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P766 No difference in progression of disability 2 years after stopping infliximab or immunosuppressant vs. continuing combination therapy in patients with CD in sustained steroid-free remission: a subanalysis of SPARE

Title: P766 No difference in progression of disability 2 years after stopping infliximab or immunosuppressant vs. continuing combination therapy in patients with CD in sustained steroid-free remission: a subanalysis of SPARE
Authors: Vieujean, S; Desseaux, K; Laharie, D; Satsangi, J; Ding, N; Siegmund, B; D’Haens, G; Picon, L; Bossuyt, P; Vuitton, L; Irving, P; Viennot, S; Lamb, C A; Pollok, R; Baert, F; Nachury, M; Fumery, M; Gilletta, C; Resche-Rigon, M; Bouhnik, Y; Colombel, J F; Hertervig, E; Louis, E
Source: Journal of Crohn's and Colitis ; volume 18, issue Supplement_1, page i1419-i1421 ; ISSN 1873-9946 1876-4479
Publisher Information: Oxford University Press (OUP)
Publication Year: 2024
Description: Background In the SPARE trial, the discontinuation of infliximab (IFX) in patients with Crohn’s disease (CD) in sustained remission under combination therapy (IFX and immunosuppressant therapy), was associated with a significantly higher relapse rate than when continuing combination therapy or discontinuing immunosuppressant therapy. However, a high proportion of patients rapidly recover remission when resuming treatment. The impact of this treatment strategy on functional disability, a major endpoint in assessing CD progression, has been poorly studied. We aimed to compare the evolution of the IBD-disability index (IBD-DI) in patients continuing combination therapy, discontinuing IFX or immunosuppressant therapy. Methods The study of the evolution of the IBD-DI in the 3 groups (combination, IFX withdrawal, immunosuppressant withdrawal), between baseline and the end of study (2 years), was a pre-defined secondary endpoint of the trial. Changes in scores (between baseline and the end of study) were compared using Wilcoxon tests between the arms “combination group” versus “IFX withdrawal group” and between “immunosuppressant withdrawal group” versus “IFX withdrawal group”. Results IBD-DI was available at baseline and at the end of study for 153 patients out of the 211 randomised in the SPARE trial between November 2015 and April 2019 (46 in the combination group, 55 in the IFX withdrawal group, and 52 in the immunosuppressant withdrawal group) and those were included in the analysis. Table 1 summarizes baseline characteristics of these patients. 30 patients had a relapse (6 [13%] of 46 in the combination group, 19 [34.5%] of 55 in the IFX withdrawal group, 5 [9.6%] of 52 in the immunosuppressant withdrawal group). Of 23 patients who had a relapse and were retreated or optimised according to protocol, remission was achieved in 21 patients (1 of 2 in the combination group, 18 of 19 in the IFX withdrawal group, and 2 of 2 in the immunosuppressant withdrawal group). The median IBD-DI at baseline was 12.5 ...
Document Type: article in journal/newspaper
Language: English
DOI: 10.1093/ecco-jcc/jjad212.0896
Availability: https://doi.org/10.1093/ecco-jcc/jjad212.0896; https://academic.oup.com/ecco-jcc/article-pdf/18/Supplement_1/i1419/56349494/jjad212.0896.pdf
Rights: https://academic.oup.com/pages/standard-publication-reuse-rights
Accession Number: edsbas.F6800366
Database: BASE