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IL-6 blockade in systemic juvenile idiopathic arthritis – achievement of inactive disease and remission (data from the German AID-registry)
BACKGROUND: Systemic juvenile idiopathic arthritis (sJIA) is a complex disease with an autoinflammatory component of unknown etiology related to the innate immune system. A major role in the pathogenesis has been ascribed to proinflammatory cytokines like interleukin-6 (IL-6), and effective drugs in...
Autores principales: | , , , , , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5887199/ https://www.ncbi.nlm.nih.gov/pubmed/29622022 http://dx.doi.org/10.1186/s12969-018-0236-y |
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author | Bielak, M. Husmann, E. Weyandt, N. Haas, J.-P. Hügle, B. Horneff, G. Neudorf, U. Lutz, T. Lilienthal, E. Kallinich, T. Tenbrock, K. Berendes, R. Niehues, T. Wittkowski, H. Weißbarth-Riedel, E. Heubner, G. Oommen, P. Klotsche, J. Foell, Dirk Lainka, E. |
author_facet | Bielak, M. Husmann, E. Weyandt, N. Haas, J.-P. Hügle, B. Horneff, G. Neudorf, U. Lutz, T. Lilienthal, E. Kallinich, T. Tenbrock, K. Berendes, R. Niehues, T. Wittkowski, H. Weißbarth-Riedel, E. Heubner, G. Oommen, P. Klotsche, J. Foell, Dirk Lainka, E. |
author_sort | Bielak, M. |
collection | PubMed |
description | BACKGROUND: Systemic juvenile idiopathic arthritis (sJIA) is a complex disease with an autoinflammatory component of unknown etiology related to the innate immune system. A major role in the pathogenesis has been ascribed to proinflammatory cytokines like interleukin-6 (IL-6), and effective drugs inhibiting their signaling are being developed. This study evaluates sJIA patients treated with the IL-6 inhibitor tocilizumab (TCZ) concerning clinical response rate, disease course and adverse effects in a real-life clinical setting. METHODS: In 2009 a clinical and research consortium was established, including an online registry for autoinflammatory diseases (AID) (https://aid-register.de). Data for this retrospective TCZ study were documented by 13 centers. RESULTS: From 7/2009 to 4/2014, 200 patients with sJIA were recorded in the AID-registry. Out of these, 46 (19 m, 27 f, age 1–18 years) received therapy with TCZ. Long term treatment (median 23 months) has been documented in 24/46 patients who were evaluated according to Wallace criteria (active disease 6/24, inactive disease 5/24, remission 13/24 cases). Under observation co-medication were used in 40/46 cases. Adverse events were reported in 11/46 patients. The clinical response rate (no clinical manifestation, no increased inflammation parameters) within the first 12 weeks of treatment was calculated to be 35%. CONCLUSION: Out of 200 sJIA children reported in the German AID-registry, 46 were treated with TCZ, showing a clinical response rate of 35% during the first 12 weeks, and inactive disease and/or remission under medication in 75% after one year. Adverse events were seen in 24% and severe adverse events in 4%. TRIAL REGISTRATION: The AID-Registry is funded by the BMBF (01GM08104, 01GM1112D, 01GM1512D). |
format | Online Article Text |
id | pubmed-5887199 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-58871992018-04-09 IL-6 blockade in systemic juvenile idiopathic arthritis – achievement of inactive disease and remission (data from the German AID-registry) Bielak, M. Husmann, E. Weyandt, N. Haas, J.-P. Hügle, B. Horneff, G. Neudorf, U. Lutz, T. Lilienthal, E. Kallinich, T. Tenbrock, K. Berendes, R. Niehues, T. Wittkowski, H. Weißbarth-Riedel, E. Heubner, G. Oommen, P. Klotsche, J. Foell, Dirk Lainka, E. Pediatr Rheumatol Online J Research Article BACKGROUND: Systemic juvenile idiopathic arthritis (sJIA) is a complex disease with an autoinflammatory component of unknown etiology related to the innate immune system. A major role in the pathogenesis has been ascribed to proinflammatory cytokines like interleukin-6 (IL-6), and effective drugs inhibiting their signaling are being developed. This study evaluates sJIA patients treated with the IL-6 inhibitor tocilizumab (TCZ) concerning clinical response rate, disease course and adverse effects in a real-life clinical setting. METHODS: In 2009 a clinical and research consortium was established, including an online registry for autoinflammatory diseases (AID) (https://aid-register.de). Data for this retrospective TCZ study were documented by 13 centers. RESULTS: From 7/2009 to 4/2014, 200 patients with sJIA were recorded in the AID-registry. Out of these, 46 (19 m, 27 f, age 1–18 years) received therapy with TCZ. Long term treatment (median 23 months) has been documented in 24/46 patients who were evaluated according to Wallace criteria (active disease 6/24, inactive disease 5/24, remission 13/24 cases). Under observation co-medication were used in 40/46 cases. Adverse events were reported in 11/46 patients. The clinical response rate (no clinical manifestation, no increased inflammation parameters) within the first 12 weeks of treatment was calculated to be 35%. CONCLUSION: Out of 200 sJIA children reported in the German AID-registry, 46 were treated with TCZ, showing a clinical response rate of 35% during the first 12 weeks, and inactive disease and/or remission under medication in 75% after one year. Adverse events were seen in 24% and severe adverse events in 4%. TRIAL REGISTRATION: The AID-Registry is funded by the BMBF (01GM08104, 01GM1112D, 01GM1512D). BioMed Central 2018-04-05 /pmc/articles/PMC5887199/ /pubmed/29622022 http://dx.doi.org/10.1186/s12969-018-0236-y Text en © The Author(s). 2018 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated. |
spellingShingle | Research Article Bielak, M. Husmann, E. Weyandt, N. Haas, J.-P. Hügle, B. Horneff, G. Neudorf, U. Lutz, T. Lilienthal, E. Kallinich, T. Tenbrock, K. Berendes, R. Niehues, T. Wittkowski, H. Weißbarth-Riedel, E. Heubner, G. Oommen, P. Klotsche, J. Foell, Dirk Lainka, E. IL-6 blockade in systemic juvenile idiopathic arthritis – achievement of inactive disease and remission (data from the German AID-registry) |
title | IL-6 blockade in systemic juvenile idiopathic arthritis – achievement of inactive disease and remission (data from the German AID-registry) |
title_full | IL-6 blockade in systemic juvenile idiopathic arthritis – achievement of inactive disease and remission (data from the German AID-registry) |
title_fullStr | IL-6 blockade in systemic juvenile idiopathic arthritis – achievement of inactive disease and remission (data from the German AID-registry) |
title_full_unstemmed | IL-6 blockade in systemic juvenile idiopathic arthritis – achievement of inactive disease and remission (data from the German AID-registry) |
title_short | IL-6 blockade in systemic juvenile idiopathic arthritis – achievement of inactive disease and remission (data from the German AID-registry) |
title_sort | il-6 blockade in systemic juvenile idiopathic arthritis – achievement of inactive disease and remission (data from the german aid-registry) |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5887199/ https://www.ncbi.nlm.nih.gov/pubmed/29622022 http://dx.doi.org/10.1186/s12969-018-0236-y |
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