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Tocilizumab in Large Vessel Vasculitis – Different Routes of Administration

BACKGROUND: Tocilizumab is increasingly used in the treatment of large vessel vasculitis with recent approval for giant cell arteritis. OBJECTIVE: To determine the efficacy and safety of tocilizumab in large vessel vasculitis in a real-life setting using different routes of administration. METHODS:...

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Autores principales: Schmalzing, Marc, Gadeholt, Ottar, Gernert, Michael, Tony, Hans-Peter, Schwaneck, Eva C
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Bentham Open 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6128017/
https://www.ncbi.nlm.nih.gov/pubmed/30258504
http://dx.doi.org/10.2174/1874312901812010152
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author Schmalzing, Marc
Gadeholt, Ottar
Gernert, Michael
Tony, Hans-Peter
Schwaneck, Eva C
author_facet Schmalzing, Marc
Gadeholt, Ottar
Gernert, Michael
Tony, Hans-Peter
Schwaneck, Eva C
author_sort Schmalzing, Marc
collection PubMed
description BACKGROUND: Tocilizumab is increasingly used in the treatment of large vessel vasculitis with recent approval for giant cell arteritis. OBJECTIVE: To determine the efficacy and safety of tocilizumab in large vessel vasculitis in a real-life setting using different routes of administration. METHODS: Retrospective analysis of consecutive patients at a tertiary rheumatology department who received tocilizumab for large vessel vasculitis. RESULTS: A total of 11 patients were treated with tocilizumab (8 giant cell arteritis, 2 large vessel vasculitis associated with rheumatoid arthritis, 1 Takayasu arteritis) after a median of 2 other steroid-sparing agents (range 1-4). Of these, 9 received tocilizumab as salvage therapy for active vasculitis and 2 due to the toxicity of their former steroid-sparing medication. After a mean follow-up of 23 months 7 patients were in remission as to vasculitis under a mean prednisolone dose of 1.7 ± 1.5 mg; one patient relapsed after long term remission having discontinued tocilizumab for elective surgery; one patient stopped tocilizumab after attributable infectious complications, and two patients died: one due to complications of vascular surgery, probably not attributable to tocilizumab; and the other due to sepsis secondary to sigmoiditis. Only 3 relapses occurred under continuous tocilizumab treatment. In all these 3 cases, renewed remission could be achieved by switching from subcutaneous (162 mg qw) to intravenous tocilizumab (8mg/kg q4w). CONCLUSION: Tocilizumab is efficacious in patients with large vessel vasculitis in a real-life situation. Safety appears to be acceptable, but infectious complications have to be considered. Intravenous tocilizumab may be used in patients who relapse under subcutaneous application.
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spelling pubmed-61280172018-09-26 Tocilizumab in Large Vessel Vasculitis – Different Routes of Administration Schmalzing, Marc Gadeholt, Ottar Gernert, Michael Tony, Hans-Peter Schwaneck, Eva C Open Rheumatol J Rheumatology BACKGROUND: Tocilizumab is increasingly used in the treatment of large vessel vasculitis with recent approval for giant cell arteritis. OBJECTIVE: To determine the efficacy and safety of tocilizumab in large vessel vasculitis in a real-life setting using different routes of administration. METHODS: Retrospective analysis of consecutive patients at a tertiary rheumatology department who received tocilizumab for large vessel vasculitis. RESULTS: A total of 11 patients were treated with tocilizumab (8 giant cell arteritis, 2 large vessel vasculitis associated with rheumatoid arthritis, 1 Takayasu arteritis) after a median of 2 other steroid-sparing agents (range 1-4). Of these, 9 received tocilizumab as salvage therapy for active vasculitis and 2 due to the toxicity of their former steroid-sparing medication. After a mean follow-up of 23 months 7 patients were in remission as to vasculitis under a mean prednisolone dose of 1.7 ± 1.5 mg; one patient relapsed after long term remission having discontinued tocilizumab for elective surgery; one patient stopped tocilizumab after attributable infectious complications, and two patients died: one due to complications of vascular surgery, probably not attributable to tocilizumab; and the other due to sepsis secondary to sigmoiditis. Only 3 relapses occurred under continuous tocilizumab treatment. In all these 3 cases, renewed remission could be achieved by switching from subcutaneous (162 mg qw) to intravenous tocilizumab (8mg/kg q4w). CONCLUSION: Tocilizumab is efficacious in patients with large vessel vasculitis in a real-life situation. Safety appears to be acceptable, but infectious complications have to be considered. Intravenous tocilizumab may be used in patients who relapse under subcutaneous application. Bentham Open 2018-08-31 /pmc/articles/PMC6128017/ /pubmed/30258504 http://dx.doi.org/10.2174/1874312901812010152 Text en © 2018 Schmalzing et al. https://creativecommons.org/licenses/by/4.0/legalcode This is an open access article distributed under the terms of the Creative Commons Attribution 4.0 International Public License (CC-BY 4.0), a copy of which is available at: (https://creativecommons.org/licenses/by/4.0/legalcode). This license permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Rheumatology
Schmalzing, Marc
Gadeholt, Ottar
Gernert, Michael
Tony, Hans-Peter
Schwaneck, Eva C
Tocilizumab in Large Vessel Vasculitis – Different Routes of Administration
title Tocilizumab in Large Vessel Vasculitis – Different Routes of Administration
title_full Tocilizumab in Large Vessel Vasculitis – Different Routes of Administration
title_fullStr Tocilizumab in Large Vessel Vasculitis – Different Routes of Administration
title_full_unstemmed Tocilizumab in Large Vessel Vasculitis – Different Routes of Administration
title_short Tocilizumab in Large Vessel Vasculitis – Different Routes of Administration
title_sort tocilizumab in large vessel vasculitis – different routes of administration
topic Rheumatology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6128017/
https://www.ncbi.nlm.nih.gov/pubmed/30258504
http://dx.doi.org/10.2174/1874312901812010152
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