| Literature DB >> 35115705 |
Lisa Derosa1,2,3,4, Bertrand Routy5,6, Andrew Maltez Thomas7,8, Valerio Iebba9, Gerard Zalcman10, Sylvie Friard11, Julien Mazieres12, Clarisse Audigier-Valette13, Denis Moro-Sibilot14, François Goldwasser15,16,17, Carolina Alves Costa Silva1,2, Safae Terrisse1, Melodie Bonvalet1, Arnaud Scherpereel18, Hervé Pegliasco19, Corentin Richard5,6, François Ghiringhelli20,21,22, Arielle Elkrief5,6, Antoine Desilets5,6, Felix Blanc-Durand1, Fabio Cumbo7, Aitor Blanco7, Romain Boidot23, Sandy Chevrier23, Romain Daillère24, Guido Kroemer1,15,25,26,27, Laurie Alla28, Nicolas Pons28, Emmanuelle Le Chatelier28, Nathalie Galleron28, Hugo Roume28, Agathe Dubuisson1, Nicole Bouchard29, Meriem Messaoudene5,6, Damien Drubay30, Eric Deutsch1,4,31,32, Fabrice Barlesi1,2, David Planchard1,2, Nicola Segata7,8, Stéphanie Martinez33, Laurence Zitvogel34,35,36,37, Jean-Charles Soria1, Benjamin Besse1,2,4.
Abstract
Aside from PD-L1 expression, biomarkers of response to immune checkpoint inhibitors (ICIs) in non-small-cell lung cancer (NSCLC) are needed. In a previous retrospective analysis, we documented that fecal Akkermansia muciniphila (Akk) was associated with clinical benefit of ICI in patients with NSCLC or kidney cancer. In the current study, we performed shotgun-metagenomics-based microbiome profiling in a large cohort of patients with advanced NSCLC (n = 338) treated with first- or second-line ICIs to prospectively validate the predictive value of fecal Akk. Baseline stool Akk was associated with increased objective response rates and overall survival in multivariate analyses, independent of PD-L1 expression, antibiotics, and performance status. Intestinal Akk was accompanied by a richer commensalism, including Eubacterium hallii and Bifidobacterium adolescentis, and a more inflamed tumor microenvironment in a subset of patients. However, antibiotic use (20% of cases) coincided with a relative dominance of Akk above 4.8% accompanied with the genus Clostridium, both associated with resistance to ICI. Our study shows significant differences in relative abundance of Akk that may represent potential biomarkers to refine patient stratification in future studies.Entities:
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Year: 2022 PMID: 35115705 PMCID: PMC9330544 DOI: 10.1038/s41591-021-01655-5
Source DB: PubMed Journal: Nat Med ISSN: 1078-8956 Impact factor: 87.241