Abstract 6469: Longitudinal loss of microbiome stability is associated with poor response to immune checkpoint inhibitors in lung cancer and melanoma

Abstract While immune checkpoint inhibitors (ICI)-based regimens and chemo-immunotherapy combinations (chemo-ICI) are now first-line therapy for patients with metastatic non-small cell lung cancer (NSCLC), the number of patients who experience a sustained response to treatment remains limited. The majority of patients will eventually develop progressive disease. Microbiome-based biomarkers offer an opportunity to identify patients who may have a poor response to ICI-based regimens using non-invasive methods, and potentially, the microbiota may be amenable to therapy-enhancing alteration. However, a deep understanding of the longitudinal dynamics of gut microbial features in patients treated with ICIs in NSCLC, a feature of likely importance for microbiome-based therapeutics, remains limited. In this study, we show that patients with NSCLC who experience a poor response to an ICI-based regimen show a loss of intra-individual microbiome stability in the first 4 months during treatment with an ICI-based regimen, independent of antibiotic exposure. Longitudinal loss of microbiome stability was also associated with poor response in patients with melanoma. To identify key microbial species associated with progression, recursive feature elimination with random forest classifiers was used to identify temporally-associated microbial species associated with disease progression. An index of these progression-associated species was able to predict clinical outcomes based on pre-treatment fecal samples, with validation on an independent lung cancer cohort. Together, our data show that microbial instability may be an early indicator of ICI-resistance in patients with NSCLC and melanoma, with the potential to be developed into biomarkers of primary resistance to ICI-based regimens. Citation Format: Yujie Zhao, Jarushka Naidoo, Michael Conroy, Jacqueline T. Ferri, Joell J. Gills, Krista Y. Chen, James R. White, Sara Glass, Willaim O. Assan, Kimberly Peloza, Megan D. Schollenberger, William H. Sharfman, Kristen Marrone, Patrick M. Forde, Julie R. Brahmer, Valsamo (Elsa) Anagnostou, Drew M. Pardoll, Joseph Murray, Evan J. Lipson, Cynthia L. Sears, Fyza Y. Shaikh. Longitudinal loss of microbiome stability is associated with poor response to immune checkpoint inhibitors in lung cancer and melanoma [abstract]. In: Proceedings of the American Association for Cancer Research Annual Meeting 2026; Part 1 (Regular Abstracts); 2026 Apr 17-22; San Diego, CA. Philadelphia (PA): AACR; Cancer Res 2026;86(7 Suppl):Abstract nr 6469.

Authors

Institutions

Publication Details

Journal
Cancer Research
Published
2026-04-03
DOI
https://doi.org/10.1158/1538-7445.am2026-6469
Primary Topic
Gut microbiota and health
Type
article
Field-Weighted Citation Impact
0.00
Controls
|||
ALL TIME
JAN
FEB
MAR
APR
MAY
JUN
JUL
AUG
SEP
OCT
article

Abstract 6469: Longitudinal loss of microbiome stability is associated with poor response to immune checkpoint inhibitors in lung cancer and melanoma

Kimberly E. Peloza, Sara K Glass, Evan J. Lipson, Joell J. Gills et al.
Cancer Research
Gut microbiota and health
article

Abstract 6469: Longitudinal loss of microbiome stability is associated with poor response to immune checkpoint inhibitors in lung cancer and melanoma

Kimberly E. Peloza, Sara K Glass, Evan J. Lipson, Joell J. Gills, Julie R. Brahmer, Jarushka Naidoo, D. Pardoll, Kristen Ashley Marrone, Joseph C. Murray, Megan D. Schollenberger, Fyza Y. Shaikh, Y. Zhao, J T Ferri, Willaim O. Assan, Michael Conroy, Patrick M. Forde, Cynthia L. Sears, James R. White, Valsamo (Elsa) K. Anagnostou, Krista Y. Chen, William H. Sharfman
article en

Abstract

Abstract While immune checkpoint inhibitors (ICI)-based regimens and chemo-immunotherapy combinations (chemo-ICI) are now first-line therapy for patients with metastatic non-small cell lung cancer (NSCLC), the number of patients who experience a sustained response to treatment remains limited. The majority of patients will eventually develop progressive disease. Microbiome-based biomarkers offer an opportunity to identify patients who may have a poor response to ICI-based regimens using non-invasive methods, and potentially, the microbiota may be amenable to therapy-enhancing alteration. However, a deep understanding of the longitudinal dynamics of gut microbial features in patients treated with ICIs in NSCLC, a feature of likely importance for microbiome-based therapeutics, remains limited. In this study, we show that patients with NSCLC who experience a poor response to an ICI-based regimen show a loss of intra-individual microbiome stability in the first 4 months during treatment with an ICI-based regimen, independent of antibiotic exposure. Longitudinal loss of microbiome stability was also associated with poor response in patients with melanoma. To identify key microbial species associated with progression, recursive feature elimination with random forest classifiers was used to identify temporally-associated microbial species associated with disease progression. An index of these progression-associated species was able to predict clinical outcomes based on pre-treatment fecal samples, with validation on an independent lung cancer cohort. Together, our data show that microbial instability may be an early indicator of ICI-resistance in patients with NSCLC and melanoma, with the potential to be developed into biomarkers of primary resistance to ICI-based regimens. Citation Format: Yujie Zhao, Jarushka Naidoo, Michael Conroy, Jacqueline T. Ferri, Joell J. Gills, Krista Y. Chen, James R. White, Sara Glass, Willaim O. Assan, Kimberly Peloza, Megan D. Schollenberger, William H. Sharfman, Kristen Marrone, Patrick M. Forde, Julie R. Brahmer, Valsamo (Elsa) Anagnostou, Drew M. Pardoll, Joseph Murray, Evan J. Lipson, Cynthia L. Sears, Fyza Y. Shaikh. Longitudinal loss of microbiome stability is associated with poor response to immune checkpoint inhibitors in lung cancer and melanoma [abstract]. In: Proceedings of the American Association for Cancer Research Annual Meeting 2026; Part 1 (Regular Abstracts); 2026 Apr 17-22; San Diego, CA. Philadelphia (PA): AACR; Cancer Res 2026;86(7 Suppl):Abstract nr 6469.

Cancer ResearchVol. 86(7_Supplement)
Bloomberg (United States) (US), Johns Hopkins University (US), Johns Hopkins Hospital (US), Resphera Biosciences (US), Sidney Kimmel Comprehensive Cancer Center (US), University of Baltimore (US)
No poverty
Openalex Percentile: Top 30%
Gut microbiota and health
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.