Abstract
In early-stage non-small cell lung cancer, the combination of neoadjuvant anti-PD-L1 and subablative stereotactic body radiation therapy (SBRT) is associated with higher rates of major pathologic response compared to anti-PD-L1 alone. Here, we identify a 140-gene set, enriched in genes characteristic of highly proliferating cells, associated with response to the dual therapy. Analysis of on-treatment transcriptome data indicate roles for T and B cells in response. The 140-gene set is associated with disease-free survival when applied to the combined trial arms. This 140-gene set identifies a subclass of tumors in all 7 of The Cancer Genome Atlas tumor types examined. Worse survival is associated with the 140-gene signature in 5 of these tumor types. Collectively, our data support that this 140-gene set, discovered in association with response to combined anti-PD-L1 and SBRT, identifies a clinically aggressive subclass of solid tumors that may be more likely to respond to immunotherapies.
Original language | English (US) |
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Article number | 101438 |
Journal | Cell Reports Medicine |
Volume | 5 |
Issue number | 3 |
DOIs | |
State | Published - Mar 19 2024 |
Keywords
- biomarker immunotherapy response
- combination immunotherapy radiation
- immunotherapy
- NSCLC
- radiation therapy
- rapidly proliferating tumors
ASJC Scopus subject areas
- Biochemistry, Genetics and Molecular Biology(all)