Clinical and molecular correlates of tumor aneuploidy in metastatic non-small cell lung cancer

Recent studies have linked elevated tumor aneuploidy to anti-tumor immune suppression and adverse survival following immunotherapy. Herein, we provide supportive evidence for tumor aneuploidy as a biomarker of response to immunotherapy in patients with non-small cell lung cancer (NSCLC). We identify a dose-response relationship between aneuploidy score and patient outcomes. In two independent NSCLC cohorts (n = 659 patients), we demonstrate a novel association between elevated aneuploidy and non-smoking-associated oncogenic driver mutations. Lastly, we report enrichment of TERT amplification and immune-suppressive phenotypes of highly aneuploid NSCLC. Taken together, our findings emphasize a potentially critical role for tumor aneuploidy in guiding immunotherapy treatment strategies.

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Publication Details

Journal
Scientific Reports
Published
2024-08-21
DOI
https://doi.org/10.1038/s41598-024-66062-5
Citations
4
Primary Topic
Lung Cancer Treatments and Mutations
Type
article
Field-Weighted Citation Impact
1.68

Funders

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article

Clinical and molecular correlates of tumor aneuploidy in metastatic non-small cell lung cancer

Sean P. Pitroda, Liam F. Spurr
4 citations
Scientific Reports
Lung Cancer Treatments and Mutations
1.68
article

Clinical and molecular correlates of tumor aneuploidy in metastatic non-small cell lung cancer

Sean P. Pitroda, Liam F. Spurr
article en
4 citations

Abstract

Recent studies have linked elevated tumor aneuploidy to anti-tumor immune suppression and adverse survival following immunotherapy. Herein, we provide supportive evidence for tumor aneuploidy as a biomarker of response to immunotherapy in patients with non-small cell lung cancer (NSCLC). We identify a dose-response relationship between aneuploidy score and patient outcomes. In two independent NSCLC cohorts (n = 659 patients), we demonstrate a novel association between elevated aneuploidy and non-smoking-associated oncogenic driver mutations. Lastly, we report enrichment of TERT amplification and immune-suppressive phenotypes of highly aneuploid NSCLC. Taken together, our findings emphasize a potentially critical role for tumor aneuploidy in guiding immunotherapy treatment strategies.

Scientific ReportsVol. 14(1)
University of Chicago (US)
LUNGevity Foundation, American Lung Association, Dr. Ralph and Marian Falk Medical Research Trust, Ludwig Institute for Cancer Research, Pritzker School of Medicine
Good health and well-being
Openalex Percentile: Top 15%
Lung Cancer Treatments and Mutations
1.68
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