Treatment of antibiotic refractory chronic pouchitis with JAK inhibitors and S1P receptor modulators: an ECCO CONFER Multicentre Case Series.

biologics filgotinib ozanimod pouchitis small molecules target therapy tofacitinib ulcerative colitis upadacitinib

Journal

Journal of Crohn's & colitis
ISSN: 1876-4479
Titre abrégé: J Crohns Colitis
Pays: England
ID NLM: 101318676

Informations de publication

Date de publication:
15 Nov 2023
Historique:
received: 10 10 2023
medline: 15 11 2023
pubmed: 15 11 2023
entrez: 15 11 2023
Statut: aheadofprint

Résumé

Data regarding effectiveness and safety of JAK inhibitors and S1P receptor modulators in antibiotic refractory chronic pouchitis (CARP) are lacking. This ECCO-CONFER project retrospectively collected JAK inhibitors or S1P receptor modulators treatments for CARP with at least 3-months follow up. The outcomes included corticosteroid and antibiotics-free clinical response and remission at three and twelve months, trend in mPDAI, endoscopic PDAI, CRP and calprotectin. Seventeen treatments in 15 patients were collected. Previous pouchitis treatments included infliximab (5/15), adalimumab (4/15), vedolizumab (9/15), and ustekinumab (5/15). Pooling data on JAK inhibitors (8 tofacitinib, 1 filgotinib and 6 upadacitinib), after 3 months (T3), steroid and antibiotics-free clinical response was achieved in 53.3% (8/15), steroid and antibiotics-free clinical remission was achieved in 40% (6/15). Of the patients with at least 12 months of follow-up, steroid and antibiotics-free clinical response was achieved in 50% (3/6) and remission in one patient (16.7%), endoscopic response in 50% (3/6), endoscopic remission in 50% (3/6). Of the two ozanimod treatments at T3, steroid and antibiotics-free clinical response was achieved in one patient, without remission; both discontinued ozanimod before T12. No side effects reported. Small molecules may represent a suitable option for CARP refractory to multiple biologics, deserving further investigation.

Sections du résumé

BACKGROUND AND AIMS OBJECTIVE
Data regarding effectiveness and safety of JAK inhibitors and S1P receptor modulators in antibiotic refractory chronic pouchitis (CARP) are lacking.
METHODS METHODS
This ECCO-CONFER project retrospectively collected JAK inhibitors or S1P receptor modulators treatments for CARP with at least 3-months follow up. The outcomes included corticosteroid and antibiotics-free clinical response and remission at three and twelve months, trend in mPDAI, endoscopic PDAI, CRP and calprotectin.
RESULTS RESULTS
Seventeen treatments in 15 patients were collected. Previous pouchitis treatments included infliximab (5/15), adalimumab (4/15), vedolizumab (9/15), and ustekinumab (5/15). Pooling data on JAK inhibitors (8 tofacitinib, 1 filgotinib and 6 upadacitinib), after 3 months (T3), steroid and antibiotics-free clinical response was achieved in 53.3% (8/15), steroid and antibiotics-free clinical remission was achieved in 40% (6/15). Of the patients with at least 12 months of follow-up, steroid and antibiotics-free clinical response was achieved in 50% (3/6) and remission in one patient (16.7%), endoscopic response in 50% (3/6), endoscopic remission in 50% (3/6). Of the two ozanimod treatments at T3, steroid and antibiotics-free clinical response was achieved in one patient, without remission; both discontinued ozanimod before T12. No side effects reported.
CONCLUSIONS CONCLUSIONS
Small molecules may represent a suitable option for CARP refractory to multiple biologics, deserving further investigation.

Identifiants

pubmed: 37965867
pii: 7420584
doi: 10.1093/ecco-jcc/jjad194
pii:
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Informations de copyright

© 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: journals.permissions@oup.com.

Auteurs

Davide Giuseppe Ribaldone (DG)

Department of Medical Sciences, Division of Gastroenterology, University of Turin, Turin, Italy.

Giulia Testa (G)

Gastroenterology-U, A.O.U. Città della Salute e della Scienza di Torino, Turin, Italy.

Bram Verstockt (B)

Department of Gastroenterology and Hepatology, University Hospitals Leuven, KU Leuven, Leuven, Belgium.
Department of Chronic Diseases and Metabolism, KU Leuven, Leuven, Belgium.

Tamas Molnar (T)

University of Szeged, Hungary.

Edoardo Savarino (E)

Division of Gastroenterology, Department of Surgery Oncology and Gastroenterology DiSCOG, University of Padova, Padova, Italy.

Carsten Schmidt (C)

Medical Clinic II, Hospital Fulda, Fulda, Germany.
Medical Faculty of the Friedrich Schiller University, Jena, Germany.

Sophie Vieujean (S)

Hepato-Gastroenterology and Digestive Oncology, University Hospital CHU of Liège, Liège, Belgium.

Niels Teich (N)

Medical Faculty of the Friedrich Schiller University, Jena, Germany.
Gastroenterology Practice, Leipzig, Germany.

Corina Meianu (C)

Faculty of Medicine, Carol Davila University of Medicine and Pharmacy, 050474 Bucharest, Romania.
Gastroenterology Department, Fundeni Clinical Institute, 022328 Bucharest, Romania.

Pascal Juillerat (P)

Clinic for Visceral Surgery and Medicine, Department of Gastroenterology, Bern University Hospital.
Crohn and Colitis Center, Gastro-enterologie Beaulieu SA, Lausanne, Switzerland.

Nathan Grellier (N)

Hepato-Gastroenterology Department, University Hospital of Poitiers, Poitiers, France.

Triana Lobaton (T)

Department of Internal Medicine and Pediatrics, Ghent University, Ghent, Belgium; Department of Gastroenterology, University Hospital Ghent, Ghent, Belgium.

Classifications MeSH