Next-generation AI for visually occult pancreatic cancer detection in a low-prevalence setting with longitudinal stability and multi-institutional generalisability.

IF 25.8 1区 医学 Q1 GASTROENTEROLOGY & HEPATOLOGY
Gut Pub Date : 2026-04-28 DOI:10.1136/gutjnl-2025-337266
Sovanlal Mukherjee,Ajith Antony,Nandakumar G Patnam,Kamaxi H Trivedi,Aashna Karbhari,Khurram Khaliq Bhinder,Armin Zarrintan,Joel G Fletcher,Mark Truty,Matthew P Johnson,Suresh T Chari,Ajit Harishkumar Goenka
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引用次数: 0

Abstract

BACKGROUND Failure of conventional imaging to detect pancreatic ductal adenocarcinoma (PDA) at its visually occult pre-diagnostic stage is a primary barrier to improving its otherwise poor rate of survival. OBJECTIVE To develop and validate the Radiomics-based Early Detection MODel (REDMOD), an AI framework to identify subvisual radiomic signatures of pre-diagnostic PDA on standard-of-care CT. DESIGNS REDMOD was trained on a multi-institutional cohort (n=969; 156 pre-diagnostic, 813 control) and tested on an independent set (n=493; 63 pre-diagnostic, 430 control), simulating a low prevalence (~1:6) early detection paradigm. The fully automated framework couples AI-driven segmentation with a heterogeneous ensemble architecture trained on a 40-feature radiomic signature derived from Synthetic Minority Over-sampling Technique (SMOTE)-balanced data. A tunable Youden Index-optimised classification threshold enables performance calibration without retraining. Validation included direct comparison with radiologists, longitudinal test-retest analysis and external specificity validation across two independent cohorts (n=539 and n=80). RESULTS On an independent test set (n=493), REDMOD identified occult PDA (AUC 0.82; 73.0% sensitivity) at a median 475-day lead time. This represented nearly twofold higher sensitivity than radiologists (38.9%; p<0.001), which grew to nearly threefold (68.0% vs 23.0%) at >24 months lead time. REDMOD showed strong longitudinal stability (90-92% concordance) and generalisable specificity across multi-institutional (81.3%; n=539) and public (87.5%; n=80) datasets. Mechanistic analyses confirmed predictive power derived principally from multi-scale wavelet-filtered textural features (90% of selected signature), which outperformed unfiltered features (AUC 0.82 vs 0.74; p=0.007) in capturing subvisual architectural disruptions. CONCLUSIONS REDMOD is an automated, mechanistically grounded, longitudinally stable, externally validated AI that surpasses radiologists for PDA detection at its visually occult pre-diagnostic stage. These attributes position it for prospective validation in high-risk cohorts, a necessary step towards shifting the paradigm from late-stage symptomatic diagnosis to proactive pre-clinical interception.
下一代人工智能在低患病率环境下用于视觉隐匿性胰腺癌检测,具有纵向稳定性和多机构通用性。
背景:在视觉上隐匿的胰腺导管腺癌(PDA)的诊断前阶段,常规影像学检查的失败是提高其低生存率的主要障碍。目的开发并验证基于放射组学的早期检测模型(REDMOD),这是一个人工智能框架,用于识别标准护理CT上PDA诊断前的亚视觉放射学特征。DESIGNSREDMOD在多机构队列(n=969; 156个预诊断,813个对照)中进行训练,并在独立组(n=493; 63个预诊断,430个对照)中进行测试,模拟低患病率(~1:6)早期检测范式。完全自动化的框架将人工智能驱动的分割与异构集成架构结合在一起,该架构训练了来自合成少数过采样技术(SMOTE)平衡数据的40个特征放射性特征。可调的优登指数优化分类阈值使性能校准无需再培训。验证包括与放射科医生的直接比较,纵向测试-再测试分析和两个独立队列(n=539和n=80)的外部特异性验证。结果在一个独立的测试集(n=493)中,REDMOD在中位475天的提前期识别出隐匿性PDA (AUC 0.82,灵敏度73.0%)。这比放射科医生(38.9%,提前24个月)的敏感度高出近两倍。REDMOD在多机构(81.3%,n=539)和公共(87.5%,n=80)数据集中显示出很强的纵向稳定性(90-92%一致性)和普遍特异性。机制分析证实,预测能力主要来自多尺度小波滤波的纹理特征(90%的选定特征),在捕捉亚视觉建筑破坏方面优于未滤波的特征(AUC 0.82 vs 0.74; p=0.007)。结论:sredmod是一种自动化的、机械基础的、纵向稳定的、外部验证的人工智能,在视觉上隐蔽的PDA预诊断阶段,它超过了放射科医生。这些特性使其能够在高风险人群中进行前瞻性验证,这是将范式从晚期症状诊断转变为前瞻性临床前拦截的必要步骤。
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
Gut
Gut 医学-胃肠肝病学
CiteScore
45.70
自引率
2.40%
发文量
284
审稿时长
1.5 months
期刊介绍: Gut is a renowned international journal specializing in gastroenterology and hepatology, known for its high-quality clinical research covering the alimentary tract, liver, biliary tree, and pancreas. It offers authoritative and current coverage across all aspects of gastroenterology and hepatology, featuring articles on emerging disease mechanisms and innovative diagnostic and therapeutic approaches authored by leading experts. As the flagship journal of BMJ's gastroenterology portfolio, Gut is accompanied by two companion journals: Frontline Gastroenterology, focusing on education and practice-oriented papers, and BMJ Open Gastroenterology for open access original research.
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