Divergent Clinical and Immunologic Outcomes Based on <i>STK11</i> Co-mutation Status in Resectable <i>KRAS-</i> Mutant Lung Cancers Following Neoadjuvant Immune Checkpoint Blockade

These divergent T-cell transcriptional fates suggest that T-cell maintenance and residence may be detrimental to antitumor immunity in the context of neoadjuvant ICB for resectable NSCLC, regardless of KRAS mutation status. Our work provides a basis for future investigations into the mechanisms underpinning prostaglandin E2 signaling and IL-2 signaling as they relate to T-cell immunity to cancer and to divergent clinical outcomes in KRASmut/STK11mut NSCLC treated with neoadjuvant ICB.

Authors

Institutions

Publication Details

Journal
Clinical Cancer Research
Published
2024-11-15
DOI
https://doi.org/10.1158/1078-0432.ccr-24-2983
Citations
9
Primary Topic
Cancer Immunotherapy and Biomarkers
Type
article
Field-Weighted Citation Impact
2.54

Funders

Controls
|||
ALL TIME
JAN
FEB
MAR
APR
MAY
JUN
JUL
AUG
SEP
OCT
article

Divergent Clinical and Immunologic Outcomes Based on STK11 Co-mutation Status in Resectable KRAS- Mutant Lung Cancers Following Neoadjuvant Immune Checkpoint Blockade

Zhen Zeng, Samuel Rosner, Lavanya Sivapalan, Rohit Thummalapalli et al.
9 citations
Clinical Cancer Research
Cancer Immunotherapy and Biomarkers
2.54
article

Divergent Clinical and Immunologic Outcomes Based on STK11 Co-mutation Status in Resectable KRAS- Mutant Lung Cancers Following Neoadjuvant Immune Checkpoint Blockade

Zhen Zeng, Samuel Rosner, Lavanya Sivapalan, Rohit Thummalapalli, Brad Presson, Julie R. Brahmer, Hongkai Ji, Stephen Broderick, Gavin Pereira, Janis M. Taube, Sydney Connor, Joshua E. Reuss, Jonathan Spicer, Khaled Sanber, Valsamo Anagnostou, Kristen Ashley Marrone, Patrick M. Forde, Marianna Zahurak, David R. Jones, Drew M. Pardoll, Julie S. Deutsch, Tricia R. Cottrell, Zhicheng Ji, Kellie N. Smith, Roni Rayes, Jamie E. Chaft, Tianbei Zhang, Dipika Singh, Isha Gurumurthy
article en
9 citations

Abstract

These divergent T-cell transcriptional fates suggest that T-cell maintenance and residence may be detrimental to antitumor immunity in the context of neoadjuvant ICB for resectable NSCLC, regardless of KRAS mutation status. Our work provides a basis for future investigations into the mechanisms underpinning prostaglandin E2 signaling and IL-2 signaling as they relate to T-cell immunity to cancer and to divergent clinical outcomes in KRASmut/STK11mut NSCLC treated with neoadjuvant ICB.

Clinical Cancer ResearchVol. 31(2)
University of Maryland, Baltimore (US), University of Maryland Medical Center (US), Memorial Sloan Kettering Cancer Center (US), The University of Texas MD Anderson Cancer Center (US), Johns Hopkins University (US), Duke University (US), Georgetown University (US), Queen's University (CA), Cornell University (US), Johns Hopkins Medicine (US), Georgetown University Medical Center (US), McGill University Health Centre (CA), Queens University (BD), Sidney Kimmel Cancer Center (US), Vince Lombardi Cancer Clinic (US), Sidney Kimmel Comprehensive Cancer Center (US), McGill University (CA)
Conquer Cancer Foundation, LUNGevity Foundation, Bristol-Myers Squibb, Mark Foundation For Cancer Research, Swim Across America, National Institutes of Health
Good health and well-being
Openalex Percentile: Top 8%
Cancer Immunotherapy and Biomarkers
2.54
AI Navigator

Ask Laika to Summarize, Analyze, and Connect papers live on the map.

Summarize Papers & Methodologies

Extract key findings, datasets, and comparative methods across publications.

Benchmark Rankings & Visual Analytics

Rank top research institutions, authors, funders, topics, and journals by Field-Weighted Citation Impact (FWCI) and paper volume with instant charts.

Connect Distant Disciplines

Bridge topological clusters on the map to find hidden collaborative intersections.