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Immune Profiling of Combined Hepatocellular- Cholangiocarcinoma Reveals Distinct Subtypes and Activation of Gene Signatures Predictive of Response to Immunotherapy.
Nguyen, Cong Trung; Caruso, Stefano; Maille, Pascale; Beaufrère, Aurélie; Augustin, Jérémy; Favre, Loetitia; Pujals, Anaïs; Boulagnon-Rombi, Camille; Rhaiem, Rami; Amaddeo, Giuliana; di Tommaso, Luca; Luciani, Alain; Regnault, Hélène; Brustia, Raffaele; Scatton, Olivier; Charlotte, Frédéric; Brochériou, Isabelle; Sommacale, Daniele; Soussan, Patrick; Leroy, Vincent; Laurent, Alexis; Le, Van Ky; Ta, Van To; Trinh, Hong Son; Tran, Thi Lan; Gentien, David; Rapinat, Audrey; Nault, Jean Charles; Allaire, Manon; Mulé, Sebastien; Zucman-Rossi, Jessica; Pawlotsky, Jean-Michel; Tournigand, Christophe; Lafdil, Fouad; Paradis, Valérie; Calderaro, Julien.
Afiliação
  • Nguyen CT; Université Paris Est Créteil, INSERM, IMRB, Créteil, France.
  • Caruso S; INSERM, U955, Equipe 18 "Physiopathologie et Thérapeutiques des Hépatites Virales Chroniques et des cancers liés", Créteil, France.
  • Maille P; INSERM UMR-1162, Génomique Fonctionnelle des Tumeurs Solides, Paris, France.
  • Beaufrère A; Université Paris Est Créteil, INSERM, IMRB, Créteil, France.
  • Augustin J; Assistance Publique-Hôpitaux de Paris, Hôpital Henri Mondor, Département de Pathologie, Créteil, France.
  • Favre L; Assistance Publique-Hôpitaux de Paris, Hôpital Beaujon, Service d'Anatomo-Pathologie, Clichy, France.
  • Pujals A; Assistance Publique-Hôpitaux de Paris, Hôpital de la Pitié-Salpêtrière, Service d'Anatomie et de Cytologie Pathologiques, Sorbonne Université, Paris, France.
  • Boulagnon-Rombi C; Université Paris Est Créteil, INSERM, IMRB, Créteil, France.
  • Rhaiem R; Assistance Publique-Hôpitaux de Paris, Hôpital Henri Mondor, Département de Pathologie, Créteil, France.
  • Amaddeo G; Université Paris Est Créteil, INSERM, IMRB, Créteil, France.
  • di Tommaso L; Assistance Publique-Hôpitaux de Paris, Hôpital Henri Mondor, Département de Pathologie, Créteil, France.
  • Luciani A; Centre Hospitalier Universitaire de Reims, Service d'Anatomie et de Cytologie Pathologiques, Reims, France.
  • Regnault H; Hôpital Robert Debré, Service de Chirurgie Digestive et Hépatobiliaire, Reims, France.
  • Brustia R; Université Paris Est Créteil, INSERM, IMRB, Créteil, France.
  • Scatton O; INSERM, U955, Equipe 18 "Physiopathologie et Thérapeutiques des Hépatites Virales Chroniques et des cancers liés", Créteil, France.
  • Charlotte F; Assistance Publique-Hôpitaux de Paris, Hôpital Henri Mondor, Service d'Hépatologie, Créteil, France.
  • Brochériou I; Department of Pathology, Humanitas University, Humanitas Clinical and Research Center, IRCCS, Rozzano, Milan, Italy.
  • Sommacale D; Université Paris Est Créteil, INSERM, IMRB, Créteil, France.
  • Soussan P; INSERM, U955, Equipe 18 "Physiopathologie et Thérapeutiques des Hépatites Virales Chroniques et des cancers liés", Créteil, France.
  • Leroy V; Assistance Publique-Hôpitaux de Paris, Hôpital Henri Mondor, Service d'Imagerie Médicale, Créteil, France.
  • Laurent A; Assistance Publique-Hôpitaux de Paris, Hôpital Henri Mondor, Service d'Hépatologie, Créteil, France.
  • Le VK; Assistance Publique-Hôpitaux de Paris, Hôpital de la Pitié-Salpêtrière, Service de Chirurgie Digestive, Hépato-Bilio-Pancréatique et Transplantation Hépatique, Paris, France.
  • Ta VT; Assistance Publique-Hôpitaux de Paris, Hôpital de la Pitié-Salpêtrière, Service de Chirurgie Digestive, Hépato-Bilio-Pancréatique et Transplantation Hépatique, Paris, France.
  • Trinh HS; Assistance Publique-Hôpitaux de Paris, Hôpital de la Pitié-Salpêtrière, Service d'Anatomie et de Cytologie Pathologiques, Sorbonne Université, Paris, France.
  • Tran TL; Assistance Publique-Hôpitaux de Paris, Hôpital de la Pitié-Salpêtrière, Service d'Anatomie et de Cytologie Pathologiques, Sorbonne Université, Paris, France.
  • Gentien D; Université Paris Est Créteil, INSERM, IMRB, Créteil, France.
  • Rapinat A; INSERM, U955, Equipe 18 "Physiopathologie et Thérapeutiques des Hépatites Virales Chroniques et des cancers liés", Créteil, France.
  • Nault JC; Assistance Publique-Hôpitaux de Paris, Hôpital Henri Mondor, Service de Chirurgie Digestive et Hépato-bilio-pancréatique, Créteil, France.
  • Allaire M; Centre National de la Recherche Scientifique (CNRS, ERL8255), Institut National de la Santé et de la Recherche Médicale (Inserm, UMR1135), Sorbonne Universités, Paris, France.
  • Mulé S; Université Paris Est Créteil, INSERM, IMRB, Créteil, France.
  • Zucman-Rossi J; INSERM, U955, Equipe 18 "Physiopathologie et Thérapeutiques des Hépatites Virales Chroniques et des cancers liés", Créteil, France.
  • Pawlotsky JM; Assistance Publique-Hôpitaux de Paris, Hôpital Henri Mondor, Service d'Hépatologie, Créteil, France.
  • Tournigand C; Université Paris Est Créteil, INSERM, IMRB, Créteil, France.
  • Lafdil F; Assistance Publique-Hôpitaux de Paris, Hôpital Henri Mondor, Service de Chirurgie Digestive et Hépato-bilio-pancréatique, Créteil, France.
  • Paradis V; Department of Pathology, National Cancer Hospital, Hanoi, Vietnam.
  • Calderaro J; Department of Pathology, National Cancer Hospital, Hanoi, Vietnam.
Clin Cancer Res ; 28(3): 540-551, 2022 02 01.
Article em En | MEDLINE | ID: mdl-34785581
PURPOSE: Combined hepatocellular-cholangiocarcinoma (cHCC-CCA) is a rare malignancy associated with an overall poor prognosis. We aimed to investigate the immune profile of cHCC-CCA and determine its impact on disease outcome. EXPERIMENTAL DESIGN: We performed a multicenter study of 96 patients with cHCC-CCA. Gene expression profile was analyzed using nCounter PanCancer IO 360 Panel. Densities of main immune cells subsets were quantified from digital slides of IHC stainings. Genetic alterations were investigated using targeted next-generation sequencing. RESULTS: Two main immune subtypes of cHCC-CCA were identified by clustering analysis: an "immune-high" (IH) subtype (57% of the cases) and an "immune-low" (IL) subtype (43% of the cases). Tumors classified as IH showed overexpression of genes related to immune cells recruitment, adaptive and innate immunity, antigen presentation, cytotoxicity, immune suppression, and inflammation (P < 0.0001). IH cHCC-CCAs also displayed activation of gene signatures recently shown to be associated with response to immunotherapy in patients with HCC. Quantification of immunostainings confirmed that IH tumors were also characterized by higher densities of immune cells. Immune subtypes were not associated with any genetic alterations. Finally, multivariate analysis showed that the IH subtype was an independent predictor of improved overall survival. CONCLUSIONS: We have identified a subgroup of cHCC-CCA that displays features of an ongoing intratumor immune response, along with an activation of gene signatures predictive of response to immunotherapy in HCC. This tumor subclass is associated with an improved clinical outcome. These findings suggest that a subset of patients with cHCC-CCA may benefit from immunomodulating therapeutic approaches.
Assuntos

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Neoplasias dos Ductos Biliares / Colangiocarcinoma / Carcinoma Hepatocelular / Imunoterapia / Neoplasias Hepáticas / Neoplasias Primárias Múltiplas Tipo de estudo: Clinical_trials / Diagnostic_studies / Prognostic_studies / Risk_factors_studies Limite: Adult / Aged / Aged80 / Female / Humans / Male / Middle aged Idioma: En Revista: Clin Cancer Res Assunto da revista: NEOPLASIAS Ano de publicação: 2022 Tipo de documento: Article País de afiliação: França

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Neoplasias dos Ductos Biliares / Colangiocarcinoma / Carcinoma Hepatocelular / Imunoterapia / Neoplasias Hepáticas / Neoplasias Primárias Múltiplas Tipo de estudo: Clinical_trials / Diagnostic_studies / Prognostic_studies / Risk_factors_studies Limite: Adult / Aged / Aged80 / Female / Humans / Male / Middle aged Idioma: En Revista: Clin Cancer Res Assunto da revista: NEOPLASIAS Ano de publicação: 2022 Tipo de documento: Article País de afiliação: França