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Japan College of Rheumatology 2009 guidelines for the use of tocilizumab, a humanized anti-interleukin-6 receptor monoclonal antibody, in rheumatoid arthritis
The introduction of biological agents targeting tumor necrosis factor-alpha (TNF-α) has brought about a paradigm shift in the treatment of rheumatoid arthritis (RA). Although these anti-TNF agents have excellent efficacy against RA, a substantial number of patients still show inadequate responses. I...
Autores principales: | , , , , , , , , , |
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Formato: | Texto |
Lenguaje: | English |
Publicado: |
Springer Japan
2009
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2720589/ https://www.ncbi.nlm.nih.gov/pubmed/19590933 http://dx.doi.org/10.1007/s10165-009-0197-6 |
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author | Koike, Ryuji Harigai, Masayoshi Atsumi, Tatsuya Amano, Koichi Kawai, Shinichi Saito, Kazuyoshi Saito, Tomoyuki Yamamura, Masahiro Matsubara, Tsukasa Miyasaka, Nobuyuki |
author_facet | Koike, Ryuji Harigai, Masayoshi Atsumi, Tatsuya Amano, Koichi Kawai, Shinichi Saito, Kazuyoshi Saito, Tomoyuki Yamamura, Masahiro Matsubara, Tsukasa Miyasaka, Nobuyuki |
author_sort | Koike, Ryuji |
collection | PubMed |
description | The introduction of biological agents targeting tumor necrosis factor-alpha (TNF-α) has brought about a paradigm shift in the treatment of rheumatoid arthritis (RA). Although these anti-TNF agents have excellent efficacy against RA, a substantial number of patients still show inadequate responses. In Western countries, such patients are already being treated with new classes of antirheumatic drugs such as abatacept and rituximab. Tocilizumab (TCZ) is a humanized monoclonal antibody developed in Japan against the human interleukin-6 (IL-6) receptor. TCZ does not only alleviate the signs and symptoms of RA but also seems to prevent progressive bone and joint destruction. However, there is a concern that TCZ might increase the risk of adverse events such as infections since IL-6 plays a pivotal role in the immune system. Calculating the relative risks of specific adverse outcomes with TCZ use remains difficult, due to insufficient patient numbers enrolled in clinical trials to date. This review presents tentative guidelines for the use of TCZ for RA patients prepared by the Japan College of Rheumatology and based on results of clinical trials in Japan and Western countries. The guidelines are intended as a guide for postmarketing surveillance and clinical practice, and will be revised periodically based on the surveillance. |
format | Text |
id | pubmed-2720589 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2009 |
publisher | Springer Japan |
record_format | MEDLINE/PubMed |
spelling | pubmed-27205892009-08-04 Japan College of Rheumatology 2009 guidelines for the use of tocilizumab, a humanized anti-interleukin-6 receptor monoclonal antibody, in rheumatoid arthritis Koike, Ryuji Harigai, Masayoshi Atsumi, Tatsuya Amano, Koichi Kawai, Shinichi Saito, Kazuyoshi Saito, Tomoyuki Yamamura, Masahiro Matsubara, Tsukasa Miyasaka, Nobuyuki Mod Rheumatol Review Article The introduction of biological agents targeting tumor necrosis factor-alpha (TNF-α) has brought about a paradigm shift in the treatment of rheumatoid arthritis (RA). Although these anti-TNF agents have excellent efficacy against RA, a substantial number of patients still show inadequate responses. In Western countries, such patients are already being treated with new classes of antirheumatic drugs such as abatacept and rituximab. Tocilizumab (TCZ) is a humanized monoclonal antibody developed in Japan against the human interleukin-6 (IL-6) receptor. TCZ does not only alleviate the signs and symptoms of RA but also seems to prevent progressive bone and joint destruction. However, there is a concern that TCZ might increase the risk of adverse events such as infections since IL-6 plays a pivotal role in the immune system. Calculating the relative risks of specific adverse outcomes with TCZ use remains difficult, due to insufficient patient numbers enrolled in clinical trials to date. This review presents tentative guidelines for the use of TCZ for RA patients prepared by the Japan College of Rheumatology and based on results of clinical trials in Japan and Western countries. The guidelines are intended as a guide for postmarketing surveillance and clinical practice, and will be revised periodically based on the surveillance. Springer Japan 2009-07-10 2009-08 /pmc/articles/PMC2720589/ /pubmed/19590933 http://dx.doi.org/10.1007/s10165-009-0197-6 Text en © Japan College of Rheumatology 2009 |
spellingShingle | Review Article Koike, Ryuji Harigai, Masayoshi Atsumi, Tatsuya Amano, Koichi Kawai, Shinichi Saito, Kazuyoshi Saito, Tomoyuki Yamamura, Masahiro Matsubara, Tsukasa Miyasaka, Nobuyuki Japan College of Rheumatology 2009 guidelines for the use of tocilizumab, a humanized anti-interleukin-6 receptor monoclonal antibody, in rheumatoid arthritis |
title | Japan College of Rheumatology 2009 guidelines for the use of tocilizumab, a humanized anti-interleukin-6 receptor monoclonal antibody, in rheumatoid arthritis |
title_full | Japan College of Rheumatology 2009 guidelines for the use of tocilizumab, a humanized anti-interleukin-6 receptor monoclonal antibody, in rheumatoid arthritis |
title_fullStr | Japan College of Rheumatology 2009 guidelines for the use of tocilizumab, a humanized anti-interleukin-6 receptor monoclonal antibody, in rheumatoid arthritis |
title_full_unstemmed | Japan College of Rheumatology 2009 guidelines for the use of tocilizumab, a humanized anti-interleukin-6 receptor monoclonal antibody, in rheumatoid arthritis |
title_short | Japan College of Rheumatology 2009 guidelines for the use of tocilizumab, a humanized anti-interleukin-6 receptor monoclonal antibody, in rheumatoid arthritis |
title_sort | japan college of rheumatology 2009 guidelines for the use of tocilizumab, a humanized anti-interleukin-6 receptor monoclonal antibody, in rheumatoid arthritis |
topic | Review Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2720589/ https://www.ncbi.nlm.nih.gov/pubmed/19590933 http://dx.doi.org/10.1007/s10165-009-0197-6 |
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