Literature DB >> 27899263

Adalimumab dose escalation is effective and well tolerated in Crohn's disease patients with secondary loss of response to adalimumab.

Nicolas Duveau1, Maria Nachury1, Romain Gerard1, Julien Branche1, Vincent Maunoury1, Medina Boualit1, Pauline Wils1, Pierre Desreumaux1, Benjamin Pariente2.   

Abstract

BACKGROUND: Although adalimumab is effective in Crohn's disease, most patients experience a loss of response over time. The aim of the present study was to evaluate efficacy and safety of adalimumab dose escalation and identify predictors of a clinical response in Crohn's disease patients with a secondary loss of response.
METHODS: We performed a retrospective and observational study including all Crohn's disease patients who underwent dose escalation of adalimumab after a secondary loss of response from 2007 to 2015.
RESULTS: A clinical response was observed in 99/124 (79%) patients at 3 months and in 62/107 (61%) patients at 12 months. The predictive factors of response to ADA dose escalation at 12 months on multivariate analysis were: maintenance therapy of 40mg every week rather than 80mg every other week (OR 3.64, 95% CI: 1.28-10.37) and a CRP level≤5mg/L at adalimumab dose escalation (OR 6.64, 95% CI: 1.40-27.53). Adalimumab was withdrawn in 4 patients due to side effects.
CONCLUSIONS: Adalimumab dose escalation is an effective and well-tolerated therapeutic option in patients with secondary loss of response. A 40mg every week optimized regimen was predictive of a response to ADA dose escalation.
Copyright © 2016 Editrice Gastroenterologica Italiana S.r.l. Published by Elsevier Ltd. All rights reserved.

Entities:  

Keywords:  Anti-TNF; Optimization; Therapeutic strategy

Mesh:

Substances:

Year:  2016        PMID: 27899263     DOI: 10.1016/j.dld.2016.11.002

Source DB:  PubMed          Journal:  Dig Liver Dis        ISSN: 1590-8658            Impact factor:   4.088


  6 in total

1.  Subtherapeutic concentrations of infliximab and adalimumab are associated with increased disease activity in Crohn's disease.

Authors:  Arne Carlsen; Roald Omdal; Kristian Øgreid Leitao; Kjetil Isaksen; Anne Kristine Hetta; Lars Normann Karlsen; Lars Aabakken; Nils Bolstad; David Warren; Knut E A Lundin; Tore Grimstad
Journal:  Therap Adv Gastroenterol       Date:  2018-03-14       Impact factor: 4.409

2.  Adalimumab Dose-Escalation Therapy Is Effective in Refractory Crohn's Disease Patients with Loss of Response to Adalimumab, Especially in Cases without Previous Infliximab Treatment.

Authors:  Taketo Suzuki; Tsutomu Mizoshita; Tomoya Sugiyama; Yoshikazu Hirata; Yoshihide Kimura; Yuka Suzuki; Tomonori Yamada; Hironobu Tsukamoto; Takashi Mizushima; Naomi Sugimura; Takahito Katano; Satoshi Tanida; Hiromi Kataoka; Makoto Sasaki
Journal:  Case Rep Gastroenterol       Date:  2019-02-06

3.  Optimizing biologic therapy in inflammatory bowel disease: a Delphi consensus in the United Arab Emirates.

Authors:  Vito Annese; Rahul Nathwani; Maryam Alkhatry; Ahmad Al-Rifai; Sameer Al Awadhi; Filippos Georgopoulos; Ahmad N Jazzar; Ahmed M Khassouan; Zaher Koutoubi; Mazen S Taha; Jimmy K Limdi
Journal:  Therap Adv Gastroenterol       Date:  2021-12-22       Impact factor: 4.409

4.  Systematic review and meta-analysis: evaluating response to empiric anti-TNF dose intensification for secondary loss of response in Crohn's disease.

Authors:  Ashish Srinivasan; Robert Gilmore; Daniel van Langenberg; Peter De Cruz
Journal:  Therap Adv Gastroenterol       Date:  2022-02-02       Impact factor: 4.409

Review 5.  Introducing Patterns of Variability for Overcoming Compensatory Adaptation of the Immune System to Immunomodulatory Agents: A Novel Method for Improving Clinical Response to Anti-TNF Therapies.

Authors:  Tawfik Khoury; Yaron Ilan
Journal:  Front Immunol       Date:  2019-11-20       Impact factor: 7.561

Review 6.  Frequency and Effectiveness of Empirical Anti-TNF Dose Intensification in Inflammatory Bowel Disease: Systematic Review with Meta-Analysis.

Authors:  Laura Guberna; Olga P Nyssen; María Chaparro; Javier P Gisbert
Journal:  J Clin Med       Date:  2021-05-14       Impact factor: 4.241

  6 in total

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