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Tocilizumab is effective against polymyalgia rheumatica: experience in 13 intractable cases
Polymyalgia rheumatica (PMR) affects older people, and although glucocorticoids are effective in treating PMR, they frequently result in side effects. Therefore, we conducted a retrospective study to assess the effectiveness and safety of tocilizumab as an alternative to glucocorticoids. We included...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BMJ Publishing Group
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4663453/ https://www.ncbi.nlm.nih.gov/pubmed/26635968 http://dx.doi.org/10.1136/rmdopen-2015-000162 |
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author | Izumi, Keisuke Kuda, Harumi Ushikubo, Mari Kuwana, Masataka Takeuchi, Tsutomu Oshima, Hisaji |
author_facet | Izumi, Keisuke Kuda, Harumi Ushikubo, Mari Kuwana, Masataka Takeuchi, Tsutomu Oshima, Hisaji |
author_sort | Izumi, Keisuke |
collection | PubMed |
description | Polymyalgia rheumatica (PMR) affects older people, and although glucocorticoids are effective in treating PMR, they frequently result in side effects. Therefore, we conducted a retrospective study to assess the effectiveness and safety of tocilizumab as an alternative to glucocorticoids. We included 13 consecutive patients with PMR (11 women and 2 men; median age, 74 years) diagnosed according to Bird's criteria and the 2012 European League Against Rheumatism/American College of Rheumatology provisional classification criteria. All patients received tocilizumab infusion (8 mg/kg every 4 weeks) at our institutions, between 2008 and 2014, because of PMR relapses (n=12) or insufficient response to initial prednisolone treatment (n=1), without increasing prednisolone dosage. Seven patients were on methotrexate, and all had one or more glucocorticoid-related comorbidities. Administration of tocilizumab significantly improved inflammation and PMR symptoms such as morning stiffness, as well as the Patient-Pain and Patient-Global Assessment visual analogue scales (p<0.05). Proximal muscle pain disappeared within 8 weeks, on average, and the Health Assessment Questionnaire-Disability Index scores (p=0.098) and concomitant prednisolone doses (p<0.05) decreased at 12 weeks. Severe adverse events were not observed during the mean tocilizumab treatment period of 43.4 weeks. Our findings suggest that tocilizumab is effective and safe for PMR treatment. |
format | Online Article Text |
id | pubmed-4663453 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | BMJ Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-46634532015-12-03 Tocilizumab is effective against polymyalgia rheumatica: experience in 13 intractable cases Izumi, Keisuke Kuda, Harumi Ushikubo, Mari Kuwana, Masataka Takeuchi, Tsutomu Oshima, Hisaji RMD Open Vasculitis Polymyalgia rheumatica (PMR) affects older people, and although glucocorticoids are effective in treating PMR, they frequently result in side effects. Therefore, we conducted a retrospective study to assess the effectiveness and safety of tocilizumab as an alternative to glucocorticoids. We included 13 consecutive patients with PMR (11 women and 2 men; median age, 74 years) diagnosed according to Bird's criteria and the 2012 European League Against Rheumatism/American College of Rheumatology provisional classification criteria. All patients received tocilizumab infusion (8 mg/kg every 4 weeks) at our institutions, between 2008 and 2014, because of PMR relapses (n=12) or insufficient response to initial prednisolone treatment (n=1), without increasing prednisolone dosage. Seven patients were on methotrexate, and all had one or more glucocorticoid-related comorbidities. Administration of tocilizumab significantly improved inflammation and PMR symptoms such as morning stiffness, as well as the Patient-Pain and Patient-Global Assessment visual analogue scales (p<0.05). Proximal muscle pain disappeared within 8 weeks, on average, and the Health Assessment Questionnaire-Disability Index scores (p=0.098) and concomitant prednisolone doses (p<0.05) decreased at 12 weeks. Severe adverse events were not observed during the mean tocilizumab treatment period of 43.4 weeks. Our findings suggest that tocilizumab is effective and safe for PMR treatment. BMJ Publishing Group 2015-11-27 /pmc/articles/PMC4663453/ /pubmed/26635968 http://dx.doi.org/10.1136/rmdopen-2015-000162 Text en Published by the BMJ Publishing Group Limited. For permission to use (where not already granted under a licence) please go to http://www.bmj.com/company/products-services/rights-and-licensing/ This is an Open Access article distributed in accordance with the Creative Commons Attribution Non Commercial (CC BY-NC 4.0) license, which permits others to distribute, remix, adapt, build upon this work non-commercially, and license their derivative works on different terms, provided the original work is properly cited and the use is non-commercial. See: http://creativecommons.org/licenses/by-nc/4.0/ |
spellingShingle | Vasculitis Izumi, Keisuke Kuda, Harumi Ushikubo, Mari Kuwana, Masataka Takeuchi, Tsutomu Oshima, Hisaji Tocilizumab is effective against polymyalgia rheumatica: experience in 13 intractable cases |
title | Tocilizumab is effective against polymyalgia rheumatica: experience in 13 intractable cases |
title_full | Tocilizumab is effective against polymyalgia rheumatica: experience in 13 intractable cases |
title_fullStr | Tocilizumab is effective against polymyalgia rheumatica: experience in 13 intractable cases |
title_full_unstemmed | Tocilizumab is effective against polymyalgia rheumatica: experience in 13 intractable cases |
title_short | Tocilizumab is effective against polymyalgia rheumatica: experience in 13 intractable cases |
title_sort | tocilizumab is effective against polymyalgia rheumatica: experience in 13 intractable cases |
topic | Vasculitis |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4663453/ https://www.ncbi.nlm.nih.gov/pubmed/26635968 http://dx.doi.org/10.1136/rmdopen-2015-000162 |
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