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Differentiation between immune checkpoint inhibitor‐related and radiation pneumonitis in lung cancer by CT radiomics and machine learning
PURPOSE: Consolidation immunotherapy after completion of chemoradiotherapy has become the standard of care for unresectable locally advanced non‐small cell lung cancer and can induce potentially severe and life‐threatening adverse events, including both immune checkpoint inhibitor‐related pneumoniti...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9306809/ https://www.ncbi.nlm.nih.gov/pubmed/35026041 http://dx.doi.org/10.1002/mp.15451 |
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author | Cheng, Jun Pan, Yi Huang, Wei Huang, Kun Cui, Yanhai Hong, Wenhui Wang, Lingling Ni, Dong Tan, Peixin |
author_facet | Cheng, Jun Pan, Yi Huang, Wei Huang, Kun Cui, Yanhai Hong, Wenhui Wang, Lingling Ni, Dong Tan, Peixin |
author_sort | Cheng, Jun |
collection | PubMed |
description | PURPOSE: Consolidation immunotherapy after completion of chemoradiotherapy has become the standard of care for unresectable locally advanced non‐small cell lung cancer and can induce potentially severe and life‐threatening adverse events, including both immune checkpoint inhibitor‐related pneumonitis (CIP) and radiation pneumonitis (RP), which are very challenging for radiologists to diagnose. Differentiating between CIP and RP has significant implications for clinical management such as the treatments for pneumonitis and the decision to continue or restart immunotherapy. The purpose of this study is to differentiate between CIP and RP by a CT radiomics approach. METHODS: We retrospectively collected the CT images and clinical information of patients with pneumonitis who received immune checkpoint inhibitor (ICI) only (n = 28), radiotherapy (RT) only (n = 31), and ICI+RT (n = 14). Three kinds of radiomic features (intensity histogram, gray‐level co‐occurrence matrix [GLCM] based, and bag‐of‐words [BoW] features) were extracted from CT images, which characterize tissue texture at different scales. Classification models, including logistic regression, random forest, and linear SVM, were first developed and tested in patients who received ICI or RT only with 10‐fold cross‐validation and further tested in patients who received ICI+RT using clinicians’ diagnosis as a reference. RESULTS: Using 10‐fold cross‐validation, the classification models built on the intensity histogram features, GLCM‐based features, and BoW features achieved an area under curve (AUC) of 0.765, 0.848, and 0.937, respectively. The best model was then applied to the patients receiving combination treatment, achieving an AUC of 0.896. CONCLUSIONS: This study demonstrates the promising potential of radiomic analysis of CT images for differentiating between CIP and RP in lung cancer, which could be a useful tool to attribute the cause of pneumonitis in patients who receive both ICI and RT. |
format | Online Article Text |
id | pubmed-9306809 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-93068092022-07-28 Differentiation between immune checkpoint inhibitor‐related and radiation pneumonitis in lung cancer by CT radiomics and machine learning Cheng, Jun Pan, Yi Huang, Wei Huang, Kun Cui, Yanhai Hong, Wenhui Wang, Lingling Ni, Dong Tan, Peixin Med Phys QUANTITATIVE IMAGING AND IMAGE PROCESSING PURPOSE: Consolidation immunotherapy after completion of chemoradiotherapy has become the standard of care for unresectable locally advanced non‐small cell lung cancer and can induce potentially severe and life‐threatening adverse events, including both immune checkpoint inhibitor‐related pneumonitis (CIP) and radiation pneumonitis (RP), which are very challenging for radiologists to diagnose. Differentiating between CIP and RP has significant implications for clinical management such as the treatments for pneumonitis and the decision to continue or restart immunotherapy. The purpose of this study is to differentiate between CIP and RP by a CT radiomics approach. METHODS: We retrospectively collected the CT images and clinical information of patients with pneumonitis who received immune checkpoint inhibitor (ICI) only (n = 28), radiotherapy (RT) only (n = 31), and ICI+RT (n = 14). Three kinds of radiomic features (intensity histogram, gray‐level co‐occurrence matrix [GLCM] based, and bag‐of‐words [BoW] features) were extracted from CT images, which characterize tissue texture at different scales. Classification models, including logistic regression, random forest, and linear SVM, were first developed and tested in patients who received ICI or RT only with 10‐fold cross‐validation and further tested in patients who received ICI+RT using clinicians’ diagnosis as a reference. RESULTS: Using 10‐fold cross‐validation, the classification models built on the intensity histogram features, GLCM‐based features, and BoW features achieved an area under curve (AUC) of 0.765, 0.848, and 0.937, respectively. The best model was then applied to the patients receiving combination treatment, achieving an AUC of 0.896. CONCLUSIONS: This study demonstrates the promising potential of radiomic analysis of CT images for differentiating between CIP and RP in lung cancer, which could be a useful tool to attribute the cause of pneumonitis in patients who receive both ICI and RT. John Wiley and Sons Inc. 2022-01-27 2022-03 /pmc/articles/PMC9306809/ /pubmed/35026041 http://dx.doi.org/10.1002/mp.15451 Text en © 2022 The Authors. Medical Physics published by Wiley Periodicals LLC on behalf of American Association of Physicists in Medicine https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc-nd/4.0/ (https://creativecommons.org/licenses/by-nc-nd/4.0/) License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non‐commercial and no modifications or adaptations are made. |
spellingShingle | QUANTITATIVE IMAGING AND IMAGE PROCESSING Cheng, Jun Pan, Yi Huang, Wei Huang, Kun Cui, Yanhai Hong, Wenhui Wang, Lingling Ni, Dong Tan, Peixin Differentiation between immune checkpoint inhibitor‐related and radiation pneumonitis in lung cancer by CT radiomics and machine learning |
title | Differentiation between immune checkpoint inhibitor‐related and radiation pneumonitis in lung cancer by CT radiomics and machine learning |
title_full | Differentiation between immune checkpoint inhibitor‐related and radiation pneumonitis in lung cancer by CT radiomics and machine learning |
title_fullStr | Differentiation between immune checkpoint inhibitor‐related and radiation pneumonitis in lung cancer by CT radiomics and machine learning |
title_full_unstemmed | Differentiation between immune checkpoint inhibitor‐related and radiation pneumonitis in lung cancer by CT radiomics and machine learning |
title_short | Differentiation between immune checkpoint inhibitor‐related and radiation pneumonitis in lung cancer by CT radiomics and machine learning |
title_sort | differentiation between immune checkpoint inhibitor‐related and radiation pneumonitis in lung cancer by ct radiomics and machine learning |
topic | QUANTITATIVE IMAGING AND IMAGE PROCESSING |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9306809/ https://www.ncbi.nlm.nih.gov/pubmed/35026041 http://dx.doi.org/10.1002/mp.15451 |
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