Quantification of preexisting lung ground glass opacities on CT for predicting checkpoint inhibitor pneumonitis in advanced non-small cell lung cancer patients

Abstract Background Immune checkpoint inhibitors (ICIs) can lead to life-threatening pneumonitis, and pre-existing interstitial lung abnormalities (ILAs) are a risk factor for checkpoint inhibitor pneumonitis (CIP). However, the subjective assessment of ILA and the lack of standardized methods restr...

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Main Authors: Xinyue Wang, Jinkun Zhao, Ting Mei, Wenting Liu, Xiuqiong Chen, Jingya Wang, Richeng Jiang, Zhaoxiang Ye, Dingzhi Huang
Format: Article
Language:English
Published: BMC 2024-02-01
Series:BMC Cancer
Subjects:
Online Access:https://doi.org/10.1186/s12885-024-12008-z
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author Xinyue Wang
Jinkun Zhao
Ting Mei
Wenting Liu
Xiuqiong Chen
Jingya Wang
Richeng Jiang
Zhaoxiang Ye
Dingzhi Huang
author_facet Xinyue Wang
Jinkun Zhao
Ting Mei
Wenting Liu
Xiuqiong Chen
Jingya Wang
Richeng Jiang
Zhaoxiang Ye
Dingzhi Huang
author_sort Xinyue Wang
collection DOAJ
description Abstract Background Immune checkpoint inhibitors (ICIs) can lead to life-threatening pneumonitis, and pre-existing interstitial lung abnormalities (ILAs) are a risk factor for checkpoint inhibitor pneumonitis (CIP). However, the subjective assessment of ILA and the lack of standardized methods restrict its clinical utility as a predictive factor. This study aims to identify non-small cell lung cancer (NSCLC) patients at high risk of CIP using quantitative imaging. Methods This cohort study involved 206 cases in the training set and 111 cases in the validation set. It included locally advanced or metastatic NSCLC patients who underwent ICI therapy. A deep learning algorithm labeled the interstitial lesions and computed their volume. Two predictive models were developed to predict the probability of grade ≥ 2 CIP or severe CIP (grade ≥ 3). Cox proportional hazard models were employed to analyze predictors of progression-free survival (PFS). Results In a training cohort of 206 patients, 21.4% experienced CIP. Two models were developed to predict the probability of CIP based on different predictors. Model 1 utilized age, histology, and preexisting ground glass opacity (GGO) percentage of the whole lung to predict grade ≥ 2 CIP, while Model 2 used histology and GGO percentage in the right lower lung to predict grade ≥ 3 CIP. These models were validated, and their accuracy was assessed. In another exploratory analysis, the presence of GGOs involving more than one lobe on pretreatment CT scans was identified as a risk factor for progression-free survival. Conclusions The assessment of GGO volume and distribution on pre-treatment CT scans could assist in monitoring and manage the risk of CIP in NSCLC patients receiving ICI therapy. Clinical relevance statement This study’s quantitative imaging and computational analysis can help identify NSCLC patients at high risk of CIP, allowing for better risk management and potentially improved outcomes in those receivingICI treatment.
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spelling doaj.art-1f9d79e85c6548d99c903da4a63c15f92024-03-05T19:23:01ZengBMCBMC Cancer1471-24072024-02-0124111410.1186/s12885-024-12008-zQuantification of preexisting lung ground glass opacities on CT for predicting checkpoint inhibitor pneumonitis in advanced non-small cell lung cancer patientsXinyue Wang0Jinkun Zhao1Ting Mei2Wenting Liu3Xiuqiong Chen4Jingya Wang5Richeng Jiang6Zhaoxiang Ye7Dingzhi Huang8Tianjin Medical University Cancer Institute & Hospital, National Clinical Research Center for CancerTianjin Medical University Cancer Institute & Hospital, National Clinical Research Center for CancerTianjin Medical University Cancer Institute & Hospital, National Clinical Research Center for CancerTianjin Medical University Cancer Institute & Hospital, National Clinical Research Center for CancerTianjin Medical University Cancer Institute & Hospital, National Clinical Research Center for CancerTianjin Medical University Cancer Institute & Hospital, National Clinical Research Center for CancerTianjin Medical University Cancer Institute & Hospital, National Clinical Research Center for CancerTianjin Medical University Cancer Institute & Hospital, National Clinical Research Center for CancerTianjin Medical University Cancer Institute & Hospital, National Clinical Research Center for CancerAbstract Background Immune checkpoint inhibitors (ICIs) can lead to life-threatening pneumonitis, and pre-existing interstitial lung abnormalities (ILAs) are a risk factor for checkpoint inhibitor pneumonitis (CIP). However, the subjective assessment of ILA and the lack of standardized methods restrict its clinical utility as a predictive factor. This study aims to identify non-small cell lung cancer (NSCLC) patients at high risk of CIP using quantitative imaging. Methods This cohort study involved 206 cases in the training set and 111 cases in the validation set. It included locally advanced or metastatic NSCLC patients who underwent ICI therapy. A deep learning algorithm labeled the interstitial lesions and computed their volume. Two predictive models were developed to predict the probability of grade ≥ 2 CIP or severe CIP (grade ≥ 3). Cox proportional hazard models were employed to analyze predictors of progression-free survival (PFS). Results In a training cohort of 206 patients, 21.4% experienced CIP. Two models were developed to predict the probability of CIP based on different predictors. Model 1 utilized age, histology, and preexisting ground glass opacity (GGO) percentage of the whole lung to predict grade ≥ 2 CIP, while Model 2 used histology and GGO percentage in the right lower lung to predict grade ≥ 3 CIP. These models were validated, and their accuracy was assessed. In another exploratory analysis, the presence of GGOs involving more than one lobe on pretreatment CT scans was identified as a risk factor for progression-free survival. Conclusions The assessment of GGO volume and distribution on pre-treatment CT scans could assist in monitoring and manage the risk of CIP in NSCLC patients receiving ICI therapy. Clinical relevance statement This study’s quantitative imaging and computational analysis can help identify NSCLC patients at high risk of CIP, allowing for better risk management and potentially improved outcomes in those receivingICI treatment.https://doi.org/10.1186/s12885-024-12008-zNon-small cell lung cancerImmune checkpoint inhibitorCheckpoint inhibitor pneumonitisGround glass opacityDeep learning
spellingShingle Xinyue Wang
Jinkun Zhao
Ting Mei
Wenting Liu
Xiuqiong Chen
Jingya Wang
Richeng Jiang
Zhaoxiang Ye
Dingzhi Huang
Quantification of preexisting lung ground glass opacities on CT for predicting checkpoint inhibitor pneumonitis in advanced non-small cell lung cancer patients
BMC Cancer
Non-small cell lung cancer
Immune checkpoint inhibitor
Checkpoint inhibitor pneumonitis
Ground glass opacity
Deep learning
title Quantification of preexisting lung ground glass opacities on CT for predicting checkpoint inhibitor pneumonitis in advanced non-small cell lung cancer patients
title_full Quantification of preexisting lung ground glass opacities on CT for predicting checkpoint inhibitor pneumonitis in advanced non-small cell lung cancer patients
title_fullStr Quantification of preexisting lung ground glass opacities on CT for predicting checkpoint inhibitor pneumonitis in advanced non-small cell lung cancer patients
title_full_unstemmed Quantification of preexisting lung ground glass opacities on CT for predicting checkpoint inhibitor pneumonitis in advanced non-small cell lung cancer patients
title_short Quantification of preexisting lung ground glass opacities on CT for predicting checkpoint inhibitor pneumonitis in advanced non-small cell lung cancer patients
title_sort quantification of preexisting lung ground glass opacities on ct for predicting checkpoint inhibitor pneumonitis in advanced non small cell lung cancer patients
topic Non-small cell lung cancer
Immune checkpoint inhibitor
Checkpoint inhibitor pneumonitis
Ground glass opacity
Deep learning
url https://doi.org/10.1186/s12885-024-12008-z
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