Ang Li , Junqing Lin , Lili Lin , Jianqiang Ye , Zhongyou Ji , Han Jiang
{"title":"基于PET/CT放射组学预测体积等效食管鳞状细胞癌患者T2/T3分期","authors":"Ang Li , Junqing Lin , Lili Lin , Jianqiang Ye , Zhongyou Ji , Han Jiang","doi":"10.1016/j.cmpb.2025.108988","DOIUrl":null,"url":null,"abstract":"<div><h3>Objectives</h3><div>To develop and externally validate PET/CT-based radiomic models for predicting tumor invasion depth (≤T2 vs. ≥T3) in patients with esophageal squamous cell carcinoma (ESCC) with volume-matched tumors.</div></div><div><h3>Methods</h3><div>Semiautomatic segmentation was performed on <sup>18</sup>F-FDG PET images, and radiomic features were extracted from PET and coregistered CT scans. Feature reproducibility was evaluated with the intraclass correlation coefficient (ICC), which showed excellent agreement (ICC > 0.95). Propensity score matching (PSM) was applied to control for tumor volume and patient demographics. Dimensionality reduction was conducted using principal component analysis (PCA), followed by feature selection via LASSO and MRMR. Logistic regression (LR), linear discriminant analysis (LDA), support vector machine (SVM), and random forest (RF) models were constructed. Model performance was assessed on internal and independent external cohorts.</div></div><div><h3>Results</h3><div>In the internal validation, the PET and combined PET/CT radiomic models outperformed the CT-alone models, with the LDA and LR classifiers achieving area under the ROC curve (AUC) greater than 0.97. In the external validation, only the models based on PET features maintained good predictive performance (LR AUC 0.8438, accuracy 81.25 %; LDA AUC 0.8281, accuracy 87.5 %). Models built on CT or combined PET/CT features failed to produce valid results, defaulting to single-class predictions. PET feature-based models demonstrated stable generalizability across datasets.</div></div><div><h3>Conclusions</h3><div>Radiomic models based on PET features and LDA or LR classifiers can accurately predict tumor invasion depth in patients with volume-equivalent ESCC and show strong external generalizability. CT or combined feature models may not be reliable under stringent tumor volume constraints.</div></div>","PeriodicalId":10624,"journal":{"name":"Computer methods and programs in biomedicine","volume":"271 ","pages":"Article 108988"},"PeriodicalIF":4.8000,"publicationDate":"2025-07-24","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Prediction of T2/T3 Staging in Patients with Volume-Equivalent Esophageal Squamous Cell Carcinoma on the Basis of PET/CT Radiomics\",\"authors\":\"Ang Li , Junqing Lin , Lili Lin , Jianqiang Ye , Zhongyou Ji , Han Jiang\",\"doi\":\"10.1016/j.cmpb.2025.108988\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><h3>Objectives</h3><div>To develop and externally validate PET/CT-based radiomic models for predicting tumor invasion depth (≤T2 vs. ≥T3) in patients with esophageal squamous cell carcinoma (ESCC) with volume-matched tumors.</div></div><div><h3>Methods</h3><div>Semiautomatic segmentation was performed on <sup>18</sup>F-FDG PET images, and radiomic features were extracted from PET and coregistered CT scans. Feature reproducibility was evaluated with the intraclass correlation coefficient (ICC), which showed excellent agreement (ICC > 0.95). Propensity score matching (PSM) was applied to control for tumor volume and patient demographics. Dimensionality reduction was conducted using principal component analysis (PCA), followed by feature selection via LASSO and MRMR. Logistic regression (LR), linear discriminant analysis (LDA), support vector machine (SVM), and random forest (RF) models were constructed. Model performance was assessed on internal and independent external cohorts.</div></div><div><h3>Results</h3><div>In the internal validation, the PET and combined PET/CT radiomic models outperformed the CT-alone models, with the LDA and LR classifiers achieving area under the ROC curve (AUC) greater than 0.97. In the external validation, only the models based on PET features maintained good predictive performance (LR AUC 0.8438, accuracy 81.25 %; LDA AUC 0.8281, accuracy 87.5 %). Models built on CT or combined PET/CT features failed to produce valid results, defaulting to single-class predictions. PET feature-based models demonstrated stable generalizability across datasets.</div></div><div><h3>Conclusions</h3><div>Radiomic models based on PET features and LDA or LR classifiers can accurately predict tumor invasion depth in patients with volume-equivalent ESCC and show strong external generalizability. CT or combined feature models may not be reliable under stringent tumor volume constraints.</div></div>\",\"PeriodicalId\":10624,\"journal\":{\"name\":\"Computer methods and programs in biomedicine\",\"volume\":\"271 \",\"pages\":\"Article 108988\"},\"PeriodicalIF\":4.8000,\"publicationDate\":\"2025-07-24\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Computer methods and programs in biomedicine\",\"FirstCategoryId\":\"5\",\"ListUrlMain\":\"https://www.sciencedirect.com/science/article/pii/S0169260725004055\",\"RegionNum\":2,\"RegionCategory\":\"医学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q1\",\"JCRName\":\"COMPUTER SCIENCE, INTERDISCIPLINARY APPLICATIONS\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Computer methods and programs in biomedicine","FirstCategoryId":"5","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S0169260725004055","RegionNum":2,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"COMPUTER SCIENCE, INTERDISCIPLINARY APPLICATIONS","Score":null,"Total":0}
Prediction of T2/T3 Staging in Patients with Volume-Equivalent Esophageal Squamous Cell Carcinoma on the Basis of PET/CT Radiomics
Objectives
To develop and externally validate PET/CT-based radiomic models for predicting tumor invasion depth (≤T2 vs. ≥T3) in patients with esophageal squamous cell carcinoma (ESCC) with volume-matched tumors.
Methods
Semiautomatic segmentation was performed on 18F-FDG PET images, and radiomic features were extracted from PET and coregistered CT scans. Feature reproducibility was evaluated with the intraclass correlation coefficient (ICC), which showed excellent agreement (ICC > 0.95). Propensity score matching (PSM) was applied to control for tumor volume and patient demographics. Dimensionality reduction was conducted using principal component analysis (PCA), followed by feature selection via LASSO and MRMR. Logistic regression (LR), linear discriminant analysis (LDA), support vector machine (SVM), and random forest (RF) models were constructed. Model performance was assessed on internal and independent external cohorts.
Results
In the internal validation, the PET and combined PET/CT radiomic models outperformed the CT-alone models, with the LDA and LR classifiers achieving area under the ROC curve (AUC) greater than 0.97. In the external validation, only the models based on PET features maintained good predictive performance (LR AUC 0.8438, accuracy 81.25 %; LDA AUC 0.8281, accuracy 87.5 %). Models built on CT or combined PET/CT features failed to produce valid results, defaulting to single-class predictions. PET feature-based models demonstrated stable generalizability across datasets.
Conclusions
Radiomic models based on PET features and LDA or LR classifiers can accurately predict tumor invasion depth in patients with volume-equivalent ESCC and show strong external generalizability. CT or combined feature models may not be reliable under stringent tumor volume constraints.
期刊介绍:
To encourage the development of formal computing methods, and their application in biomedical research and medical practice, by illustration of fundamental principles in biomedical informatics research; to stimulate basic research into application software design; to report the state of research of biomedical information processing projects; to report new computer methodologies applied in biomedical areas; the eventual distribution of demonstrable software to avoid duplication of effort; to provide a forum for discussion and improvement of existing software; to optimize contact between national organizations and regional user groups by promoting an international exchange of information on formal methods, standards and software in biomedicine.
Computer Methods and Programs in Biomedicine covers computing methodology and software systems derived from computing science for implementation in all aspects of biomedical research and medical practice. It is designed to serve: biochemists; biologists; geneticists; immunologists; neuroscientists; pharmacologists; toxicologists; clinicians; epidemiologists; psychiatrists; psychologists; cardiologists; chemists; (radio)physicists; computer scientists; programmers and systems analysts; biomedical, clinical, electrical and other engineers; teachers of medical informatics and users of educational software.