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Early intervention in the treatment of rheumatoid arthritis: focus on tocilizumab

Tocilizumab is a fully humanized monoclonal antibody against interleukin-6 receptors that was approved for the treatment of patients with rheumatoid arthritis (RA). Several lines of evidence, obtained both from conventional disease-modifying anti-rheumatic drugs (DMARDs) and tumor necrosis factor (T...

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Detalles Bibliográficos
Autores principales: Yilmaz, Sedat, Simsek, Ismail
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Dove Medical Press 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3810895/
https://www.ncbi.nlm.nih.gov/pubmed/24179334
http://dx.doi.org/10.2147/TCRM.S35784
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author Yilmaz, Sedat
Simsek, Ismail
author_facet Yilmaz, Sedat
Simsek, Ismail
author_sort Yilmaz, Sedat
collection PubMed
description Tocilizumab is a fully humanized monoclonal antibody against interleukin-6 receptors that was approved for the treatment of patients with rheumatoid arthritis (RA). Several lines of evidence, obtained both from conventional disease-modifying anti-rheumatic drugs (DMARDs) and tumor necrosis factor (TNF) inhibitors, have supported the concept of “window of opportunity” as showing that these therapies consistently work better in early disease as compared to established RA. This review addresses the question of whether a window of opportunity gained with conventional DMARDs and TNF inhibitors can also be achieved with tocilizumab. To this end, data regarding the use of tocilizumab in early RA patients are summarized. Currently available data suggest that the earlier the treatment with tocilizumab, the better the clinical outcome can be, which may have implications for various aspects of RA treatment strategies.
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spelling pubmed-38108952013-10-31 Early intervention in the treatment of rheumatoid arthritis: focus on tocilizumab Yilmaz, Sedat Simsek, Ismail Ther Clin Risk Manag Review Tocilizumab is a fully humanized monoclonal antibody against interleukin-6 receptors that was approved for the treatment of patients with rheumatoid arthritis (RA). Several lines of evidence, obtained both from conventional disease-modifying anti-rheumatic drugs (DMARDs) and tumor necrosis factor (TNF) inhibitors, have supported the concept of “window of opportunity” as showing that these therapies consistently work better in early disease as compared to established RA. This review addresses the question of whether a window of opportunity gained with conventional DMARDs and TNF inhibitors can also be achieved with tocilizumab. To this end, data regarding the use of tocilizumab in early RA patients are summarized. Currently available data suggest that the earlier the treatment with tocilizumab, the better the clinical outcome can be, which may have implications for various aspects of RA treatment strategies. Dove Medical Press 2013 2013-10-25 /pmc/articles/PMC3810895/ /pubmed/24179334 http://dx.doi.org/10.2147/TCRM.S35784 Text en © 2013 Yilmaz and Simsek. This work is published by Dove Medical Press Limited, and licensed under Creative Commons Attribution – Non Commercial (unported, v3.0) License The full terms of the License are available at http://creativecommons.org/licenses/by-nc/3.0/. Non-commercial uses of the work are permitted without any further permission from Dove Medical Press Limited, provided the work is properly attributed.
spellingShingle Review
Yilmaz, Sedat
Simsek, Ismail
Early intervention in the treatment of rheumatoid arthritis: focus on tocilizumab
title Early intervention in the treatment of rheumatoid arthritis: focus on tocilizumab
title_full Early intervention in the treatment of rheumatoid arthritis: focus on tocilizumab
title_fullStr Early intervention in the treatment of rheumatoid arthritis: focus on tocilizumab
title_full_unstemmed Early intervention in the treatment of rheumatoid arthritis: focus on tocilizumab
title_short Early intervention in the treatment of rheumatoid arthritis: focus on tocilizumab
title_sort early intervention in the treatment of rheumatoid arthritis: focus on tocilizumab
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3810895/
https://www.ncbi.nlm.nih.gov/pubmed/24179334
http://dx.doi.org/10.2147/TCRM.S35784
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