Development and validation a radiomics combined clinical model predicts treatment response for esophageal squamous cell carcinoma patients

Abstract Purpose This study is aimed to develop and validate a machine learning model, which combined radiomics and clinical characteristics to predicting the definitive chemoradiotherapy (dCRT) treatment response in esophageal squamous cell carcinoma (ESCC) patients. Methods: 204 advanced ESCC pati...

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Main Authors: Xiaoyan Yin, Yongbin Cui, Tonghai Liu, Zhenjiang Li, Huiling Liu, Xingmin Ma, Xue Sha, Changsheng Ma, Dali Han, Yong Yin
Format: Article
Language:English
Published: BMC 2025-04-01
Series:BMC Gastroenterology
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Online Access:https://doi.org/10.1186/s12876-025-03899-8
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author Xiaoyan Yin
Yongbin Cui
Tonghai Liu
Zhenjiang Li
Huiling Liu
Xingmin Ma
Xue Sha
Changsheng Ma
Dali Han
Yong Yin
author_facet Xiaoyan Yin
Yongbin Cui
Tonghai Liu
Zhenjiang Li
Huiling Liu
Xingmin Ma
Xue Sha
Changsheng Ma
Dali Han
Yong Yin
author_sort Xiaoyan Yin
collection DOAJ
description Abstract Purpose This study is aimed to develop and validate a machine learning model, which combined radiomics and clinical characteristics to predicting the definitive chemoradiotherapy (dCRT) treatment response in esophageal squamous cell carcinoma (ESCC) patients. Methods: 204 advanced ESCC patients were included who underwent dCRT at our hospital. Patients were randomly divided into training cohort and validation cohort with a ratio of 7:3. The radiomics features were selected by LASSO algorithm. The clinical features were selected by multivariate logistics analysis (p < 0.05). Subsequently, a combined radiomics and clinical model was established and validated to predict the treatment response in ESCC patients by logistic regression model. The performance of the model was evaluated by receiver operating characteristic (ROC) curve, decision curve analysis (DCA), nomogram, and calibration curve. Results: Total of 944 radiomics features were extracted from the pre-treatment contrasted enhanced CT images (CECT). After feature selection, 3 radiomics features and 3 clinical features were identified as the most predictive variables. The combined model shows better prediction performance among radiomics model or clinical model. The radiomics model’s AUC values in training and validation cohort are 0.71,0.69. As for clinical model the AUC values were 0.74,0.75 in training and validation cohort. However, the AUC values in combined model are 0.79, 0.78 in training cohort and validation cohort, respectively. DCA and calibration curve also demonstrated good performance for the combined model. Conclusion: The radiomics combined clinical features model demonstrates superior treatment response prediction ability for ESCC patients received dCRT. This model has the potential to assist clinicians in identifying non-responsive patients before treatment and guide individualized therapy for advanced ESCC patients.
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spelling doaj-art-355c5e2f7d5348e6bac24501453d167c2025-08-20T02:10:50ZengBMCBMC Gastroenterology1471-230X2025-04-012511910.1186/s12876-025-03899-8Development and validation a radiomics combined clinical model predicts treatment response for esophageal squamous cell carcinoma patientsXiaoyan Yin0Yongbin Cui1Tonghai Liu2Zhenjiang Li3Huiling Liu4Xingmin Ma5Xue Sha6Changsheng Ma7Dali Han8Yong Yin9Department of Radiation Oncology, Shandong Cancer Hospital and Institute, Shandong First Medical University, Shandong Academy of Medical SciencesDepartment of Radiation Oncology, Shandong Cancer Hospital and Institute, Shandong First Medical University, Shandong Academy of Medical SciencesDepartment of Radiation Oncology, Shandong Cancer Hospital and Institute, Shandong First Medical University, Shandong Academy of Medical SciencesDepartment of Radiation Oncology, Shandong Cancer Hospital and Institute, Shandong First Medical University, Shandong Academy of Medical SciencesDepartment of Radiation Oncology, Affiliated Cancer Hospital, The Third Affiliated Teaching Hospital of Xinjiang Medical UniversityDepartment of Radiation Oncology, Shandong Cancer Hospital and Institute, Shandong First Medical University, Shandong Academy of Medical SciencesDepartment of Radiation Oncology, Affiliated Cancer Hospital, The Third Affiliated Teaching Hospital of Xinjiang Medical UniversityDepartment of Radiation Oncology, Shandong Cancer Hospital and Institute, Shandong First Medical University, Shandong Academy of Medical SciencesDepartment of Radiation Oncology, Shandong Cancer Hospital and Institute, Shandong First Medical University, Shandong Academy of Medical SciencesDepartment of Radiation Oncology, Shandong Cancer Hospital and Institute, Shandong First Medical University, Shandong Academy of Medical SciencesAbstract Purpose This study is aimed to develop and validate a machine learning model, which combined radiomics and clinical characteristics to predicting the definitive chemoradiotherapy (dCRT) treatment response in esophageal squamous cell carcinoma (ESCC) patients. Methods: 204 advanced ESCC patients were included who underwent dCRT at our hospital. Patients were randomly divided into training cohort and validation cohort with a ratio of 7:3. The radiomics features were selected by LASSO algorithm. The clinical features were selected by multivariate logistics analysis (p < 0.05). Subsequently, a combined radiomics and clinical model was established and validated to predict the treatment response in ESCC patients by logistic regression model. The performance of the model was evaluated by receiver operating characteristic (ROC) curve, decision curve analysis (DCA), nomogram, and calibration curve. Results: Total of 944 radiomics features were extracted from the pre-treatment contrasted enhanced CT images (CECT). After feature selection, 3 radiomics features and 3 clinical features were identified as the most predictive variables. The combined model shows better prediction performance among radiomics model or clinical model. The radiomics model’s AUC values in training and validation cohort are 0.71,0.69. As for clinical model the AUC values were 0.74,0.75 in training and validation cohort. However, the AUC values in combined model are 0.79, 0.78 in training cohort and validation cohort, respectively. DCA and calibration curve also demonstrated good performance for the combined model. Conclusion: The radiomics combined clinical features model demonstrates superior treatment response prediction ability for ESCC patients received dCRT. This model has the potential to assist clinicians in identifying non-responsive patients before treatment and guide individualized therapy for advanced ESCC patients.https://doi.org/10.1186/s12876-025-03899-8RadiomicsTreatment responseDefinitive chemoradiotherapyEsophageal squamous cell carcinoma
spellingShingle Xiaoyan Yin
Yongbin Cui
Tonghai Liu
Zhenjiang Li
Huiling Liu
Xingmin Ma
Xue Sha
Changsheng Ma
Dali Han
Yong Yin
Development and validation a radiomics combined clinical model predicts treatment response for esophageal squamous cell carcinoma patients
BMC Gastroenterology
Radiomics
Treatment response
Definitive chemoradiotherapy
Esophageal squamous cell carcinoma
title Development and validation a radiomics combined clinical model predicts treatment response for esophageal squamous cell carcinoma patients
title_full Development and validation a radiomics combined clinical model predicts treatment response for esophageal squamous cell carcinoma patients
title_fullStr Development and validation a radiomics combined clinical model predicts treatment response for esophageal squamous cell carcinoma patients
title_full_unstemmed Development and validation a radiomics combined clinical model predicts treatment response for esophageal squamous cell carcinoma patients
title_short Development and validation a radiomics combined clinical model predicts treatment response for esophageal squamous cell carcinoma patients
title_sort development and validation a radiomics combined clinical model predicts treatment response for esophageal squamous cell carcinoma patients
topic Radiomics
Treatment response
Definitive chemoradiotherapy
Esophageal squamous cell carcinoma
url https://doi.org/10.1186/s12876-025-03899-8
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