New-onset inflammatory bowel diseases among IL-17 inhibitor-treated patients: results from the case-control MISSIL study.


Journal

Rheumatology (Oxford, England)
ISSN: 1462-0332
Titre abrégé: Rheumatology (Oxford)
Pays: England
ID NLM: 100883501

Informations de publication

Date de publication:
06 07 2022
Historique:
received: 31 08 2021
revised: 29 10 2021
pubmed: 4 11 2021
medline: 9 7 2022
entrez: 3 11 2021
Statut: ppublish

Résumé

To describe new-onset IBD (new IBD) in patients treated with IL-17 inhibitors (IL-17i), to assess their incidence and to identify their risk factors in real life. A French national registry (MISSIL) aimed to report all cases of new IBD in patients treated with IL-17i from January 2016 to December 2019. Using the estimated number of patients treated by IL-17 in France during the study period, the annual incidence rates of new IBD was reported in IL-17i-treated patients. A case-control study was performed with two controls per new IBD case matched by gender, age and underlying inflammatory disease. Thirty-one cases of new IBD under IL-17i were collected: 27 patients treated for spondyloarthritis and four patients for psoriasis. All were observed with secukinumab (SEK). The median time to onset of new IBD symptoms was 4.0 (1.5-7.5) months. SEK was discontinued in all patients. The evolution was favourable with complete resolution (17/31), improvement (7/31) or stabilization (5/31). Two patients died: one due to a massive myocardial infarction and one due to post-colectomy complications. The incidence of new IBD decreased from 0.69/100 patient-years [PY] (7/1010) in 2016 to 0.08/100 PY (6/7951) in 2019. No previous treatment with etanercept (odds ratio [OR] = 0.33, 95% CI: 0.14-0.80, P = 0.014) and low number of previous biologic therapies (OR = 0.67, 95% CI: 0.47, 0.94, P = 0.021) were significantly associated with new IBD. The incidence of new IBD was low and decreased from 2016 to 2019. The outcome was favourable in 24 out of 31 patients, but two patients died.

Identifiants

pubmed: 34730790
pii: 6420221
doi: 10.1093/rheumatology/keab819
doi:

Substances chimiques

Interleukin-17 0
Etanercept OP401G7OJC

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

2848-2855

Informations de copyright

© The Author(s) 2021. Published by Oxford University Press on behalf of the British Society for Rheumatology. All rights reserved. For permissions, please email: journals.permissions@oup.com.

Auteurs

Jean-Guillaume Letarouilly (JG)

Service de Rhumatologie, Université de Lille, CHU Lille, Lille.

Thao Pham (T)

Service de Rhumatologie, Aix Marseille University, APHM, Marseille.

Adeline Pierache (A)

Université de Lille, CHU Lille, ULR 2694-METRICS: évaluation des technologies de santé et des pratiques médicales, Lille.
Département des Biostatistiques, CHU de Lille, Lille, France.

Émilie Acquacalda (É)

Service de Rhumatologie, Princess Grace Hospital Centre, Monaco, Monaco.

Béatrice Banneville (B)

Service de Rhumatologie, University Hospital Pitié Salpêtrière, APHP, Paris.

Sébastien Barbarot (S)

Université de Nantes, CHU Nantes, Service de Dermatologie, UMR 1280 PhAN, INRAE, Nantes.

Pauline Baudart (P)

Service de Rhumatologie, CHU Caen, Caen.

Élodie Bauer (É)

Service de Rhumatologie, CHU de Nancy, Nancy.

Pascal Claudepierre (P)

Service de Rhumatologie, Université Paris Est Créteil Val de Marne, EA 7379-Epiderme, AP-HP, Hôpital Henri-Mondor, Créteil.

Arnaud Constantin (A)

Service de Rhumatologie, CHU Toulouse, Toulouse.

Emmanuelle Dernis (E)

Service de Rhumatologie, CH Le Mans, Le Mans.

Renaud Felten (R)

CHU de Strasbourg, Service de rhumatologie, Département Universitaire de Pharmacologie, Addictologie, Toxicologie et Thérapeutique, Université de Strasbourg, Strasbourg.

Philippe Gaudin (P)

Service de Rhumatologie, CHU Grenoble Alpes, Grenoble.

Céline Girard (C)

Service de Dermatologie, CHU Montpellier, Montpellier.

Bruno Gombert (B)

Service de Rhumatologie, CH La Rochelle, La Rochelle.

Philippe Goupille (P)

Service de Rhumatologie, CHU de Tours, Tours.

Xavier Guennoc (X)

Service de Rhumatologie, Centre Hospitalier de Saint-Brieuc, Saint-Brieuc.

Isabelle Henry-Desailly (I)

Service de Rhumatologie, Centre Hospitalier Universitaire Amiens-Picardie, Amiens.

Denis Jullien (D)

CHU Lyon, Service de dermatologie, Hôpital Edouard Herriot, Lyon.

Elena Karimova (E)

Service de Dermatologie, CH Lens, Lens.

Sylvain Lanot (S)

Service de Rhumatologie, Centre Hospitalier Intercommunal Alençon-Mamers, Alençon.

Loïc Le Dantec (L)

Service de Rhumatologie, Polyclinique d'Henin-Beaumont, Hénin-Beaumont.

Tristan Pascart (T)

Service de Rhumatologie, GHICL, Hôpital Saint-Philibert, Lomme.

Laurianne Plastaras (L)

Service de Gastroentérologie, CH Colmar, Colmar.

Nathalie Sultan (N)

CH Ouest-Réunion, Saint-Paul, La Réunion.

Xavier Truchet (X)

Service de Pathologies Digestives, HIA Sainte Anne, Toulon.

Stéphane Varin (S)

Service de Rhumatologie, CHD Vendée, La Roche-sur-Yon.

Daniel Wendling (D)

CHU Besançon, Service de rhumatologie, EA 4266, Université de Franche-Comté, Besançon.

Louise Gaboriau (L)

Centre Régional de Pharmacovigilance, Service de Pharmacologie Médicale, CHU de Lille.

Delphine Staumont-Sallé (D)

Université de Lille, CHU Lille, Service de dermatologie, U1286 Inserm INFINITE, Lille.

Laurent Peyrin-Biroulet (L)

Service de Gastroentérologie, CHU de Nancy, Nancy, France.

René-Marc Flipo (RM)

Service de Rhumatologie, Université de Lille, CHU Lille, Lille.

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Classifications MeSH