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Real‐world comparison of effectiveness between tofacitinib and vedolizumab in patients with ulcerative colitis exposed to at least one anti‐ TNF agent

Authors :
Anthony Buisson
Maria Nachury
Thomas Guilmoteau
Romain Altwegg
Xavier Treton
Mathurin Fumery
Melanie Serrero
Eloïse Leclerc
Ludovic Caillo
Bruno Pereira
Aurélien Amiot
Guillaume Bouguen
Microbes, Intestin, Inflammation et Susceptibilité de l'Hôte (M2iSH)
Institut National de la Santé et de la Recherche Médicale (INSERM)-Centre de Recherche en Nutrition Humaine d'Auvergne (CRNH d'Auvergne)-Institut National de Recherche pour l’Agriculture, l’Alimentation et l’Environnement (INRAE)-Université Clermont Auvergne (UCA)
Service d'Hépatologie Gastro-entérologie [CHU Clermont-Ferrand]
CHU Estaing [Clermont-Ferrand]
CHU Clermont-Ferrand-CHU Clermont-Ferrand
Infection Inflammation et Interaction Hôtes Pathogènes [CHU Clermont-Ferrand] (3IHP )
Direction de la recherche clinique et de l’innovation [CHU Clermont-Ferrand] (DRCI)
Institute for Translational Research in Inflammation - U 1286 (INFINITE (Ex-Liric))
Institut National de la Santé et de la Recherche Médicale (INSERM)-Université de Lille-Centre Hospitalier Régional Universitaire [Lille] (CHRU Lille)
Hôpital Saint Eloi (CHRU Montpellier)
Centre Hospitalier Régional Universitaire [Montpellier] (CHRU Montpellier)
Service de Gastroentérologie [Hôpital Beaujon]
Hôpital Beaujon [AP-HP]
Assistance publique - Hôpitaux de Paris (AP-HP) (AP-HP)-Assistance publique - Hôpitaux de Paris (AP-HP) (AP-HP)
Périnatalité et Risques Toxiques - UMR INERIS_I 1 (PERITOX)
Institut National de l'Environnement Industriel et des Risques (INERIS)-Université de Picardie Jules Verne (UPJV)-CHU Amiens-Picardie
Hôpital Nord [CHU - APHM]
Hôpital Universitaire Carémeau [Nîmes] (CHU Nîmes)
Centre Hospitalier Universitaire de Nîmes (CHU Nîmes)
Unité de Biostatistiques [CHU Clermont-Ferrand]
Early detection of Colon Cancer using Molecular Markers and Microbiota (EA 7375) (EC2M3)
Université Paris-Est Créteil Val-de-Marne - Paris 12 (UPEC UP12)
Nutrition, Métabolismes et Cancer (NuMeCan)
Université de Rennes 1 (UR1)
Université de Rennes (UNIV-RENNES)-Université de Rennes (UNIV-RENNES)-Institut National de la Santé et de la Recherche Médicale (INSERM)-Institut National de Recherche pour l’Agriculture, l’Alimentation et l’Environnement (INRAE)
Centre d'Investigation Clinique [Rennes] (CIC)
Université de Rennes (UNIV-RENNES)-Université de Rennes (UNIV-RENNES)-Hôpital Pontchaillou-Institut National de la Santé et de la Recherche Médicale (INSERM)
Pfilzer
Université de Rennes (UR)-Institut National de la Santé et de la Recherche Médicale (INSERM)-Institut National de Recherche pour l’Agriculture, l’Alimentation et l’Environnement (INRAE)
Université de Rennes (UR)-Hôpital Pontchaillou-Institut National de la Santé et de la Recherche Médicale (INSERM)
Source :
Alimentary Pharmacology & Therapeutics (Suppl), Alimentary Pharmacology & Therapeutics (Suppl), 2022, pp.1-13. ⟨10.1111/apt.17305⟩
Publication Year :
2022
Publisher :
HAL CCSD, 2022.

Abstract

International audience; Background: Data comparing tofacitinib and vedolizumab in ulcerative colitis (UC) are lacking.Aims: To compare the effectiveness of tofacitinib and vedolizumab in patients with UC who had prior exposure to anti-TNF therapy METHODS: In this multicentre study, we included consecutive patients with UC ≥18 years old with partial Mayo score >2 and prior anti-TNF exposure, who started tofacitinib or vedolizumab between January 2019 and June 2021. Comparisons were performed using propensity score analyses (inverse probability of treatment weighting).Results: Overall, 126 and 178 patients received tofacitinib and vedolizumab, respectively. Intensified induction (vedolizumab infusion at week 10 or tofacitinib 10 mg b.d until week 16) was performed in 28.5% and 41.5% of patients, respectively. After propensity-score analysis, corticosteroid-free clinical remission (partial Mayo score ≤2) was achieved at week 16 in 45.1% and 40.2% of patients receiving tofacitinib and vedolizumab, respectively (aOR = 0.82 [0.35-1.91], p = 0.64). Endoscopic improvement (corticosteroid-free clinical remission and endoscopic Mayo score ≤1) (aOR = 0.23[0.08-0.65], p = 0.0032) and histological healing (endoscopic improvement + Nancy histological index ≤1) (13.4% vs 3.2%, aOR = 0.21[0.05-0.91], p = 0.023) were higher at week 16 in patients treated with tofacitinib. No factor was predictive of tofacitinib effectiveness. At least one primary failure to a biologic (OR = 0.46[0.22-0.99], p = 0.049), partial Mayo score >6 (OR = 0.39[0.17-0.90], p = 0.029) and CRP level > 30 mg/L at baseline (OR = 0.08[0.01-0.85], p = 0.036) were associated with vedolizumab failure.Conclusion: Tofacitinib and vedolizumab are effective in UC after failure of anti-TNF agents. However, tofacitinib seems more effective, especially in severe disease and primary failure to biologics.

Details

Language :
English
ISSN :
09530673 and 13652036
Database :
OpenAIRE
Journal :
Alimentary Pharmacology & Therapeutics (Suppl), Alimentary Pharmacology & Therapeutics (Suppl), 2022, pp.1-13. ⟨10.1111/apt.17305⟩
Accession number :
edsair.doi.dedup.....9f3a5683f37e16e31d49503f0c268f8d
Full Text :
https://doi.org/10.1111/apt.17305⟩