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Budesonide Orodispersible Tablets Maintain Remission in a Randomized, Placebo-Controlled Trial of Patients With Eosinophilic Esophagitis.

Straumann, A; Lucendo, AJ; Miehlke, S; Vieth, M; Schlag, C; Biedermann, L; Vaquero, CS; Ciriza de Los Rios, C; Schmoecker, C; Madisch, A; et al. Straumann, A; Lucendo, AJ; Miehlke, S; Vieth, M; Schlag, C; Biedermann, L; Vaquero, CS; Ciriza de Los Rios, C; Schmoecker, C; Madisch, A; Hruz, P; Hayat, J; von Arnim, U; Bredenoord, AJ; Schubert, S; Mueller, R; Greinwald, R; Schoepfer, A; Attwood, S; International EOS-2 Study Group (2020) Budesonide Orodispersible Tablets Maintain Remission in a Randomized, Placebo-Controlled Trial of Patients With Eosinophilic Esophagitis. Gastroenterology, 159 (5). 1672-1685.e5. ISSN 1528-0012 https://doi.org/10.1053/j.gastro.2020.07.039
SGUL Authors: Hayat, Jamal

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Abstract

BACKGROUND & AIMS: Eosinophilic esophagitis (EoE) is a chronic inflammatory disorder. Swallowed topical-acting corticosteroids are effective in bringing active EoE into remission. However, it is not clear whether these drugs are effective for long-term maintenance of remission. METHODS: We performed a double-blind trial to compare the efficacy and safety of 2 dosages of a budesonide orodispersible tablet (BOT) vs placebo in maintaining remission of EoE. Maintenance of remission was defined as absence of clinical and histologic relapse and no premature withdrawal for any reason. Two hundred and four adults with EoE in clinical and histologic remission, from 29 European study sites, were randomly assigned to groups given BOT 0.5 mg twice daily (n = 68), BOT 1.0 mg twice daily (n = 68), or placebo twice daily (n = 68) for up to 48 weeks. RESULTS: At end of treatment, 73.5% of patients receiving BOT 0.5 mg twice daily and 75% receiving BOT 1.0 mg twice daily were in persistent remission compared with 4.4% of patients in the placebo group (P < .001 for both comparisons of BOT with placebo). Median time to relapse in the placebo group was 87 days. The frequency of adverse events was similar in the BOT and placebo groups. Morning serum levels of cortisol were in the normal range at baseline and did not significantly change during treatment. Four patients receiving BOT developed asymptomatic, low serum levels of cortisol. Clinically manifested candidiasis was suspected in 16.2% of patients in the BOT 0.5 mg group and in 11.8% of patients in the BOT 1.0 mg group; all infections resolved with treatment. CONCLUSIONS: In a phase 3 trial, up to 48 weeks of treatment with BOT (0.5 mg or 1.0 mg twice daily) was superior to placebo in maintaining remission of EoE. Both dosages were equally effective and well tolerated. EudraCT number; 2014-001485-99; ClinicalTrials.gov number, NCT02434029.

Item Type: Article
Additional Information: © 2020 by the AGA Institute. Published by Elsevier Inc. This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
Keywords: Dysphagia, Patient-Reported Outcomes, Remission, Topical Corticosteroids, Administration, Oral, Adrenal Cortex Hormones, Adult, Budesonide, Double-Blind Method, Eosinophilic Esophagitis, Europe, Female, Humans, Male, Middle Aged, Remission Induction, Tablets, Time Factors, Treatment Outcome, International EOS-2 Study Group, Humans, Budesonide, Adrenal Cortex Hormones, Tablets, Treatment Outcome, Remission Induction, Administration, Oral, Double-Blind Method, Time Factors, Adult, Middle Aged, Europe, Female, Male, Eosinophilic Esophagitis, Topical Corticosteroids, Dysphagia, Remission, Patient-Reported Outcomes, 1103 Clinical Sciences, 1114 Paediatrics and Reproductive Medicine, 1109 Neurosciences, Gastroenterology & Hepatology
SGUL Research Institute / Research Centre: Academic Structure > Institute of Medical & Biomedical Education (IMBE)
Journal or Publication Title: Gastroenterology
ISSN: 1528-0012
Language: eng
Dates:
DateEvent
November 2020Published
25 July 2020Published Online
21 July 2020Accepted
Publisher License: Creative Commons: Attribution-Noncommercial-No Derivative Works 4.0
PubMed ID: 32721437
Web of Science ID: WOS:000591420700012
Go to PubMed abstract
URI: https://openaccess.sgul.ac.uk/id/eprint/114124
Publisher's version: https://doi.org/10.1053/j.gastro.2020.07.039

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