Predicting Immunotherapy Outcomes in NSCLC Using RNA and Pathology from Multicenter Clinical Trials

Immune checkpoint inhibitors (ICIs) are widely used to treat advanced non-small cell lung cancer (NSCLC). However, it remains crucial to identify patients who are unlikely to benefit from immunotherapy and to explore potential combination treatment strategies. In this study, 1127 advanced NSCLC patients from multicenter randomized clinical trials (OAK, POPLAR, ORIENT-11) and an in-house cohort who received ICIs, ICIs combined with chemotherapy, or chemotherapy alone are analyzed. Using bulk RNA-seq transcriptomic data, an RNA-based model, named the Lung Cancer Immunotherapy Response Assessment (LIRA), is developed, utilizing interaction analysis and a random forest algorithm to predict immunotherapy outcomes. LIRA outperforms PD-L1 expression and tumor mutation burden in predicting responses, particularly in identifying early progression risk during ICI monotherapy (HR: 0.15, 95% CI: 0.11-0.20). Tumor profile analysis reveals that LRP8 and HDAC4 are associated with immunotherapy outcomes. Additionally, scRNA-seq analysis of NSCLC tumors indicates a higher prevalence of T cells and a reduced proportion of epithelial cells in samples with a high LIRA-score. The deep learning model pinpointed critical high-attention regions within whole-slide images that contributed decisively to the LIRA predictions. In summary, these results demonstrate that LIRA enables independent risk stratification of NSCLC patients and provides insights into potential resistance mechanisms.

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Publication Details

Journal
Advanced Science
Published
2025-10-29
DOI
https://doi.org/10.1002/advs.202502037
Primary Topic
Cancer Immunotherapy and Biomarkers
Type
article
Field-Weighted Citation Impact
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article

Predicting Immunotherapy Outcomes in NSCLC Using RNA and Pathology from Multicenter Clinical Trials

Dongqiang Zeng, Na Huang, Rong Hua Guo, Jianping Bin et al.
Advanced Science
Cancer Immunotherapy and Biomarkers
article

Predicting Immunotherapy Outcomes in NSCLC Using RNA and Pathology from Multicenter Clinical Trials

Dongqiang Zeng, Na Huang, Rong Hua Guo, Jianping Bin, Zuqiang Wu, Xiansheng Lu, Yulin Liao, Wenchao Gu, Wangjun Liao, Peng Luo, Luyang Jiang, Gang Chen, Min Shi, Wenjun Qiu, Xiaoxiang Rong, Jiani Wu, Yunfang Yu, Huiying Sun, Yonggang Liu, Lingling Wang, Yuanyuan Wang, Zhaojun Wang, Rui Zhou, Shao-wei Li, Yiran Fang, Qianqian Mao, Jianhua Wu, Zhenhua Huang, Ji-Guang Wang, Xiatong Huang, Siting Zheng, Guichuang Ma, Gaofeng Wang
article en

Abstract

Immune checkpoint inhibitors (ICIs) are widely used to treat advanced non-small cell lung cancer (NSCLC). However, it remains crucial to identify patients who are unlikely to benefit from immunotherapy and to explore potential combination treatment strategies. In this study, 1127 advanced NSCLC patients from multicenter randomized clinical trials (OAK, POPLAR, ORIENT-11) and an in-house cohort who received ICIs, ICIs combined with chemotherapy, or chemotherapy alone are analyzed. Using bulk RNA-seq transcriptomic data, an RNA-based model, named the Lung Cancer Immunotherapy Response Assessment (LIRA), is developed, utilizing interaction analysis and a random forest algorithm to predict immunotherapy outcomes. LIRA outperforms PD-L1 expression and tumor mutation burden in predicting responses, particularly in identifying early progression risk during ICI monotherapy (HR: 0.15, 95% CI: 0.11-0.20). Tumor profile analysis reveals that LRP8 and HDAC4 are associated with immunotherapy outcomes. Additionally, scRNA-seq analysis of NSCLC tumors indicates a higher prevalence of T cells and a reduced proportion of epithelial cells in samples with a high LIRA-score. The deep learning model pinpointed critical high-attention regions within whole-slide images that contributed decisively to the LIRA predictions. In summary, these results demonstrate that LIRA enables independent risk stratification of NSCLC patients and provides insights into potential resistance mechanisms.

Advanced ScienceVol. 13(3)
Macau University of Science and Technology (MO), Johns Hopkins University (US), Foshan University (CN), Sun Yat-sen University (CN), Chiba University (JP), Johns Hopkins Medicine (US), Sun Yat-sen Memorial Hospital (CN), The First People's Hospital of Shunde (CN), Nanfang Hospital (CN), Foshan Hospital of TCM (CN), Zhujiang Hospital (CN), Sun Yat-sen University Cancer Center (CN), Southern Medical University (CN), University of Hong Kong (HK), South China University of Technology (CN)
Openalex Percentile: Top 58%
Cancer Immunotherapy and Biomarkers
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