Intestinal Akkermansia muciniphila predicts clinical response to PD-1 blockade in patients with advanced non-small-cell lung cancer

© 2022. The Author(s), under exclusive licence to Springer Nature America, Inc..

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.

Errataetall:

CommentIn: Cell Rep Med. 2022 May 17;3(5):100642. - PMID 35584634

Medienart:

E-Artikel

Erscheinungsjahr:

2022

Erschienen:

2022

Enthalten in:

Zur Gesamtaufnahme - volume:28

Enthalten in:

Nature medicine - 28(2022), 2 vom: 03. Feb., Seite 315-324

Sprache:

Englisch

Beteiligte Personen:

Derosa, Lisa [VerfasserIn]
Routy, Bertrand [VerfasserIn]
Thomas, Andrew Maltez [VerfasserIn]
Iebba, Valerio [VerfasserIn]
Zalcman, Gerard [VerfasserIn]
Friard, Sylvie [VerfasserIn]
Mazieres, Julien [VerfasserIn]
Audigier-Valette, Clarisse [VerfasserIn]
Moro-Sibilot, Denis [VerfasserIn]
Goldwasser, François [VerfasserIn]
Silva, Carolina Alves Costa [VerfasserIn]
Terrisse, Safae [VerfasserIn]
Bonvalet, Melodie [VerfasserIn]
Scherpereel, Arnaud [VerfasserIn]
Pegliasco, Hervé [VerfasserIn]
Richard, Corentin [VerfasserIn]
Ghiringhelli, François [VerfasserIn]
Elkrief, Arielle [VerfasserIn]
Desilets, Antoine [VerfasserIn]
Blanc-Durand, Felix [VerfasserIn]
Cumbo, Fabio [VerfasserIn]
Blanco, Aitor [VerfasserIn]
Boidot, Romain [VerfasserIn]
Chevrier, Sandy [VerfasserIn]
Daillère, Romain [VerfasserIn]
Kroemer, Guido [VerfasserIn]
Alla, Laurie [VerfasserIn]
Pons, Nicolas [VerfasserIn]
Le Chatelier, Emmanuelle [VerfasserIn]
Galleron, Nathalie [VerfasserIn]
Roume, Hugo [VerfasserIn]
Dubuisson, Agathe [VerfasserIn]
Bouchard, Nicole [VerfasserIn]
Messaoudene, Meriem [VerfasserIn]
Drubay, Damien [VerfasserIn]
Deutsch, Eric [VerfasserIn]
Barlesi, Fabrice [VerfasserIn]
Planchard, David [VerfasserIn]
Segata, Nicola [VerfasserIn]
Martinez, Stéphanie [VerfasserIn]
Zitvogel, Laurence [VerfasserIn]
Soria, Jean-Charles [VerfasserIn]
Besse, Benjamin [VerfasserIn]

Links:

Volltext

Themen:

B7-H1 Antigen
Journal Article
Programmed Cell Death 1 Receptor
Research Support, N.I.H., Extramural
Research Support, Non-U.S. Gov't

Anmerkungen:

Date Completed 26.04.2022

Date Revised 26.10.2022

published: Print-Electronic

CommentIn: Cell Rep Med. 2022 May 17;3(5):100642. - PMID 35584634

Citation Status MEDLINE

doi:

10.1038/s41591-021-01655-5

funding:

Förderinstitution / Projekttitel:

PPN (Katalog-ID):

NLM336483643