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Comparative effectiveness of tofacitinib versus upadacitinib for the treatment of acute severe ulcerative colitis

. 2025 Jul 26 ; () : . [epub] 20250726

Status Publisher Language English Country United States Media print-electronic

Document type Journal Article

Links

PubMed 40721074
DOI 10.1016/j.cgh.2025.07.025
PII: S1542-3565(25)00639-1
Knihovny.cz E-resources

BACKGROUND & AIMS: Tofacitinib and upadacitinib are Janus kinase (JAK) inhibitors that are increasingly used for the treatment of acute severe ulcerative colitis (ASUC). However, comparative analyses of safety and effectiveness have not been performed for their use in this setting. METHODS: This multicenter, retrospective study enrolled hospitalized adult patients treated with tofacitinib or upadacitinib for ASUC between January 2019 and June 2024. The main outcomes were clinical response, clinical remission, and colectomy-free survival. Propensity-adjusted analyses using inverse probability treatment weighting, and double robust estimations were used to control for confounding factors. RESULTS: In total, 111 patients (60 tofacitinib, 51 upadacitinib) were enrolled across 23 international centers. JAK inhibitors were used to induce response in 86 patients (77%) and used to maintain response after adequate intravenous steroid response in 25 (23%). The median follow up was 31 weeks (interquartile range, 13-64 weeks). Between days 3 and 7 after treatment initiation, upadacitinib was associated with greater response rates (84% vs 54%; P = .02), but response/remission was comparable at day 98 (45%/36% vs 55%/48%) and day 182 (29/29% vs 39/34%). Sub-analyses for JAK inhibitor use as salvage therapy (tofacitinib [n = 35] vs upadacitinib [n = 31]) showed similar effectiveness outcomes across both groups. The probabilities of colectomy-free survival at days 98 and 182 for tofacitinib and upadacitinib were 79% and 75% and 80% and 78%, respectively, with no significant differences in the comparison of survival curves (P = .99). Treatment failure rates (where JAK inhibitors were used to maintain remission) were similar at days 98 and 182. The frequency of adverse events was comparable. CONCLUSION: Tofacitinib and upadacitinib appear to have similar effectiveness and safety profiles when used for the treatment of ASUC.

Assistance Publique Hopitaux de Paris Lariboisiere Fernand Widal Hospital Paris France

Center for Advanced IBD Research and Treatment Kitasato University Kitasato Institute Hospital Tokyo Japan

CHU de Bordeaux Hôpital Haut Lévêque Service d'Hépato gastroentérologie et Oncologie Digestive Université de Bordeaux Bordeaux France

CHU Nantes Institut des Maladies de l'Appareil Digestif CIC Inserm 1413 Université de Nantes Nantes France

Clinical and Research Center for Inflammatory Bowel Diseases ISCARE Clinical Centre Prague Czech Republic

Colorectal Surgery Unit Pontificia Universidade Católica do Paraná Curitiba Brazil

Department of Gastroenterology and Clinical Nutrition CHU of Nice and University Côte d'Azur Nice France

Department of Gastroenterology and Endoscopy IRCCS San Raffaele Hospital Vita Salute San Raffaele University Milan Italy

Department of Gastroenterology CHRU Nancy INSERM NGERE Université de Lorraine Vandœuvre lès Nancy France

Department of Gastroenterology Faculty of Medicine and Health Örebro University Örebro Sweden

Department of Gastroenterology Hopital Henri Mondor APHP Créteil France

Department of Gastroenterology Lyon Sud Hospital Hospices Civils de Lyon and INSERM U1111 CIRI Lyon France

Department of Gastroenterology St George's University Hospitals NHS Foundation Trust London United Kingdom

Department of Gastroenterology St George's University Hospitals NHS Foundation Trust London United Kingdom; Hepato Gastroenterology and Digestive Oncology University Hospital CHU of Liège Liège Belgium

Department of Gastroenterology St George's University Hospitals NHS Foundation Trust London United Kingdom; Institute of Infection and Immunity City St George's University of London London United Kingdom

Department of Gastroenterology University Hospital of Marseille Nord University of Aix Marseille Marseille France

Department of Gastroenterology University Hospital of Saint Etienne Saint Etienne France

Department of Gastroenterology University of Ulsan College of Medicine Asan Medical Center Seoul Korea

Department of Gastroenterology Venizeleio General Hospital Heraklion Greece

Department of Hepatogastroenterology CHU St Eloi Montpellier Montpellier France

Division of Gastroenterology and Hepatology Department of Medicine University of Calgary Calgary Alberta Canada

Division of Gastroenterology Sheba Medical Center Ramat Gan Israel

Gastroenterology Unit Clermont Ferrand University Hospital Clermont Ferrand France

Hepato Gastro Enterology Department CHU Amiens Picardie and Peritox UMIR 1 O1 Université de Picardie Jules Verne Amiens France

School of Immunology and Microbial Sciences King's College London United Kingdom; Department of Gastroenterology St George's University Hospitals NHS Foundation Trust London United Kingdom

Université de Lorraine CHRU Inserm NGERE Nancy France

Université Lille Inserm CHU Lille U1286 INFINITE Institute for Translational Research in Inflammation Lille France

University of Chicago Medicine Inflammatory Bowel Disease Center Chicago Illinois

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