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Unresectable hepatocellular carcinoma at dawn of immunotherapy era: real-world data from the French prospective CHIEF cohort.
Nguyen-Khac, Eric; Nahon, Pierre; Ganry, Olivier; Ben Khadhra, Hajer; Merle, Philippe; Amaddeo, Giuliana; Ganne-Carrie, Nathalie; Silvain, Christine; Peron, Jean-Marie; Mathurin, Philippe; Anty, Rodolphe; Uguen, Thomas; Decaens, Thomas; Riachi, Ghassan; Bouattour, Mohamed; Baron, Aurore; Bronowicki, Jean-Pierre; Pageaux, Georges-Philippe; Rosmorduc, Olivier; Ducournau, Gérard; Gilberg, Mélina; Tanang, Alexandre; Dupin, Julien; Gilbert-Marceau, Anika; Blanc, Jean-Frédéric.
Afiliación
  • Nguyen-Khac E; Hepato-Gastroenterology Department, CHU Amiens, Amiens.
  • Nahon P; CHU Bobigny, APHP, Liver Unit, Bobigny; Université Sorbonne Paris Nord, F-93000 Bobigny; Inserm, UMR-1138, Université de Paris, Paris.
  • Ganry O; Hepato-Gastroenterology Department, CHU Amiens, Amiens.
  • Ben Khadhra H; Hepato-Gastroenterology Department, CHU Amiens, Amiens.
  • Merle P; Hepatology Unit, Groupement Hospitalier Lyon Nord, Hospices Civils de Lyon.
  • Amaddeo G; Hepatology Department, Hôpital Henri Mondor, APHP, Paris.
  • Ganne-Carrie N; CHU Bobigny, APHP, Liver Unit, Bobigny; Université Sorbonne Paris Nord, F-93000 Bobigny; Inserm, UMR-1138, Université de Paris, Paris.
  • Silvain C; Hepato-Gastroenterology Department, CHU Poitiers, Poitiers.
  • Peron JM; Hepato-Gastroenterology Department, CHU Toulouse, Toulouse.
  • Mathurin P; Hepato-Gastroenterology Department, CHU Lille, Lille.
  • Anty R; Hepato-Gastroenterology Department, Université Côte d'Azur, CHU, INSERM, U1065, C3M, Nice.
  • Uguen T; Hepato-Gastroenterology Department, CHU Rennes, Rennes.
  • Decaens T; Hepato-Gastroenterology Department, Université Grenoble Alpes, Service d'Hépato-Gastroentérologie, Centre Hospitalier universitaire Grenoble-Alpes, Institute for Advanced Biosciences, Research Center UGA/Inserm U 1209/CNRS 5309, Grenoble.
  • Riachi G; Hepato-Gastroenterology Department, CHU Rouen, Rouen.
  • Bouattour M; Hepatology Department, Hôpital Beaujon, APHP, Paris.
  • Baron A; Hepato-Gastroenterology Department, CH sud-francilien, Corbeil-Essonnes.
  • Bronowicki JP; Hepato-Gastroenterology Department, CHU Nancy, Nancy.
  • Pageaux GP; Hepato-Gastroenterology Department, CHU Montpellier, Montpellier.
  • Rosmorduc O; Hepatology Department, Hôpital Paul Brousse, APHP, Paris.
  • Ducournau G; Hepato-Gastroenterology Department, CHU Amiens, Amiens.
  • Gilberg M; Hepato-Gastroenterology Department, ROCHE SAS.
  • Tanang A; Hepato-Gastroenterology Department, ROCHE SAS.
  • Dupin J; Hepato-Gastroenterology Department, ROCHE SAS.
  • Gilbert-Marceau A; Hepato-Gastroenterology Department, ROCHE SAS.
  • Blanc JF; Hepato-Gastroenterology Department, CHU Bordeaux, Bordeaux, France.
Eur J Gastroenterol Hepatol ; 35(10): 1168-1177, 2023 10 01.
Article en En | MEDLINE | ID: mdl-37577805
ABSTRACT
BACKGROUND AND

OBJECTIVES:

Hepatocellular carcinoma epidemiological data are limited in France. The Epidemio Liver Immunotherapy Tecentriq outcome research (ELITor) retrospective study, based on real-world data from the Carcinome HépatocellulaIrE en France (CHIEF) French cohort of hepatocellular carcinoma patients, aimed to get insight into the treatment patterns, the sociodemographic, clinical, biological, and etiological characteristics, and the quality of life of patients with unresectable hepatocellular carcinoma. METHODS AND

RESULTS:

Between 1 September 2019 and 4 December 2020, 367 patients from the CHIEF cohort received at least one locoregional (52.8%) chemoembolization or radioembolization or systemic treatment (88.3%) and were selected for ELITor. Most patients had a Barcelona Clinic Liver Cancer (BCLC) C (93.2%) hepatocellular carcinoma stage and were affected by cirrhosis (67.7%). Alcohol was confirmed as the main etiology both as a single etiology (29.1%) and in association with other risk factors (26.9%), mainly metabolic disorders (16.2%).Tyrosine-kinase inhibitors, mainly sorafenib, were the most administered systemic treatments in first line. Patients who received at least one combination of atezolizumab and bevacizumab during the study period ( N  = 53) had a better performance status and less portal hypertension frequency than the overall population and more hepatitis B virus infection and fewer metabolic disorders as single etiology. Overall, the global health score before treatment (62.3 ±â€…21.9) was in line with that of reference cancer patients and worsened in 51.9% of the cases after first-line palliative-intent treatment.

CONCLUSION:

This study provided real-life data on advanced hepatocellular carcinoma characteristics and treatment patterns and described the first patients to receive the atezolizumab-bevacizumab combination before it became the new standard of care for advanced hepatocellular carcinoma.
Asunto(s)

Texto completo: 1 Bases de datos: MEDLINE Asunto principal: Quimioembolización Terapéutica / Carcinoma Hepatocelular / Neoplasias Hepáticas Tipo de estudio: Observational_studies / Risk_factors_studies Límite: Humans Idioma: En Revista: Eur J Gastroenterol Hepatol Asunto de la revista: GASTROENTEROLOGIA Año: 2023 Tipo del documento: Article

Texto completo: 1 Bases de datos: MEDLINE Asunto principal: Quimioembolización Terapéutica / Carcinoma Hepatocelular / Neoplasias Hepáticas Tipo de estudio: Observational_studies / Risk_factors_studies Límite: Humans Idioma: En Revista: Eur J Gastroenterol Hepatol Asunto de la revista: GASTROENTEROLOGIA Año: 2023 Tipo del documento: Article