Literature DB >> 25066841

Withdrawal of immunomodulators after co-treatment does not reduce trough level of infliximab in patients with Crohn's disease.

David Drobne1, Peter Bossuyt1, Christine Breynaert1, Tom Cattaert1, Niels Vande Casteele1, Griet Compernolle1, Matthias Jürgens1, Marc Ferrante1, Vera Ballet1, Willem-Jan Wollants1, Isabelle Cleynen1, Kristel Van Steen1, Ann Gils1, Paul Rutgeerts1, Severine Vermeire1, Gert Van Assche2.   

Abstract

BACKGROUND & AIMS: The addition of immunomodulators increases the efficacy of maintenance therapy with infliximab for up to 1 year in patients with Crohn's disease who have not been previously treated with immunomodulators. However, there are questions about the effect of withdrawing immunomodulator therapy from these patients. We studied the effects of treatment with infliximab and immunomodulators (co-treatment) and then immunomodulator withdrawal on long-term outcomes of patients, as well as trough levels of infliximab and formation of anti-infliximab antibodies (ATI).
METHODS: In a retrospective study with the median follow-up period of 34 months (interquartile range, 19-58 months), we analyzed data from 223 patients treated for Crohn's disease between May 1999 and December 2010 at the University Hospitals, Leuven, Belgium (65 received infliximab monotherapy, 158 received infliximab and an immunomodulator). Trough levels of infliximab and levels of ATI were measured in blood samples collected from 117 patients throughout co-treatment, as well as the time of immunomodulator withdrawal and after withdrawal.
RESULTS: Patients receiving co-treatment had higher trough levels of infliximab (adjusted mean increase, 1.44-fold) than those receiving infliximab monotherapy (95% confidence interval [CI], 1.07-1.92; P = .02). A smaller percentage of patients receiving co-treatment developed ATI (35 of 158, 22%) than those receiving infliximab monotherapy (25 of 65, 38%; P = .01). Among co-treated patients, levels of infliximab remained stable after immunomodulators were withdrawn (before: 3.2 μg/mL; 95% CI, 1.6-5.8 μg/mL and after: 3.7 μg/mL; 95% CI, 1.3-6.3 μg/mL; P = .70). After withdrawal of immunomodulators, 45 of 117 patients (38%) required increasing doses of infliximab, and 21 of 117 (18%) discontinued infliximab. At the time of immunomodulator withdrawal, trough levels of infliximab and C-reactive protein were most strongly associated with response to infliximab thereafter.
CONCLUSIONS: In a retrospective analysis, we confirmed that withdrawal of immunomodulators after at least 6 months (median, 13 months) of co-treatment with infliximab does not reduce the trough levels of infliximab in patients with Crohn's disease. Detectable trough levels of infliximab at the time of immunomodulator withdrawal are associated with long-term response.
Copyright © 2015 AGA Institute. Published by Elsevier Inc. All rights reserved.

Entities:  

Keywords:  Azathioprine; Inflammatory Bowel Disease; Methotrexate; Pharmacokinetic

Mesh:

Substances:

Year:  2014        PMID: 25066841     DOI: 10.1016/j.cgh.2014.07.027

Source DB:  PubMed          Journal:  Clin Gastroenterol Hepatol        ISSN: 1542-3565            Impact factor:   11.382


  33 in total

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Review 3.  Therapeutic Drug Monitoring in Pediatric Inflammatory Bowel Disease.

Authors:  Nicholas Carman; David R Mack; Eric I Benchimol
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Review 4.  Therapy for Crohn's Disease: a Review of Recent Developments.

Authors:  Gregory J Eustace; Gil Y Melmed
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Review 5.  Optimizing Biologic Agents in Ulcerative Colitis and Crohn's Disease.

Authors:  Aoibhlinn O'Toole; Alan C Moss
Journal:  Curr Gastroenterol Rep       Date:  2015-08

Review 6.  De-escalation of Therapy in Inflammatory Bowel Disease.

Authors:  Catarina Frias Gomes; Jean-Frédéric Colombel; Joana Torres
Journal:  Curr Gastroenterol Rep       Date:  2018-07-02

7.  Infliximab Maintenance Dosing in Inflammatory Bowel Disease: an Example for In Silico Assessment of Adaptive Dosing Strategies.

Authors:  Jessica Wojciechowski; Richard N Upton; Diane R Mould; Michael D Wiese; David J R Foster
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8.  Appropriate Therapeutic Drug Monitoring of Biologic Agents for Patients With Inflammatory Bowel Diseases.

Authors:  Konstantinos Papamichael; Adam S Cheifetz; Gil Y Melmed; Peter M Irving; Niels Vande Casteele; Patricia L Kozuch; Laura E Raffals; Leonard Baidoo; Brian Bressler; Shane M Devlin; Jennifer Jones; Gilaad G Kaplan; Miles P Sparrow; Fernando S Velayos; Thomas Ullman; Corey A Siegel
Journal:  Clin Gastroenterol Hepatol       Date:  2019-03-27       Impact factor: 11.382

9.  Improved Population Pharmacokinetic Model for Predicting Optimized Infliximab Exposure in Pediatric Inflammatory Bowel Disease.

Authors:  Laura E Bauman; Ye Xiong; Tomoyuki Mizuno; Philip Minar; Tsuyoshi Fukuda; Min Dong; Michael J Rosen; Alexander A Vinks
Journal:  Inflamm Bowel Dis       Date:  2020-02-11       Impact factor: 5.325

Review 10.  Practical Approaches to "Top-Down" Therapies for Crohn's Disease.

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Journal:  Curr Gastroenterol Rep       Date:  2016-07
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