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Golimumab for the treatment of ulcerative colitis

Introduction: Tumor necrosis factor antagonists have revolutionized the therapeutic management of inflammatory bowel disease. Infliximab and adalimumab were the first biological agents used to induce and maintain remission in ulcerative colitis. More recently, a third tumor necrosis factor antagonis...

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Detalles Bibliográficos
Autores principales: Flamant, Mathurin, Paul, Stephane, Roblin, Xavier
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Taylor & Francis 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5490638/
https://www.ncbi.nlm.nih.gov/pubmed/28472597
http://dx.doi.org/10.1080/14712598.2017.1327576
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author Flamant, Mathurin
Paul, Stephane
Roblin, Xavier
author_facet Flamant, Mathurin
Paul, Stephane
Roblin, Xavier
author_sort Flamant, Mathurin
collection PubMed
description Introduction: Tumor necrosis factor antagonists have revolutionized the therapeutic management of inflammatory bowel disease. Infliximab and adalimumab were the first biological agents used to induce and maintain remission in ulcerative colitis. More recently, a third tumor necrosis factor antagonist, golimumab, was approved, extending the therapeutic approach for moderate-to-severe ulcerative colitis. Areas covered: In this review, the authors review the literature on the efficacy and safety of golimumab in the context of other anti-TNF agents used in the treatment of this disease. The role of therapeutic drug monitoring in the case of loss of response to an anti-TNF agent is also discussed. Expert opinion: Golimumab is currently effective to induce and maintain remission in patients with ulcerative colitis, especially those patients who are naive for an anti-TNF agent. No large studies have evaluated the efficacy of golimumab after failure of a first-line TNF antagonist therapy. In the case of loss of response to a first anti-TNF agent, therapeutic drug monitoring is essential to determine the most suitable therapeutic option.
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spelling pubmed-54906382017-07-11 Golimumab for the treatment of ulcerative colitis Flamant, Mathurin Paul, Stephane Roblin, Xavier Expert Opin Biol Ther Drug Evaluation Introduction: Tumor necrosis factor antagonists have revolutionized the therapeutic management of inflammatory bowel disease. Infliximab and adalimumab were the first biological agents used to induce and maintain remission in ulcerative colitis. More recently, a third tumor necrosis factor antagonist, golimumab, was approved, extending the therapeutic approach for moderate-to-severe ulcerative colitis. Areas covered: In this review, the authors review the literature on the efficacy and safety of golimumab in the context of other anti-TNF agents used in the treatment of this disease. The role of therapeutic drug monitoring in the case of loss of response to an anti-TNF agent is also discussed. Expert opinion: Golimumab is currently effective to induce and maintain remission in patients with ulcerative colitis, especially those patients who are naive for an anti-TNF agent. No large studies have evaluated the efficacy of golimumab after failure of a first-line TNF antagonist therapy. In the case of loss of response to a first anti-TNF agent, therapeutic drug monitoring is essential to determine the most suitable therapeutic option. Taylor & Francis 2017-07-03 2017-05-02 /pmc/articles/PMC5490638/ /pubmed/28472597 http://dx.doi.org/10.1080/14712598.2017.1327576 Text en © 2017 Informa UK Limited, trading as Taylor & Francis Group
spellingShingle Drug Evaluation
Flamant, Mathurin
Paul, Stephane
Roblin, Xavier
Golimumab for the treatment of ulcerative colitis
title Golimumab for the treatment of ulcerative colitis
title_full Golimumab for the treatment of ulcerative colitis
title_fullStr Golimumab for the treatment of ulcerative colitis
title_full_unstemmed Golimumab for the treatment of ulcerative colitis
title_short Golimumab for the treatment of ulcerative colitis
title_sort golimumab for the treatment of ulcerative colitis
topic Drug Evaluation
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5490638/
https://www.ncbi.nlm.nih.gov/pubmed/28472597
http://dx.doi.org/10.1080/14712598.2017.1327576
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