Development and external validation of an interpretable multimodal deep learning model for 5-year mortality in high-risk stage ii colorectal cancer.

IF 2.3 3区 医学 Q2 GASTROENTEROLOGY & HEPATOLOGY
Xin Li, Lei Liang, Zhong-Hua Liu, Chun Wang, Tawfik Ali Hamood Alburiahi, Zhen-Ya Yang, Ning Xu, Jun Yang
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引用次数: 0

Abstract

Purpose: High-risk stage II colorectal cancer (CRC) shows heterogeneous outcomes despite adjuvant chemotherapy. We developed and validated an interpretable multimodal deep learning model integrating clinical data, serum biomarkers, and venous-phase CT to predict 5-year CRC-specific mortality in high-risk stage II CRC.

Methods: This retrospective, multicenter cohort included 778 high-risk stage II CRC patients from three centers, all treated with adjuvant chemotherapy and with complete preoperative clinical, biomarker, and venous-phase CT data. Patients were split into a development cohort (Centers A + B, n = 720) and an external testing cohort (Center C, n = 58). A multimodal model combining numerical (clinical + biomarker) and imaging (CT) inputs was developed and internally validated using tenfold cross-validation in the development cohort and evaluated in the external cohort. Interpretability was assessed using SHAP and Grad-CAM.

Results: In the development cohort, the multimodal model showed superior discrimination (AUC 0.89; 95% CI, 0.87-0.91) versus numerical-only (AUC 0.76) and imaging-only (AUC 0.69). In the external testing cohort (9/58 CRC-specific deaths), the multimodal model achieved an AUC of 0.88 (95% CI, 0.76-0.96). SHAP and Grad-CAM consistently highlighted age, CA125, and tumor regions on CT as key contributors.

Conclusion: This interpretable multimodal approach, using routine clinical, biomarker, and CT data, improves 5-year mortality risk stratification in high-risk stage II CRC and may inform risk-adapted surveillance and clinical decision support; prospective validation is warranted before treatment modification.

高风险ii期结直肠癌5年死亡率的可解释多模态深度学习模型的开发和外部验证
目的:高危II期结直肠癌(CRC)尽管进行了辅助化疗,但结局却不尽相同。我们开发并验证了一个可解释的多模态深度学习模型,该模型整合了临床数据、血清生物标志物和静脉期CT,以预测高风险II期CRC的5年CRC特异性死亡率。方法:该回顾性多中心队列研究包括来自三个中心的778例高危II期CRC患者,所有患者均接受了辅助化疗,并有完整的术前临床、生物标志物和静脉期CT数据。患者被分为发展队列(a + B中心,n = 720)和外部测试队列(C中心,n = 58)。开发了一个结合数值(临床+生物标志物)和成像(CT)输入的多模态模型,并在开发队列中使用十倍交叉验证进行内部验证,并在外部队列中进行评估。使用SHAP和Grad-CAM评估可解释性。结果:在发展队列中,多模态模型与仅数字模型(AUC 0.76)和仅成像模型(AUC 0.69)相比,具有更好的鉴别能力(AUC 0.89; 95% CI, 0.87-0.91)。在外部测试队列(9/58例crc特异性死亡)中,多模式模型的AUC为0.88 (95% CI, 0.76-0.96)。SHAP和Grad-CAM一致强调年龄、CA125和CT上的肿瘤区域是关键因素。结论:这种可解释的多模式方法,使用常规临床、生物标志物和CT数据,改善了高风险II期CRC的5年死亡风险分层,并可能为风险适应监测和临床决策支持提供信息;在修改治疗前需要进行前瞻性验证。
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来源期刊
CiteScore
4.90
自引率
3.60%
发文量
206
审稿时长
3-8 weeks
期刊介绍: The International Journal of Colorectal Disease, Clinical and Molecular Gastroenterology and Surgery aims to publish novel and state-of-the-art papers which deal with the physiology and pathophysiology of diseases involving the entire gastrointestinal tract. In addition to original research articles, the following categories will be included: reviews (usually commissioned but may also be submitted), case reports, letters to the editor, and protocols on clinical studies. The journal offers its readers an interdisciplinary forum for clinical science and molecular research related to gastrointestinal disease.
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