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An indirect comparison of infliximab versus adalimumab or golimumab for active ulcerative colitis

INTRODUCTION: The aim of the study was to compare adalimumab or golimumab with infliximab in patients with moderately-to-severely active ulcerative colitis (UC). MATERIAL AND METHODS: This paper was prepared according to the PRISMA guidelines. The systematic literature search was performed in PubMed...

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Autores principales: Kawalec, Paweł, Pilc, Andrzej
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Termedia Publishing House 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5016577/
https://www.ncbi.nlm.nih.gov/pubmed/27695502
http://dx.doi.org/10.5114/aoms.2016.58682
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author Kawalec, Paweł
Pilc, Andrzej
author_facet Kawalec, Paweł
Pilc, Andrzej
author_sort Kawalec, Paweł
collection PubMed
description INTRODUCTION: The aim of the study was to compare adalimumab or golimumab with infliximab in patients with moderately-to-severely active ulcerative colitis (UC). MATERIAL AND METHODS: This paper was prepared according to the PRISMA guidelines. The systematic literature search was performed in PubMed, Embase, and Cochrane Library. No direct head-to-head comparisons for infliximab vs. adalimumab or golimumab were available so an indirect comparison according to the Bucher method was performed after a homogeneity evaluation of the included studies. RESULTS: Six RCTs were included in the systematic review. An indirect comparison was performed, which revealed that infliximab was more effective in inducing clinical response compared with both doses of adalimumab (160/80 mg or 80/40 mg; p < 0.05), and, in clinical remission, infliximab was more effective than adalimumab (only for a dosage regime of 80/40 mg; p < 0.05). No statistically significant differences in clinical response and clinical remission were observed between infliximab and golimumab in the induction phase. A significant (p < 0.05) advantage only of infliximab compared with adalimumab at doses of 80/40 mg and 80/160 mg was seen in terms of clinical response in the maintenance phase (up to 52–54 weeks). The indirect comparison revealed that serious adverse events were significantly more frequent among patients treated with a maintenance dose of 100 mg of golimumab compared with those treated with infliximab (p < 0.05). CONCLUSIONS: No significant differences in efficacy in the maintenance phase between infliximab and golimumab or adalimumab were revealed. Infliximab proved to be more effective than adalimumab but of similar efficacy to that of golimumab in the induction phase.
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spelling pubmed-50165772016-10-01 An indirect comparison of infliximab versus adalimumab or golimumab for active ulcerative colitis Kawalec, Paweł Pilc, Andrzej Arch Med Sci Systematic review/Meta-analysis INTRODUCTION: The aim of the study was to compare adalimumab or golimumab with infliximab in patients with moderately-to-severely active ulcerative colitis (UC). MATERIAL AND METHODS: This paper was prepared according to the PRISMA guidelines. The systematic literature search was performed in PubMed, Embase, and Cochrane Library. No direct head-to-head comparisons for infliximab vs. adalimumab or golimumab were available so an indirect comparison according to the Bucher method was performed after a homogeneity evaluation of the included studies. RESULTS: Six RCTs were included in the systematic review. An indirect comparison was performed, which revealed that infliximab was more effective in inducing clinical response compared with both doses of adalimumab (160/80 mg or 80/40 mg; p < 0.05), and, in clinical remission, infliximab was more effective than adalimumab (only for a dosage regime of 80/40 mg; p < 0.05). No statistically significant differences in clinical response and clinical remission were observed between infliximab and golimumab in the induction phase. A significant (p < 0.05) advantage only of infliximab compared with adalimumab at doses of 80/40 mg and 80/160 mg was seen in terms of clinical response in the maintenance phase (up to 52–54 weeks). The indirect comparison revealed that serious adverse events were significantly more frequent among patients treated with a maintenance dose of 100 mg of golimumab compared with those treated with infliximab (p < 0.05). CONCLUSIONS: No significant differences in efficacy in the maintenance phase between infliximab and golimumab or adalimumab were revealed. Infliximab proved to be more effective than adalimumab but of similar efficacy to that of golimumab in the induction phase. Termedia Publishing House 2016-03-22 2016-10-01 /pmc/articles/PMC5016577/ /pubmed/27695502 http://dx.doi.org/10.5114/aoms.2016.58682 Text en Copyright: © 2016 Termedia & Banach http://creativecommons.org/licenses/by-nc-sa/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International (CC BY-NC-SA 4.0) License, allowing third parties to copy and redistribute the material in any medium or format and to remix, transform, and build upon the material, provided the original work is properly cited and states its license.
spellingShingle Systematic review/Meta-analysis
Kawalec, Paweł
Pilc, Andrzej
An indirect comparison of infliximab versus adalimumab or golimumab for active ulcerative colitis
title An indirect comparison of infliximab versus adalimumab or golimumab for active ulcerative colitis
title_full An indirect comparison of infliximab versus adalimumab or golimumab for active ulcerative colitis
title_fullStr An indirect comparison of infliximab versus adalimumab or golimumab for active ulcerative colitis
title_full_unstemmed An indirect comparison of infliximab versus adalimumab or golimumab for active ulcerative colitis
title_short An indirect comparison of infliximab versus adalimumab or golimumab for active ulcerative colitis
title_sort indirect comparison of infliximab versus adalimumab or golimumab for active ulcerative colitis
topic Systematic review/Meta-analysis
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5016577/
https://www.ncbi.nlm.nih.gov/pubmed/27695502
http://dx.doi.org/10.5114/aoms.2016.58682
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