Novel radiogenomics approach to predict and characterize pneumonitis in stage III NSCLC

Unresectable stage III NSCLC is now treated with chemoradiation (CRT) followed by immune checkpoint inhibitors (ICI). Pneumonitis, a common CRT complication, has heightened risk with ICI, potentially causing severe outcomes. Currently, there are no biomarkers to predict pneumonitis risk or differentiate between radiation-induced pneumonitis (RTP) and ICI-induced pneumonitis (IIP). This study analyzed 293 patients from two institutions, with 140 experiencing pneumonitis (RTP: 84, IIP: 56). Two models were developed: M1 predicted pneumonitis risk using seven radiomic features, achieving high accuracy across internal and external datasets (AUCs: 0.76 and 0.85). M2 differentiated RTP from IIP, with strong performance (AUCs: 0.86 and 0.81). Gene set enrichment analysis linked high pneumonitis risk to pathways such as ECM-receptor interaction and T-cell signaling, while high IIP risk correlated with MAPK and JAK-STAT pathways. Radiomic models show promise in early pneumonitis risk stratification and distinguishing pneumonitis types, potentially guiding personalized NSCLC treatment.

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Publication Details

Journal
npj Precision Oncology
Published
2024-12-24
DOI
https://doi.org/10.1038/s41698-024-00790-9
Citations
10
Primary Topic
Radiomics and Machine Learning in Medical Imaging
Type
article
Field-Weighted Citation Impact
4.04

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article

Novel radiogenomics approach to predict and characterize pneumonitis in stage III NSCLC

Nathan A. Pennell, Anant Madabhushi, Pradnya D. Patil, Mohammadhadi Khorrami et al.
10 citations
npj Precision Oncology
Radiomics and Machine Learning in Medical Imaging
4.04
article

Novel radiogenomics approach to predict and characterize pneumonitis in stage III NSCLC

Nathan A. Pennell, Anant Madabhushi, Pradnya D. Patil, Mohammadhadi Khorrami, Lukas Delasos, Amit Banwari Gupta, Khalid Jazieh, Kevin L. Stephans, Kristin Ann Higgins, Yifu Ding, Vidya Sankar Viswanathan, Pushkar Mutha
article en
10 citations

Abstract

Unresectable stage III NSCLC is now treated with chemoradiation (CRT) followed by immune checkpoint inhibitors (ICI). Pneumonitis, a common CRT complication, has heightened risk with ICI, potentially causing severe outcomes. Currently, there are no biomarkers to predict pneumonitis risk or differentiate between radiation-induced pneumonitis (RTP) and ICI-induced pneumonitis (IIP). This study analyzed 293 patients from two institutions, with 140 experiencing pneumonitis (RTP: 84, IIP: 56). Two models were developed: M1 predicted pneumonitis risk using seven radiomic features, achieving high accuracy across internal and external datasets (AUCs: 0.76 and 0.85). M2 differentiated RTP from IIP, with strong performance (AUCs: 0.86 and 0.81). Gene set enrichment analysis linked high pneumonitis risk to pathways such as ECM-receptor interaction and T-cell signaling, while high IIP risk correlated with MAPK and JAK-STAT pathways. Radiomic models show promise in early pneumonitis risk stratification and distinguishing pneumonitis types, potentially guiding personalized NSCLC treatment.

npj Precision OncologyVol. 8(1)
Georgia Institute of Technology (US), Cleveland Clinic (US), Emory University (US), University Hospitals of Cleveland (US), Veterans Health Administration (US), Atlanta VA Medical Center (US), Covance (United States) (US)
U.S. Department of Defense, Foundation for the National Institutes of Health, U.S. Department of Veterans Affairs, Eli Lilly and Company, AstraZeneca, California Breast Cancer Research Program, National Institutes of Health, National Heart, Lung, and Blood Institute, National Cancer Institute, National Institute of Biomedical Imaging and Bioengineering, National Center for Research Resources, DOD Prostate Cancer Research Program, DOD Peer Reviewed Cancer Research Program
Openalex Percentile: Top 6%
Radiomics and Machine Learning in Medical Imaging
4.04
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