 2022 年期间接受活检前 MRI 检查的未接受活检的患者,这些患者按单个 MRI 系列分开。我们计算了在弥散加权成像(DWI)上评分为 3-5 的外周区(PZ)病变患者的 csPCa 检出率,并提供了 DCE(注释为 - 或 +)。在多变量逻辑回归模型中比较了 bpMRI Prostate Imaging Reporting and Data System (PIRADS) (3 = 3-, 3+; 4 = 4-, 4+; 5 = 5-, 5+) 和 mpMRI PIRADS (3 = 3-; 4 = 3+, 4-, 4+; 5 = 5-, 5+) 方法。根据现有的血清生物标记物[PHI、游离前列腺特异性抗原 (PSA) % 或总 PSA]生成了用于检测 csPCa 和 ≥GG3 PCa 的提名图,并通过独立队列进行了验证。 结果 PZ 中 PIRADS 病变最高的患者(n = 1010)被纳入初步分析,其中 127 例(12.6%)被归类为 PIRADS 3+(bpMRI 上 PIRADS 3,但 mpMRI 上 PIRADS 4)。在多变量分析中,与 PIRADS 3- 相比,PIRADS 3+ 病变与较高的 csPCa 发生率相关(3+ vs. 3-: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.csPCa 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 推测图不劣于 mpMRI 推测图。风险计算器见:https://rossnm1.shinyapps.io/MynMRIskCalculator/。 结论 虽然在 PZ 中 PIRADS 病变最高的患者中,DCE 阳性本身与 csPCa 有关,但提名图比较表明 bpMRI 和 mpMRI 的性能没有显著差异。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
CiteScore
2.30
自引率
0.00%
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0
审稿时长
12 weeks
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