A signature of enhanced proliferation associated with response and survival to anti-PD-L1 therapy in early-stage non-small cell lung cancer

Nasser K. Altorki, Bhavneet Bhinder, Alain C. Borczuk, Olivier Elemento, Vivek Mittal, Timothy E. McGraw

Research output: Contribution to journalArticlepeer-review

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 languageEnglish (US)
Article number101438
JournalCell Reports Medicine
Volume5
Issue number3
DOIs
StatePublished - 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)

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