Yueyue Li, Ximiao Wang, Qiuying Chen, Hua Xiao, Yilong Huang, Liebin Huang, Lian Jian, Wansheng Long, Bao Feng, Shuixing Zhang
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{"title":"基于肿瘤和内脏脂肪组织CT特征的深度学习模型预测浆膜浸润性胃癌根治性胃切除术后腹膜转移风险","authors":"Yueyue Li, Ximiao Wang, Qiuying Chen, Hua Xiao, Yilong Huang, Liebin Huang, Lian Jian, Wansheng Long, Bao Feng, Shuixing Zhang","doi":"10.1148/rycan.250353","DOIUrl":null,"url":null,"abstract":"<p><p>Purpose To develop and validate a deep learning model integrating tumor and visceral adipose tissue (VAT) CT scan features with clinical indicators to predict postoperative peritoneal metastasis in serosa-invasive gastric cancer. Materials and Methods This multicenter, retrospective study between April 2008 and January 2018 included patients with pathologically confirmed serosa-invasive gastric cancer. Patients were divided into training, internal test, and independent external test sets. Tumor and VAT regions were segmented at preoperative CT. Deep features were extracted using a ResNet18 network. A fused tumor-VAT deep learning signature (F-DLS) was generated, incorporating clinical variables into a multimodal deep learning radiomics model (MDLR) using a sparse Bayesian extreme learning machine. Model performance was assessed using receiver operating characteristic curve, integrated discrimination improvement, calibration, decision curve analysis, and recurrence-free survival. Results Among 416 patients (mean age, 56.6 years ± 11.6; 66.1% male patients), the F-DLS achieved area under the receiver operating characteristic curve (AUC) values of 0.81 (95% CI: 0.73, 0.88) in the internal test set and 0.79 (95% CI: 0.71, 0.86) in the external test set. Compared with the tumor tissue DLS and VAT-DLS, the F-DLS showed numerically higher AUCs without statistical significance. The MDLR achieved the strongest predictive performance, with AUCs of 0.86 (95% CI: 0.79, 0.92) in the internal test set and 0.86 (95% CI: 0.78, 0.92) in the external test set. The MDLR statistically significantly outperformed clinical and deep learning-only models (integrated discrimination improvement, <i>P</i> < .001), showed good calibration, and provided favorable net benefit on decision curve analysis. High-risk patients identified by the MDLR had significantly shorter recurrence-free survival (log-rank <i>P</i> < .001). Conclusion The MDLR integrating CT scan features and clinical indicators enabled noninvasive prediction of peritoneal metastasis risk in serosa-invasive gastric cancer and may facilitate postoperative risk stratification. <b>Keywords:</b> Gastric Cancer, Peritoneal Metastasis, CT, Visceral Adipose Tissue, Deep Learning <i>Supplemental material is available for this article.</i> © RSNA, 2026.</p>","PeriodicalId":20786,"journal":{"name":"Radiology. Imaging cancer","volume":"8 3","pages":"e250353"},"PeriodicalIF":5.6000,"publicationDate":"2026-05-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Deep Learning Model Based on Tumor and Visceral Adipose Tissue CT Features for Predicting Peritoneal Metastasis Risk after Radical Gastrectomy in Serosa-Invasive Gastric Cancer.\",\"authors\":\"Yueyue Li, Ximiao Wang, Qiuying Chen, Hua Xiao, Yilong Huang, Liebin Huang, Lian Jian, Wansheng Long, Bao Feng, Shuixing Zhang\",\"doi\":\"10.1148/rycan.250353\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><p>Purpose To develop and validate a deep learning model integrating tumor and visceral adipose tissue (VAT) CT scan features with clinical indicators to predict postoperative peritoneal metastasis in serosa-invasive gastric cancer. Materials and Methods This multicenter, retrospective study between April 2008 and January 2018 included patients with pathologically confirmed serosa-invasive gastric cancer. Patients were divided into training, internal test, and independent external test sets. Tumor and VAT regions were segmented at preoperative CT. Deep features were extracted using a ResNet18 network. A fused tumor-VAT deep learning signature (F-DLS) was generated, incorporating clinical variables into a multimodal deep learning radiomics model (MDLR) using a sparse Bayesian extreme learning machine. Model performance was assessed using receiver operating characteristic curve, integrated discrimination improvement, calibration, decision curve analysis, and recurrence-free survival. Results Among 416 patients (mean age, 56.6 years ± 11.6; 66.1% male patients), the F-DLS achieved area under the receiver operating characteristic curve (AUC) values of 0.81 (95% CI: 0.73, 0.88) in the internal test set and 0.79 (95% CI: 0.71, 0.86) in the external test set. Compared with the tumor tissue DLS and VAT-DLS, the F-DLS showed numerically higher AUCs without statistical significance. The MDLR achieved the strongest predictive performance, with AUCs of 0.86 (95% CI: 0.79, 0.92) in the internal test set and 0.86 (95% CI: 0.78, 0.92) in the external test set. The MDLR statistically significantly outperformed clinical and deep learning-only models (integrated discrimination improvement, <i>P</i> < .001), showed good calibration, and provided favorable net benefit on decision curve analysis. High-risk patients identified by the MDLR had significantly shorter recurrence-free survival (log-rank <i>P</i> < .001). Conclusion The MDLR integrating CT scan features and clinical indicators enabled noninvasive prediction of peritoneal metastasis risk in serosa-invasive gastric cancer and may facilitate postoperative risk stratification. <b>Keywords:</b> Gastric Cancer, Peritoneal Metastasis, CT, Visceral Adipose Tissue, Deep Learning <i>Supplemental material is available for this article.</i> © RSNA, 2026.</p>\",\"PeriodicalId\":20786,\"journal\":{\"name\":\"Radiology. Imaging cancer\",\"volume\":\"8 3\",\"pages\":\"e250353\"},\"PeriodicalIF\":5.6000,\"publicationDate\":\"2026-05-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Radiology. Imaging cancer\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.1148/rycan.250353\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q1\",\"JCRName\":\"ONCOLOGY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Radiology. Imaging cancer","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1148/rycan.250353","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"ONCOLOGY","Score":null,"Total":0}
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