Complete Endoscopic Healing Is Associated With Lower Relapse Risk After Anti-TNF Withdrawal in Inflammatory Bowel Disease.


Journal

Clinical gastroenterology and hepatology : the official clinical practice journal of the American Gastroenterological Association
ISSN: 1542-7714
Titre abrégé: Clin Gastroenterol Hepatol
Pays: United States
ID NLM: 101160775

Informations de publication

Date de publication:
Mar 2023
Historique:
received: 16 04 2022
revised: 11 08 2022
accepted: 15 08 2022
pubmed: 3 9 2022
medline: 3 3 2023
entrez: 2 9 2022
Statut: ppublish

Résumé

Discontinuation of anti-tumor necrosis factor-α treatment (anti-TNF) (infliximab and adalimumab) in patients with inflammatory bowel disease (IBD) is associated with a high relapse risk that may be influenced by endoscopic activity at the time of stopping. We assessed the relapse rate after anti-TNF withdrawal in patients with endoscopic healing and studied predictors of relapse including the depth of endoscopic healing. This was a multicenter, prospective study in adult patients with Crohn's disease (CD), ulcerative colitis (UC), or IBD-unclassified (IBDU), with ≥6 months of corticosteroid-free clinical remission (confirmed at baseline) and endoscopic healing (Mayo <2/SES-CD <5 without large ulcers), who discontinued anti-TNF between 2018 and 2020 in the Netherlands. We performed Kaplan-Meier and Cox regression analyses to assess the relapse rate and evaluate potential predictors: partial (Mayo 1/SES-CD 3-4) versus complete (Mayo 0/SES-CD 0-2) endoscopic healing, anti-TNF trough levels, and immunomodulator and/or mesalamine use. Among 81 patients (CD: n = 41, 51%) with a median follow-up of 2.0 years (interquartile range, 1.6-2.1), 40 patients (49%) relapsed. Relapse rates in CD and UC/IBDU patients were comparable. At 12 months, 70% versus 35% of patients with partial versus complete endoscopic healing relapsed, respectively (adjusted hazard rate [aHR], 3.28; 95% confidence interval [CI], 1.43-7.50). Mesalamine use was associated with fewer relapses in UC/IBDU patients (aHR, 0.08; 95% CI, 0.01-0.67). Thirty patients restarted anti-TNF, and clinical remission was regained in 73% at 3 months. The relapse risk was high after anti-TNF withdrawal in IBD patients with endoscopic healing, but remission was regained in most cases after anti-TNF reintroduction. Complete endoscopic healing and mesalamine treatment in UC/IBDU patients decreased the risk of relapse.

Sections du résumé

BACKGROUND & AIMS OBJECTIVE
Discontinuation of anti-tumor necrosis factor-α treatment (anti-TNF) (infliximab and adalimumab) in patients with inflammatory bowel disease (IBD) is associated with a high relapse risk that may be influenced by endoscopic activity at the time of stopping. We assessed the relapse rate after anti-TNF withdrawal in patients with endoscopic healing and studied predictors of relapse including the depth of endoscopic healing.
METHODS METHODS
This was a multicenter, prospective study in adult patients with Crohn's disease (CD), ulcerative colitis (UC), or IBD-unclassified (IBDU), with ≥6 months of corticosteroid-free clinical remission (confirmed at baseline) and endoscopic healing (Mayo <2/SES-CD <5 without large ulcers), who discontinued anti-TNF between 2018 and 2020 in the Netherlands. We performed Kaplan-Meier and Cox regression analyses to assess the relapse rate and evaluate potential predictors: partial (Mayo 1/SES-CD 3-4) versus complete (Mayo 0/SES-CD 0-2) endoscopic healing, anti-TNF trough levels, and immunomodulator and/or mesalamine use.
RESULTS RESULTS
Among 81 patients (CD: n = 41, 51%) with a median follow-up of 2.0 years (interquartile range, 1.6-2.1), 40 patients (49%) relapsed. Relapse rates in CD and UC/IBDU patients were comparable. At 12 months, 70% versus 35% of patients with partial versus complete endoscopic healing relapsed, respectively (adjusted hazard rate [aHR], 3.28; 95% confidence interval [CI], 1.43-7.50). Mesalamine use was associated with fewer relapses in UC/IBDU patients (aHR, 0.08; 95% CI, 0.01-0.67). Thirty patients restarted anti-TNF, and clinical remission was regained in 73% at 3 months.
CONCLUSIONS CONCLUSIONS
The relapse risk was high after anti-TNF withdrawal in IBD patients with endoscopic healing, but remission was regained in most cases after anti-TNF reintroduction. Complete endoscopic healing and mesalamine treatment in UC/IBDU patients decreased the risk of relapse.

Identifiants

pubmed: 36055567
pii: S1542-3565(22)00820-5
doi: 10.1016/j.cgh.2022.08.024
pii:
doi:

Substances chimiques

Tumor Necrosis Factor Inhibitors 0
Mesalamine 4Q81I59GXC
Infliximab B72HH48FLU

Types de publication

Multicenter Study Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

750-760.e4

Informations de copyright

Copyright © 2023 The Authors. Published by Elsevier Inc. All rights reserved.

Auteurs

Remi Mahmoud (R)

Department of Gastroenterology and Hepatology, University Medical Center Utrecht, Utrecht, The Netherlands.

Edo H J Savelkoul (EHJ)

Department of Gastroenterology and Hepatology, Radboud University Medical Center, Nijmegen, The Netherlands.

Wout Mares (W)

Department of Gastroenterology and Hepatology, Gelderse Vallei Hospital, Ede, The Netherlands.

Rogier Goetgebuer (R)

Department of Gastroenterology and Hepatology, Erasmus University Medical Center, Rotterdam, The Netherlands; Department of Gastroenterology and Hepatology, Amsterdam University Medical Center, Amsterdam, The Netherlands.

Ben J M Witteman (BJM)

Department of Gastroenterology and Hepatology, Gelderse Vallei Hospital, Ede, The Netherlands.

Daan B de Koning (DB)

Department of Gastroenterology and Hepatology, Gelre Hospital, Apeldoorn, The Netherlands.

Sebastiaan A C van Tuyl (SAC)

Department of Gastroenterology and Hepatology, Diakonessenhuis, Utrecht, The Netherlands.

Itta Minderhoud (I)

Department of Gastroenterology and Hepatology, Tergooi Medical Center, Hilversum, The Netherlands.

Maurice W M D Lutgens (MWMD)

Department of Gastroenterology and Hepatology, Elisabeth-TweeSteden Hospital, Tilburg, The Netherlands.

Dilek Akol-Simsek (D)

Department of Gastroenterology and Hepatology, DC klinieken, Apeldoorn, The Netherlands.

Fiona D M van Schaik (FDM)

Department of Gastroenterology and Hepatology, University Medical Center Utrecht, Utrecht, The Netherlands.

Herma H Fidder (HH)

Department of Gastroenterology and Hepatology, University Medical Center Utrecht, Utrecht, The Netherlands.

Jeroen M Jansen (JM)

Department of Gastroenterology and Hepatology, Onze Lieve Vrouwe Gasthuis (OLVG), Amsterdam, The Netherlands.

Petra G A van Boeckel (PGA)

Department of Gastroenterology and Hepatology, St Antonius Hospital, Nieuwegein, The Netherlands.

Nofel Mahmmod (N)

Department of Gastroenterology and Hepatology, St Antonius Hospital, Nieuwegein, The Netherlands.

Carmen S Horjus-Talabur Horje (CS)

Department of Gastroenterology and Hepatology, Rijnstate Hospital, Arnhem, The Netherlands.

Tessa E H Römkens (TEH)

Department of Gastroenterology and Hepatology, Jeroen Bosch Hospital, 's-Hertogenbosch, The Netherlands.

Jean-Frédéric Colombel (JF)

Department of Medicine, Division of Gastroenterology, Icahn School of Medicine at Mount Sinai, New York City, New York.

Frank Hoentjen (F)

Department of Gastroenterology and Hepatology, Radboud University Medical Center, Nijmegen, The Netherlands; Division of Gastroenterology, Department of Medicine, University of Alberta, Edmonton, Canada.

Bindia Jharap (B)

Department of Gastroenterology and Hepatology, Meander Medical Center, Amersfoort, The Netherlands.

Bas Oldenburg (B)

Department of Gastroenterology and Hepatology, University Medical Center Utrecht, Utrecht, The Netherlands. Electronic address: boldenbu@umcutrecht.nl.

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