Steroid-Free Deep Remission at One Year Does Not Prevent Crohn's Disease Progression: Long-Term Data From the TAILORIX Trial.


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:
09 2022
Historique:
received: 14 09 2021
revised: 14 11 2021
accepted: 18 11 2021
pubmed: 30 11 2021
medline: 31 8 2022
entrez: 29 11 2021
Statut: ppublish

Résumé

Crohn's disease (CD) patients included in the Tailored Treatment With Infliximab for Active Crohn's Disease (TAILORIX) trial started infliximab in combination with an immunosuppressant for 1 year. The aim of the present study was to determine the long-term disease course beyond the study period. We compared the outcomes of patients who did or did not reach the primary end point of the TAILORIX trial, defined as sustained corticosteroid-free clinical remission from weeks 22 through 54, with no ulcers on ileocolonoscopy at week 54. The primary outcome of this follow-up study was the progression-free survival of CD defined by anal or major abdominal surgery, CD-related hospitalization, or the need for a new systemic CD treatment. The 95 patients (median disease duration, 4.5 mo; interquartile range, 1.0-56.6 mo) analyzed, including 45 (47%) who achieved the primary end point, were followed up for a median duration of 64.2 months (interquartile range, 57.6-69.9 mo) after the end of the study period. There was no significant difference in CD progression-free survival at 1, 3, and 5 years between patients who achieved the TAILORIX primary end point and patients who did not (P = .64). No difference was observed between both groups for each component of CD progression: anal surgery, major abdominal surgery, CD-related hospitalization, or the need for a new systemic CD treatment. Achieving a sustained clinical remission off steroids with complete endoscopic remission in this cohort of 95 patients with early CD was not associated with less disease progression. Prospective trials to define the therapeutic goals that change the natural history of CD and prevent complications are needed.

Sections du résumé

BACKGROUND & AIMS
Crohn's disease (CD) patients included in the Tailored Treatment With Infliximab for Active Crohn's Disease (TAILORIX) trial started infliximab in combination with an immunosuppressant for 1 year. The aim of the present study was to determine the long-term disease course beyond the study period.
METHODS
We compared the outcomes of patients who did or did not reach the primary end point of the TAILORIX trial, defined as sustained corticosteroid-free clinical remission from weeks 22 through 54, with no ulcers on ileocolonoscopy at week 54. The primary outcome of this follow-up study was the progression-free survival of CD defined by anal or major abdominal surgery, CD-related hospitalization, or the need for a new systemic CD treatment.
RESULTS
The 95 patients (median disease duration, 4.5 mo; interquartile range, 1.0-56.6 mo) analyzed, including 45 (47%) who achieved the primary end point, were followed up for a median duration of 64.2 months (interquartile range, 57.6-69.9 mo) after the end of the study period. There was no significant difference in CD progression-free survival at 1, 3, and 5 years between patients who achieved the TAILORIX primary end point and patients who did not (P = .64). No difference was observed between both groups for each component of CD progression: anal surgery, major abdominal surgery, CD-related hospitalization, or the need for a new systemic CD treatment.
CONCLUSIONS
Achieving a sustained clinical remission off steroids with complete endoscopic remission in this cohort of 95 patients with early CD was not associated with less disease progression. Prospective trials to define the therapeutic goals that change the natural history of CD and prevent complications are needed.

Identifiants

pubmed: 34843987
pii: S1542-3565(21)01268-4
doi: 10.1016/j.cgh.2021.11.030
pii:
doi:

Substances chimiques

Steroids 0
Infliximab B72HH48FLU

Types de publication

Clinical Trial Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

2074-2082

Commentaires et corrections

Type : CommentIn

Informations de copyright

Copyright © 2022 AGA Institute. Published by Elsevier Inc. All rights reserved.

Auteurs

David Laharie (D)

Centre Hospitalier Universitaire de Bordeaux, Hôpital Haut-Lévêque, Service d'Hépato-gastroentérologie et Oncologie Digestive, Université de Bordeaux, Bordeaux, France. Electronic address: david.laharie@chu-bordeaux.fr.

Geert D'Haens (G)

Hepato-Gastroenterology Department, Amsterdam University Medical Centers, Amsterdam, The Netherlands.

Maria Nachury (M)

Hepato-Gastroenterology Department, Claude Huriez Hospital, University of Lille, Lille, France.

Guy Lambrecht (G)

Gastroenterology Unit, Damiaan Hospital, Oostende, Belgium.

Peter Bossuyt (P)

Imelda Gastronintestinal Clinical Research Center, Department of Gastroenterology, Imelda General Hospital, Bonheiden, Belgium.

Yoram Bouhnik (Y)

Hepato-Gastroenterology Department, Beaujon Hospital.

Edouard Louis (E)

Gastroenterology Department, University Hospital, CHU Liège, Liège, Belgium.

Christien Janneke van der Woude (C)

Department of Gastroenterology and Hepatology, Erasmus MC, Rotterdam, The Netherlands.

Anthony Buisson (A)

Hepato-Gastroenterology Department, Hospital Estaing, Clermont-Ferrand, France.

Philippe Van Hootegem (P)

Department of Gastroenterology, Sint-Lucas General Hospital, Brugge, Belgium.

Matthieu Allez (M)

Hepato-Gastroenterology Department, Saint-Louis Hospital, University of Paris VII, Paris, France.

Jérôme Filippi (J)

Department of Gastroenterology, Hôpital L'Archet, Nice, France.

Hedia Brixi (H)

CHU Robert Debré, Service d'Hépato-gastroentérologie et Oncologie Digestive, Reims, France.

Cyrielle Gilletta (C)

Department of Gastroenterology and Pancreatology, CHU de Toulouse, Toulouse, France.

Laurence Picon (L)

Department of Gastroenterology, Centre Hospitalier Regional Universitaire de Tours, Tours, France.

Filip Baert (F)

AZ Delta, Roeselare, Belgium.

Séverine Vermeire (S)

University Hospitals Leuven, Katholieke Universiteit Leuven, Leuven, Belgium.

Nicolas Duveau (N)

Hepato-Gastroenterology Department, Roubaix Hospital, Roubaix, France.

Laurent Peyrin-Biroulet (L)

Department of Gastroenterology, Inserm U1256, Nancy University Hospital, Lorraine University, Vandoeuvre-les-Nancy, France.

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Classifications MeSH