Efficacy and safety of infliximab in patients with autoimmune hepatitis.


Journal

Hepatology (Baltimore, Md.)
ISSN: 1527-3350
Titre abrégé: Hepatology
Pays: United States
ID NLM: 8302946

Informations de publication

Date de publication:
06 Sep 2024
Historique:
received: 08 05 2024
accepted: 24 08 2024
medline: 9 9 2024
pubmed: 9 9 2024
entrez: 9 9 2024
Statut: aheadofprint

Résumé

A limited number of drugs are used as standard or alternative therapies in autoimmune hepatitis (AIH). No specific-recommendations are available for patients failing to respond to these therapies. We analyzed the efficacy and safety of infliximab in patients with AIH. We performed a retrospective study of 42 patients with AIH who received infliximab at 21 liver centers in 12 countries. Patients were categorized according to the reason for infliximab therapy. Patients in group 1 (n=20) had failed standard, second-line (mycophenolate mofetil and 6-mercaptopurine) or third-line (tacrolimus or cyclosporine) therapy. In group 2 (n=22), infliximab was given for treatment of concomitant extrahepatic autoimmune diseases. Patients received a median of 17 (range: 3-104) infliximab infusions. Complete biochemical response (CR) was achieved or maintained in 33 (78%) patients during infliximab therapy. In group 1, infliximab induced CR in 11 of 20 (55%) patients. In group 2, 16 patients with CR prior to infliximab maintained remission, and the remaining six patients with active AIH (five on standard and one on both second and third-line therapy) showed CR following infliximab therapy. Infliximab led to CR in 75% (6/8) of non-responders to second-line and in 46% (6/13) of failing third-line therapy. Overall, 65% (17/26) of the patients with active AIH achieved CR on infliximab. Infliximab was discontinued in three patients of group 1. One patient had a severe allergic reaction and two developed anti-infliximab autoantibodies. Our study suggests that infliximab may be an effective and safe rescue therapy in AIH.

Sections du résumé

BACKGROUND AND AIMS OBJECTIVE
A limited number of drugs are used as standard or alternative therapies in autoimmune hepatitis (AIH). No specific-recommendations are available for patients failing to respond to these therapies. We analyzed the efficacy and safety of infliximab in patients with AIH.
APPROACH AND RESULTS RESULTS
We performed a retrospective study of 42 patients with AIH who received infliximab at 21 liver centers in 12 countries. Patients were categorized according to the reason for infliximab therapy. Patients in group 1 (n=20) had failed standard, second-line (mycophenolate mofetil and 6-mercaptopurine) or third-line (tacrolimus or cyclosporine) therapy. In group 2 (n=22), infliximab was given for treatment of concomitant extrahepatic autoimmune diseases. Patients received a median of 17 (range: 3-104) infliximab infusions. Complete biochemical response (CR) was achieved or maintained in 33 (78%) patients during infliximab therapy. In group 1, infliximab induced CR in 11 of 20 (55%) patients. In group 2, 16 patients with CR prior to infliximab maintained remission, and the remaining six patients with active AIH (five on standard and one on both second and third-line therapy) showed CR following infliximab therapy. Infliximab led to CR in 75% (6/8) of non-responders to second-line and in 46% (6/13) of failing third-line therapy. Overall, 65% (17/26) of the patients with active AIH achieved CR on infliximab. Infliximab was discontinued in three patients of group 1. One patient had a severe allergic reaction and two developed anti-infliximab autoantibodies.
CONCLUSION CONCLUSIONS
Our study suggests that infliximab may be an effective and safe rescue therapy in AIH.

Identifiants

pubmed: 39250458
doi: 10.1097/HEP.0000000000001089
pii: 01515467-990000000-01020
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Informations de copyright

Copyright © 2024 American Association for the Study of Liver Diseases.

Auteurs

Cumali Efe (C)

Department of Gastroenterology, Harran University Hospital, Şanlıurfa, Turkey.

Ellina Lytvyak (E)

University of Alberta, Division of Gastroenterology and Liver Unit, Edmonton, Alberta, Canada.

Tuğçe Eşkazan (T)

Department of Gastroenterology, Cerrahpaşa School of Medicine, İstanbul, Turkey.

Rodrigo Liberal (R)

Gastroenterology and Hepatology Department, Centro Hospitalar e Universitário de São João, Porto, Portugal; World Gastroenterology Organization (WGO) Porto Training Center, Portugal.

Theodoros Androutsakos (T)

Department of Pathophysiology, National and Kapodistrian University of Athens, Medical School, Athens, Greece.

Dilara Turan Gökçe (D)

Department of Gastroenterology, Sincan state Hospital, Ankara, Turkey.

Benedetta Terziroli Beretta-Piccoli (B)

Faculty of Biomedical Sciences, Università Della Svizzera Italiana, 6900, Lugano, Switzerland. Epatocentro Ticino, Via Soldino 9, 6900, Lugano. Collaborative partner European Reference Network on Hepatological Diseases (ERN RARE-LIVER), Hamburg, Germany.

Maciej Janik (M)

Department of Hepatology, Transplantology and Internal Medicine, Medical University of Warsaw, Warsaw, Poland. Full member European Reference Network on Hepatological Diseases (ERN RARE-LIVER), Hamburg, Germany.

Christine Bernsmeier (C)

Department of Biomedicine, University of Basel, Switzerland; University Centre for Gastrointestinal and Liver Diseases, Basel, Switzerland.

Pinelopi Arvaniti (P)

Department of Medicine and Research Laboratory of Internal Medicine, Expertise Center of Greece in Autoimmune Liver Diseases, General University Hospital of Larissa. Full member European Reference Network on Hepatological Diseases (ERN RARE-LIVER), Hamburg, Germany.

Piotr Milkiewicz (P)

Department of Hepatology, Transplantology and Internal Medicine, Medical University of Warsaw, Warsaw, Poland. Full member European Reference Network on Hepatological Diseases (ERN RARE-LIVER), Hamburg, Germany.
Translational Medicine Group, Pomeranian Medical University in Szczecin, Poland.

Ersin Batıbay (E)

Department of Gastroenterology, Harran University Hospital, Şanlıurfa, Turkey.

Osman Yüksekyayla (O)

Department of Gastroenterology, Harran University Hospital, Şanlıurfa, Turkey.

Ilkay Ergenç (I)

Institute of Liver Studies, King's College Hospital NHS Foundation Trust, London, UK; Collaborative partner European Reference Network on Hepatological Diseases (ERN RARE-LIVER).

Çiğdem Arıkan (Ç)

Department of Pediatric Gastroenterology and Hepatology, Koc University School of Medicine, Istanbul, Turkey.

Albert Friedrich Stättermayer (AF)

Division of Gastroenterology and Hepatology, Department of Internal Medicine III, Medical University of Vienna, Vienna, Austria. Rare Liver Disease (RALID), Affiliated partner European Reference Network for Rare Hepatological Diseases (ERN RARE-LIVER).

Sezgin Barutçu (S)

Gastroenterology, University of Gaziantep Medical Faculty, Department, Gaziantep, Turkey.

Mustafa Cengiz (M)

Department of Gastroenterology Gülhane Training and Research Hospital Ankara, Turkey.

Özlem Gül (Ö)

Department of Gastroenterology, Lokman Hekim Üniversitesi Ankara Hastanesi, Ankara, Turkey.

Alexandra Heurgue (A)

Department of Hepato-Gastroenterology, CHU Reims, Reims, France.

Michael A Heneghan (MA)

Institute of Liver Studies, King's College Hospital NHS Foundation Trust, London, UK; Collaborative partner European Reference Network on Hepatological Diseases (ERN RARE-LIVER).

Sumita Verma (S)

Brighton and Sussex Medical School and University Hospitals Sussex NHS Foundation Trust, Brighton, UK.

Tuğrul Purnak (T)

Division of Gastroenterology, Hepatology and Nutrition, McGovern Medical School, 6431 Fannin, MSB1.150, Houston, TX, 77030, USA.

Murat Törüner (M)

Department of Gastroenterology, Ankara University Medical Faculty, Ankara, Turkey.

Meral Akdogan Kayhan (M)

Department of Gastroenterology, Ankara City Hospital, Ankara, Turkiye.

Ibrahim Hatemi (I)

Department of Gastroenterology, Cerrahpaşa School of Medicine, İstanbul, Turkey.

Kalliopi Zachou (K)

Department of Medicine and Research Laboratory of Internal Medicine, Expertise Center of Greece in Autoimmune Liver Diseases, General University Hospital of Larissa. Full member European Reference Network on Hepatological Diseases (ERN RARE-LIVER), Hamburg, Germany.

Guilherme Macedo (G)

Gastroenterology and Hepatology Department, Centro Hospitalar e Universitário de São João, Porto, Portugal; World Gastroenterology Organization (WGO) Porto Training Center, Portugal.

Joost P H Drenth (JPH)

Department of Gastroenterology and Hepatology, Amsterdam University Medical Center, The Netherlands; Collaborative partner European Reference Network RARE-LIVER, Hamburg, Germany.

Einar Björnsson (E)

Faculty of Medicine, University of Iceland, Reykjavik; Department of Gastroenterology and Hepatology, Landspitali University Hospital, Reykjavik, Iceland.

Aldo J Montano-Loza (AJ)

University of Alberta, Division of Gastroenterology and Liver Unit, Edmonton, Alberta, Canada.

Staffan Wahlin (S)

Hepatology Division, Department of Upper GI Diseases, Karolinska Institutet and Karolinska University Hospital, Stockholm, Sweden. Full member European Reference Network on Hepatological Diseases (ERN RARE-LIVER), Hamburg, Germany.

Fatima Higuera-de la Tijera (F)

Gastroenterology and Hepatology Unit. Hospital General de México, Ciudad de México, México.

Classifications MeSH