基于MRI和临床特征预测前列腺癌进展风险的深度学习模型的开发和验证。

IF 5.6 Q1 ONCOLOGY
Christian Roest, Thomas C Kwee, Igle J de Jong, Ivo G Schoots, Pim van Leeuwen, Stijn W T P J Heijmink, Henk G van der Poel, Stefan J Fransen, Anindo Saha, Henkjan Huisman, Derya Yakar
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引用次数: 0

摘要

目的验证基于MRI和临床参数的深度学习(DL)预测前列腺癌(PCa)进展风险的模型,并与已建立的模型进行比较。材料与方法本回顾性研究包括1143例男性患者的1607次MRI扫描(中位年龄64岁;IQR, 59-68岁,在2012年1月至2022年5月期间因怀疑有临床意义的前列腺癌(csPCa)接受MRI检查(国际泌尿病理学学会分级bbbb1),基线MRI检查为csPCa阴性。使用基线MRI和临床参数(年龄、前列腺特异性抗原(PSA)水平、PSA密度和前列腺体积)建立DL模型来预测到PCa进展的时间(定义为随访时诊断为csPCa)。进行了内部和外部测试。通过Cox回归分析评估该模型预测csPCa进展的能力。与欧洲前列腺癌筛查随机研究(ERSPC)未来风险计算器、前列腺癌预防试验(PCPT)风险计算器和前列腺成像报告和数据系统(PI-RADS)相比,DL模型在基线MRI后5年的预测性能使用Harrell c指数进行评估。根据Kaplan-Meier曲线得出最佳随访间隔。结果DL评分预测csPCa进展(内部队列:风险比[HR], 1.97 [95% CI: 1.61, 2.41;P < .001];外部队列:HR, 1.32 [95% CI: 1.14, 1.55;P < 0.001])。该模型确定了一个亚组患者(约20%),分别在1年,2年和4年随访后,csPCa的风险为3%或更低,8%或更低,18%或更低。DL评分在内部测试中的c指数为0.68 (95% CI: 0.63, 0.74),在外部测试中为0.56 (95% CI: 0.51, 0.61),在内部测试中优于ERSPC和PCPT (P均< .001)。结论DL模型准确预测了PCa的进展,并提供了改进的风险估计,证明了其有助于低风险PCa的个性化随访的能力。关键词:MRI,前列腺癌,深度学习本文有补充材料。©RSNA, 2025年。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Development and Validation of a Deep Learning Model Based on MRI and Clinical Characteristics to Predict Risk of Prostate Cancer Progression.

Purpose To validate a deep learning (DL) model for predicting the risk of prostate cancer (PCa) progression based on MRI and clinical parameters and compare it with established models. Materials and Methods This retrospective study included 1607 MRI scans of 1143 male patients (median age, 64 years; IQR, 59-68 years) undergoing MRI for suspicion of clinically significant PCa (csPCa) (International Society of Urological Pathology grade > 1) between January 2012 and May 2022 who were negative for csPCa at baseline MRI. A DL model was developed using baseline MRI and clinical parameters (age, prostate-specific antigen [PSA] level, PSA density, and prostate volume) to predict the time to PCa progression (defined as csPCa diagnosis at follow-up). Internal and external testing was performed. The model's ability to predict progression to csPCa was assessed by Cox regression analyses. Predictive performance of the DL model up to 5 years after baseline MRI in comparison with the European Randomized Study of Screening for Prostate Cancer (ERSPC) future-risk calculator, Prostate Cancer Prevention Trial (PCPT) risk calculator, and Prostate Imaging Reporting and Data System (PI-RADS) was assessed using the Harrell C-index. Optimized follow-up intervals were derived from Kaplan-Meier curves. Results DL scores predicted csPCa progression (internal cohort: hazard ratio [HR], 1.97 [95% CI: 1.61, 2.41; P < .001]; external cohort: HR, 1.32 [95% CI: 1.14, 1.55; P < .001]). The model identified a subgroup of patients (approximately 20%) with risks for csPCa of 3% or less, 8% or less, and 18% or less after 1-, 2-, and 4-year follow-up, respectively. DL scores had a C-index of 0.68 (95% CI: 0.63, 0.74) at internal testing and 0.56 (95% CI: 0.51, 0.61) at external testing, outperforming ERSPC and PCPT (both P < .001) at internal testing. Conclusion The DL model accurately predicted PCa progression and provided improved risk estimations, demonstrating its ability to aid in personalized follow-up for low-risk PCa. Keywords: MRI, Prostate Cancer, Deep Learning Supplemental material is available for this article. ©RSNA, 2025.

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