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Predicting response to immunotherapy plus chemotherapy in patients with esophageal squamous cell carcinoma using non-invasive Radiomic biomarkers

OBJECTIVES: To develop and validate a radiomics model for evaluating treatment response to immune-checkpoint inhibitor plus chemotherapy (ICI + CT) in patients with advanced esophageal squamous cell carcinoma (ESCC). METHODS: A total of 64 patients with advance ESCC receiving first-line ICI + CT at...

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Autores principales: Zhu, Ying, Yao, Wang, Xu, Bing-Chen, Lei, Yi-Yan, Guo, Qi-Kun, Liu, Li-Zhi, Li, Hao-Jiang, Xu, Min, Yan, Jing, Chang, Dan-Dan, Feng, Shi-Ting, Zhu, Zhi-Hua
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8557514/
https://www.ncbi.nlm.nih.gov/pubmed/34717582
http://dx.doi.org/10.1186/s12885-021-08899-x
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author Zhu, Ying
Yao, Wang
Xu, Bing-Chen
Lei, Yi-Yan
Guo, Qi-Kun
Liu, Li-Zhi
Li, Hao-Jiang
Xu, Min
Yan, Jing
Chang, Dan-Dan
Feng, Shi-Ting
Zhu, Zhi-Hua
author_facet Zhu, Ying
Yao, Wang
Xu, Bing-Chen
Lei, Yi-Yan
Guo, Qi-Kun
Liu, Li-Zhi
Li, Hao-Jiang
Xu, Min
Yan, Jing
Chang, Dan-Dan
Feng, Shi-Ting
Zhu, Zhi-Hua
author_sort Zhu, Ying
collection PubMed
description OBJECTIVES: To develop and validate a radiomics model for evaluating treatment response to immune-checkpoint inhibitor plus chemotherapy (ICI + CT) in patients with advanced esophageal squamous cell carcinoma (ESCC). METHODS: A total of 64 patients with advance ESCC receiving first-line ICI + CT at two centers between January 2019 and June 2020 were enrolled in this study. Both 2D ROIs and 3D ROIs were segmented. ComBat correction was applied to minimize the potential bias on the results due to different scan protocols. A total of 788 features were extracted and radiomics models were built on corrected/uncorrected 2D and 3D features by using 5-fold cross-validation. The performance of the radiomics models was assessed by its discrimination, calibration and clinical usefulness with independent validation. RESULTS: Five features and support vector machine algorithm were selected to build the 2D uncorrected, 2D corrected, 3D uncorrected and 3D corrected radiomics models. The 2D radiomics models significantly outperformed the 3D radiomics models in both primary and validation cohorts. When ComBat correction was used, the performance of 2D models was better (p = 0.0059) in the training cohort, and significantly better (p < 0.0001) in the validation cohort. The 2D corrected radiomics model yielded the optimal performance and was used to build the nomogram. The calibration curve of the radiomics model demonstrated good agreement between prediction and observation and the decision curve analysis confirmed the clinical utility. CONCLUSIONS: The easy-to-use 2D corrected radiomics model could facilitate noninvasive preselection of ESCC patients who would benefit from ICI + CT. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12885-021-08899-x.
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spelling pubmed-85575142021-11-01 Predicting response to immunotherapy plus chemotherapy in patients with esophageal squamous cell carcinoma using non-invasive Radiomic biomarkers Zhu, Ying Yao, Wang Xu, Bing-Chen Lei, Yi-Yan Guo, Qi-Kun Liu, Li-Zhi Li, Hao-Jiang Xu, Min Yan, Jing Chang, Dan-Dan Feng, Shi-Ting Zhu, Zhi-Hua BMC Cancer Research OBJECTIVES: To develop and validate a radiomics model for evaluating treatment response to immune-checkpoint inhibitor plus chemotherapy (ICI + CT) in patients with advanced esophageal squamous cell carcinoma (ESCC). METHODS: A total of 64 patients with advance ESCC receiving first-line ICI + CT at two centers between January 2019 and June 2020 were enrolled in this study. Both 2D ROIs and 3D ROIs were segmented. ComBat correction was applied to minimize the potential bias on the results due to different scan protocols. A total of 788 features were extracted and radiomics models were built on corrected/uncorrected 2D and 3D features by using 5-fold cross-validation. The performance of the radiomics models was assessed by its discrimination, calibration and clinical usefulness with independent validation. RESULTS: Five features and support vector machine algorithm were selected to build the 2D uncorrected, 2D corrected, 3D uncorrected and 3D corrected radiomics models. The 2D radiomics models significantly outperformed the 3D radiomics models in both primary and validation cohorts. When ComBat correction was used, the performance of 2D models was better (p = 0.0059) in the training cohort, and significantly better (p < 0.0001) in the validation cohort. The 2D corrected radiomics model yielded the optimal performance and was used to build the nomogram. The calibration curve of the radiomics model demonstrated good agreement between prediction and observation and the decision curve analysis confirmed the clinical utility. CONCLUSIONS: The easy-to-use 2D corrected radiomics model could facilitate noninvasive preselection of ESCC patients who would benefit from ICI + CT. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12885-021-08899-x. BioMed Central 2021-10-30 /pmc/articles/PMC8557514/ /pubmed/34717582 http://dx.doi.org/10.1186/s12885-021-08899-x Text en © The Author(s) 2021 https://creativecommons.org/licenses/by/4.0/Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data.
spellingShingle Research
Zhu, Ying
Yao, Wang
Xu, Bing-Chen
Lei, Yi-Yan
Guo, Qi-Kun
Liu, Li-Zhi
Li, Hao-Jiang
Xu, Min
Yan, Jing
Chang, Dan-Dan
Feng, Shi-Ting
Zhu, Zhi-Hua
Predicting response to immunotherapy plus chemotherapy in patients with esophageal squamous cell carcinoma using non-invasive Radiomic biomarkers
title Predicting response to immunotherapy plus chemotherapy in patients with esophageal squamous cell carcinoma using non-invasive Radiomic biomarkers
title_full Predicting response to immunotherapy plus chemotherapy in patients with esophageal squamous cell carcinoma using non-invasive Radiomic biomarkers
title_fullStr Predicting response to immunotherapy plus chemotherapy in patients with esophageal squamous cell carcinoma using non-invasive Radiomic biomarkers
title_full_unstemmed Predicting response to immunotherapy plus chemotherapy in patients with esophageal squamous cell carcinoma using non-invasive Radiomic biomarkers
title_short Predicting response to immunotherapy plus chemotherapy in patients with esophageal squamous cell carcinoma using non-invasive Radiomic biomarkers
title_sort predicting response to immunotherapy plus chemotherapy in patients with esophageal squamous cell carcinoma using non-invasive radiomic biomarkers
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8557514/
https://www.ncbi.nlm.nih.gov/pubmed/34717582
http://dx.doi.org/10.1186/s12885-021-08899-x
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