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IL-6 blockade in systemic juvenile idiopathic arthritis – achievement of inactive disease and remission (data from the German AID-registry).

Authors :
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.
Source :
Pediatric Rheumatology. 4/5/2018, Vol. 16, p1-1. 1p.
Publication Year :
2018

Abstract

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) (<ext-link>https://aid-register.de</ext-link>). 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). [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
15460096
Volume :
16
Database :
Academic Search Index
Journal :
Pediatric Rheumatology
Publication Type :
Academic Journal
Accession number :
128896608
Full Text :
https://doi.org/10.1186/s12969-018-0236-y