基于统一弱监督深度学习模型的胰腺癌预后预测

IF 52.7 1区 医学 Q1 BIOCHEMISTRY & MOLECULAR BIOLOGY
Wei Yuan, Yijiang Chen, Biyue Zhu, Sen Yang, Jiayu Zhang, Ning Mao, Jinxi Xiang, Yuchen Li, Yuanfeng Ji, Xiangde Luo, Kangning Zhang, Xiaohan Xing, Shuo Kang, Dongyuan Xiao, Fang Wang, Jinkun Wu, Haiyan Zhang, Hongping Tang, Himanshu Maurya, German Corredor, Cristian Barrera, Yufei Zhou, Krunal Pandav, Junhan Zhao, Prantesh Jain, Luke Delasos, Junzhou Huang, Kailin Yang, Theodoros N. Teknos, James Lewis, Shlomo Koyfman, Nathan A. Pennell, Kun-Hsing Yu, Xiao Han, Jing Zhang, Xiyue Wang, Anant Madabhushi
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引用次数: 0

摘要

准确的预后预测对于指导癌症治疗和改善患者预后至关重要。虽然最近的研究已经证明了组织病理学图像在生存分析中的潜力,但现有的模型通常是以癌症特异性的方式开发的,缺乏广泛的外部验证,并且经常依赖于临床实践中不常用的分子数据。为了解决这些局限性,我们提出了PROGPATH,这是一个统一的模型,能够将组织病理图像特征与常规收集的临床变量相结合,以实现胰腺癌预后预测。PROGPATH采用基于图像编码基础模型的弱监督深度学习架构。形态学特征通过注意引导的多实例学习模块聚合,并通过交叉注意转换器与临床信息融合。基于路由器的分类策略进一步细化了预测性能。PROGPATH在来自15种癌症类型的6670名患者的7999张全片图像(wsi)上进行了训练,并在17个外部队列中进行了广泛验证,其中包括来自三大洲8个财团和机构的4441名患者的7374张全片图像,涵盖了12种癌症类型。与最先进的多模态预后预测模型相比,PROGPATH始终取得了卓越的性能。它在不同癌症类型和分层亚组(包括早期和晚期患者、治疗队列(放疗和药物治疗)和生物标志物定义的亚组)中显示出很强的普遍性和稳健性。我们进一步通过确定对PROGPATH风险预测至关重要的病理模式(如细胞分化程度和坏死程度)来提供模型的可解释性。总之,这些结果突出了PROGPATH在支持胰腺癌预后预测和个性化癌症管理策略方面的潜力。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Pancancer outcome prediction via a unified weakly supervised deep learning model

Pancancer outcome prediction via a unified weakly supervised deep learning model

Accurate prognosis prediction is essential for guiding cancer treatment and improving patient outcomes. While recent studies have demonstrated the potential of histopathological images in survival analysis, existing models are typically developed in a cancer-specific manner, lack extensive external validation, and often rely on molecular data that are not routinely available in clinical practice. To address these limitations, we present PROGPATH, a unified model capable of integrating histopathological image features with routinely collected clinical variables to achieve pancancer prognosis prediction. PROGPATH employs a weakly supervised deep learning architecture built upon the foundation model for image encoding. Morphological features are aggregated through an attention-guided multiple instance learning module and fused with clinical information via a cross-attention transformer. A router-based classification strategy further refines the prediction performance. PROGPATH was trained on 7999 whole-slide images (WSIs) from 6,670 patients across 15 cancer types, and extensively validated on 17 external cohorts with a total of 7374 WSIs from 4441 patients, covering 12 cancer types from 8 consortia and institutions across three continents. PROGPATH achieved consistently superior performance compared with state-of-the-art multimodal prognosis prediction models. It demonstrated strong generalizability across cancer types and robustness in stratified subgroups, including early- and advanced-stage patients, treatment cohorts (radiotherapy and pharmaceutical therapy), and biomarker-defined subsets. We further provide model interpretability by identifying pathological patterns critical to PROGPATH’s risk predictions, such as the degree of cell differentiation and extent of necrosis. Together, these results highlight the potential of PROGPATH to support pancancer outcome prediction and inform personalized cancer management strategies.

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来源期刊
Signal Transduction and Targeted Therapy
Signal Transduction and Targeted Therapy Biochemistry, Genetics and Molecular Biology-Genetics
CiteScore
44.50
自引率
1.50%
发文量
384
审稿时长
5 weeks
期刊介绍: Signal Transduction and Targeted Therapy is an open access journal that focuses on timely publication of cutting-edge discoveries and advancements in basic science and clinical research related to signal transduction and targeted therapy. Scope: The journal covers research on major human diseases, including, but not limited to: Cancer,Cardiovascular diseases,Autoimmune diseases,Nervous system diseases.
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