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Intestinal Akkermansia muciniphila predicts clinical response to PD-1 blockade in patients with advanced non-small-cell lung cancer.
Derosa, Lisa; Routy, Bertrand; Thomas, Andrew Maltez; Iebba, Valerio; Zalcman, Gerard; Friard, Sylvie; Mazieres, Julien; Audigier-Valette, Clarisse; Moro-Sibilot, Denis; Goldwasser, François; Silva, Carolina Alves Costa; Terrisse, Safae; Bonvalet, Melodie; Scherpereel, Arnaud; Pegliasco, Hervé; Richard, Corentin; Ghiringhelli, François; Elkrief, Arielle; Desilets, Antoine; Blanc-Durand, Felix; Cumbo, Fabio; Blanco, Aitor; Boidot, Romain; Chevrier, Sandy; Daillère, Romain; Kroemer, Guido; Alla, Laurie; Pons, Nicolas; Le Chatelier, Emmanuelle; Galleron, Nathalie; Roume, Hugo; Dubuisson, Agathe; Bouchard, Nicole; Messaoudene, Meriem; Drubay, Damien; Deutsch, Eric; Barlesi, Fabrice; Planchard, David; Segata, Nicola; Martinez, Stéphanie; Zitvogel, Laurence; Soria, Jean-Charles; Besse, Benjamin.
Afiliação
  • Derosa L; Gustave Roussy Cancer Campus, Villejuif, France.
  • Routy B; Cancer Medicine Department, Gustave Roussy, Villejuif, France.
  • Thomas AM; Institut National de la Santé Et de la Recherche Médicale (INSERM) U1015, Equipe Labellisée, Ligue Nationale contre le Cancer, Villejuif, France.
  • Iebba V; Université Paris-Saclay, Ile-de-France, France.
  • Zalcman G; Department of Medicine, Centre Hospitalier de l'Université de Montréal (CHUM), Hematology-Oncology Division, Montréal, Quebec, Canada.
  • Friard S; Centre de Recherche du CHUM (CRCHUM), Montréal, Quebec, Canada.
  • Mazieres J; Department CIBIO, University of Trento, Trento, Italy.
  • Audigier-Valette C; European Institute of Oncology (IEO) IRCCS, Milan, Italy.
  • Moro-Sibilot D; Department of Medical, Surgical and Health Sciences, University of Trieste, Trieste, Italy.
  • Goldwasser F; Thoracic Oncology Department-CIC1425/CLIP2 Paris-Nord, Hospital Bichat-Claude Bernard, AP-HP, Université Paris-Diderot, Paris, France.
  • Silva CAC; Pneumology Department, Foch Hospital, Suresnes, France.
  • Terrisse S; Department of Pneumology, Toulouse University Hospital, Toulouse, France.
  • Bonvalet M; Pneumology Department, Centre Hospitalier Toulon Sainte-Musse, Toulon, France.
  • Scherpereel A; Department of Thoracic Oncology, Centre Hospitalier Universitaire, Grenoble, France.
  • Pegliasco H; UPR 4466, Paris Descartes University, Sorbonne Paris Cité, Paris, France.
  • Richard C; Department of Medical Oncology, Cochin Hospital, Assistance Publique-Hôpitaux de Paris, Paris, France.
  • Ghiringhelli F; Immunomodulatory Therapies Multidisciplinary Study Group (CERTIM), Paris, France.
  • Elkrief A; Gustave Roussy Cancer Campus, Villejuif, France.
  • Desilets A; Cancer Medicine Department, Gustave Roussy, Villejuif, France.
  • Blanc-Durand F; Gustave Roussy Cancer Campus, Villejuif, France.
  • Cumbo F; Gustave Roussy Cancer Campus, Villejuif, France.
  • Blanco A; Department of Pulmonary and Thoracic Oncology, University of Lille, University Hospital (CHU), Lille, France.
  • Boidot R; Pulmonary Department, European Hospital, Marseille, France.
  • Chevrier S; Department of Medicine, Centre Hospitalier de l'Université de Montréal (CHUM), Hematology-Oncology Division, Montréal, Quebec, Canada.
  • Daillère R; Centre de Recherche du CHUM (CRCHUM), Montréal, Quebec, Canada.
  • Kroemer G; Cancer Biology Transfer Platform, Centre Georges-François Leclerc, Dijon, France.
  • Alla L; Centre de Recherche INSERM LNC-UMR1231, Dijon, France.
  • Pons N; Department of Medical Oncology, Centre Georges-François Leclerc, Dijon, France.
  • Le Chatelier E; Department of Medicine, Centre Hospitalier de l'Université de Montréal (CHUM), Hematology-Oncology Division, Montréal, Quebec, Canada.
  • Galleron N; Centre de Recherche du CHUM (CRCHUM), Montréal, Quebec, Canada.
  • Roume H; Department of Medicine, Centre Hospitalier de l'Université de Montréal (CHUM), Hematology-Oncology Division, Montréal, Quebec, Canada.
  • Dubuisson A; Centre de Recherche du CHUM (CRCHUM), Montréal, Quebec, Canada.
  • Bouchard N; Gustave Roussy Cancer Campus, Villejuif, France.
  • Messaoudene M; Department CIBIO, University of Trento, Trento, Italy.
  • Drubay D; Department CIBIO, University of Trento, Trento, Italy.
  • Deutsch E; Unit of Molecular Biology, Department of Biology and Pathology of Tumors, Georges-François Leclerc Cancer Center, UNICANCER, Dijon, France.
  • Barlesi F; Unit of Molecular Biology, Department of Biology and Pathology of Tumors, Georges-François Leclerc Cancer Center, UNICANCER, Dijon, France.
  • Planchard D; EverImmune, Gustave Roussy Cancer Campus, Villejuif, France.
  • Segata N; Gustave Roussy Cancer Campus, Villejuif, France.
  • Martinez S; UPR 4466, Paris Descartes University, Sorbonne Paris Cité, Paris, France.
  • Zitvogel L; Centre de Recherche des Cordeliers, INSERM U1138, Equipe labellisée-Ligue contre le cancer, Université de Paris, Institut Universitaire de France, Paris, France.
  • Soria JC; Metabolomics and Cell Biology Platforms, Institut Gustave Roussy, Villejuif, France.
  • Besse B; Pôle de Biologie, Hôpital Européen Georges Pompidou, AP-HP, Paris, France.
Nat Med ; 28(2): 315-324, 2022 02.
Article em En | MEDLINE | ID: mdl-35115705
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.
Assuntos

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Carcinoma Pulmonar de Células não Pequenas / Neoplasias Pulmonares Idioma: En Ano de publicação: 2022 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Carcinoma Pulmonar de Células não Pequenas / Neoplasias Pulmonares Idioma: En Ano de publicação: 2022 Tipo de documento: Article