Tofacitinib for Patients with Anti-TNF Refractory Ulcerative Proctitis: A Multicentre Cohort Study from the GETAID.

Aurélien Amiot, Guillaume Le Cosquer, Maeva Charkaoui, Laurent Peyrin-Biroulet, Mathurin Fumery, Guillaume Bouguen, Guillaume Savoye, Mathias Vidon, Maria Nachury, Bénédicte Caron, Mathieu Uzzan, Alban Benezech, Lucas Guillo, Yoram Bouhnik, Alexandre Nuzzo, Catherine Le Berre, Julien Kirchgesner, Anthony Buisson, Catherine Reenaers

Journal: Journal of Crohn's & colitis 2024;18(3):424-430

PMID: 37796025

Abstract

BACKGROUND

Although ulcerative proctitis [UP] can dramatically impair quality of life, treatment efficacy has been poorly investigated in UP as it was historically excluded from phase 2/3 randomised controlled trials in ulcerative colitis. Our aim was to assess the effectiveness and safety of tofacitinib for the treatment of UP.

METHODS

We conducted a retrospective, multicentre study in 17 GETAID centres, including consecutive patients with UP treated with tofacitinib. The primary endpoint was steroid-free remission between Week 8 and Week 14, defined as a partial Mayo score of 2 [and no individual subscore above 1]. Secondary outcomes included clinical response and steroid-free remission after induction and at 1 year.

RESULTS

All the 35 enrolled patients previously received anti-tumour necrosis factor [TNF] therapy and 88.6% were exposed to at least two lines of biologics. At baseline, the median partial Mayo score was 7 (intequartile range [IQR] [5.5-7]). After induction [W8-W14], 42.9% and 60.0% of patients achieved steroid-free remission and clinical response, respectively. At 1 year, the steroid-free clinical remission and clinical response rates were 39.4% and 45.5%, respectively, and 51.2% [17/33] were still receiving tofacitinib treatment. Survival without tofacitinib withdrawal was estimated at 50.4% (95% confidence interval [CI] [35.5-71.6]) at 1 year. Only a lower partial Mayo at baseline was independently associated with remission at induction (0dds ratio [OR] = 0.56 for an increase of 1, (95% CI [0.33-0.95], p = 0.03). Five [14.3%] adverse events were reported, with one leading to treatment withdrawal [septic shock secondary to cholecystitis].

CONCLUSION

Tofacitinib may offer a therapeutic option for patients with refractory UP.

© The Author(s) 2023. Published by Oxford University Press on behalf of European Crohn’s and Colitis Organisation. All rights reserved. For permissions, please email: [email protected].

Address: University of Lille, CHU Lille, Institute for Translational Research in Inflammation, Lille, France.; Department of Gastroenterology, Hopital Beaujon, Universite de Paris, France.; Department of Gastroenterology, Hopitaux Universitaires Bicêtre, Universite Paris Est Creteil and Universite Paris Saclay, Centre for Research in Epidemiology and Population Health, Le Kremlin Bicêtre, France.; Department of Gastroenterology, Nancy University Hospital, and INSERM, NGERE, University of Lorraine, Nancy, France.; Department of Gastroenterology, Centre Hospitalier Avignon, Avignon, France.; Université Clermont Auvergne, Service d'Hépato-Gastroentérologie, Clermont-Ferrand, France.; Department of Gastroenterology, CHU Renes, Renes, France.; Institut des Maladies de l'Appareil Digestif, Hépato-Gastro-Entérologie et Assistance Nutritionnelle,Nantes Université, Nantes, France.; Department of Gastroenterology and Hepatology, CHU Liège, University of Liège, Liège, Belgium.; Department of Gastroenterology and Pancreatology, Hôpital Rangueil, Université Toulouse Paul Sabatier, Toulouse, France.; Department of Gastroenterology Rouen University Hospital, UMR 1073 University of Rouen Normandy, Rouen, France.; Department of Hepatogastroenterology, Dijon University Hospital, Dijon, France.; Department of Gastroenterology. Hopital Intercommunal de Créteil, Créteil, France.; Department of Gastroenterology, University Hospital of Marseille Nord, University of Aix-Marseille, Marseille, France.; Department of Gastroenterology, Amiens University Hospital, and UMR I01, PERITOX, Jules Verne University of Picardy, Amiens, France.; Institut Pierre Louis d'Epidémiologie et de Santé Publique, Sorbonne Université, Department of Gastroenterology, Hôpital Saint-Antoine, Paris, France.; Paris IBD Center, Groupe Hospitalier Privé Ambroise Paré - Hartmann, Neuilly sur Seine, France.
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