Multi-task Deep Learning Based on Longitudinal CT Images Facilitates Prediction of Lymph Node Metastasis and Survival in Chemotherapy-Treated Gastric Cancer.

IF 12.5 1区 医学 Q1 ONCOLOGY
Bingjiang Qiu,Yunlin Zheng,Shunli Liu,Ruirui Song,Lei Wu,Cheng Lu,Xianqi Yang,Wei Wang,Zaiyi Liu,Yanfen Cui
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引用次数: 0

Abstract

Accurate preoperative assessment of lymph node metastasis (LNM) and overall survival (OS) status is essential for patients with locally advanced gastric cancer (LAGC) receiving neoadjuvant chemotherapy (NAC), providing timely guidance for clinical decision-making. However, current approaches to evaluate LNM and OS have limited accuracy. In this study, we used longitudinal CT images from 1,021 LAGC patients to develop and validate a multi-task deep learning model named co-attention tri-oriented spatial Mamba (CTSMamba) to simultaneously predict LNM and OS. CTSMamba was trained and validated on 398 patients, and the performance was further validated on 623 patients at two additional centers. Notably, CTSMamba exhibited significantly more robust performance than a clinical model in predicting LNM across all of the cohorts. Additionally, integrating CTSMamba survival scores with clinical predictors further improved personalized OS prediction. These results support the potential of CTSMamba to accurately predict LNM and OS from longitudinal images, potentially providing clinicians with a tool to inform individualized treatment approaches and optimized prognostic strategies.
基于纵向CT图像的多任务深度学习有助于预测化疗后胃癌的淋巴结转移和生存。
术前准确评估局部晚期胃癌(LAGC)新辅助化疗(NAC)患者的淋巴结转移(LNM)和总生存(OS)状况,及时指导临床决策至关重要。然而,目前评估LNM和OS的方法准确度有限。在这项研究中,我们使用了1021例LAGC患者的纵向CT图像,开发并验证了一个多任务深度学习模型,称为共同注意三向空间曼巴(CTSMamba),以同时预测LNM和OS。CTSMamba在398名患者中进行了培训和验证,并在另外两个中心的623名患者中进一步验证了其性能。值得注意的是,在所有队列中,CTSMamba在预测LNM方面表现出比临床模型更为稳健的表现。此外,将CTSMamba生存评分与临床预测指标相结合,进一步改善了个性化的OS预测。这些结果支持CTSMamba从纵向图像中准确预测LNM和OS的潜力,可能为临床医生提供个性化治疗方法和优化预后策略的工具。
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来源期刊
Cancer research
Cancer research 医学-肿瘤学
CiteScore
16.10
自引率
0.90%
发文量
7677
审稿时长
2.5 months
期刊介绍: Cancer Research, published by the American Association for Cancer Research (AACR), is a journal that focuses on impactful original studies, reviews, and opinion pieces relevant to the broad cancer research community. Manuscripts that present conceptual or technological advances leading to insights into cancer biology are particularly sought after. The journal also places emphasis on convergence science, which involves bridging multiple distinct areas of cancer research. With primary subsections including Cancer Biology, Cancer Immunology, Cancer Metabolism and Molecular Mechanisms, Translational Cancer Biology, Cancer Landscapes, and Convergence Science, Cancer Research has a comprehensive scope. It is published twice a month and has one volume per year, with a print ISSN of 0008-5472 and an online ISSN of 1538-7445. Cancer Research is abstracted and/or indexed in various databases and platforms, including BIOSIS Previews (R) Database, MEDLINE, Current Contents/Life Sciences, Current Contents/Clinical Medicine, Science Citation Index, Scopus, and Web of Science.
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