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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...

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Autores principales: 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.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2018
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).
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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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