dc.contributor.author
Horneff, Gerd
dc.contributor.author
Klein, Ariane
dc.contributor.author
Klotsche, Jens
dc.contributor.author
Minden, Kirsten
dc.contributor.author
Huppertz, Hans-Iko
dc.contributor.author
Weller-Heinemann, Frank
dc.contributor.author
Kuemmerle-Deschner, Jasmin
dc.contributor.author
Haas, Johannes-Peter
dc.contributor.author
Hospach, Anton
dc.date.accessioned
2018-06-08T10:48:52Z
dc.date.available
2017-01-12T12:28:51.186Z
dc.identifier.uri
https://refubium.fu-berlin.de/handle/fub188/21136
dc.identifier.uri
http://dx.doi.org/10.17169/refubium-24433
dc.description.abstract
Background Treatment response, remission rates and compliance in patients with
polyarticular juvenile idiopathic arthritis (polyJIA) treated with adalimumab,
etanercept, or tocilizumab were analyzed in clinical practice. Methods Data
collected in the German BIKER registry were analyzed in patients with polyJIA
who started treatment with approved biologics, adalimumab, etanercept or
tocilizumab, from 2011 to 2015. Baseline patient characteristics, treatment
response, safety and drug survival were compared. Results Two hundred thirty-
six patient started adalimumab, 419 etanercept and 74 tocilizumab, with
differences in baseline patient characteristics. Baseline Juvenile Disease
Activity Score (JADAS)10 (mean ± SD) in the adalimumab/etanercept/tocilizumab
cohorts was 12.1+/−7.6, 13.8 ± 7.1 and 15.1 ± 7.4, respectively (adalimumab vs
etanercept, p = 0.01), and Childhood Health Assessment Questionnaire
(CHAQ)-disability index scores was 0.43 ± 0.58, 0.59 ± 0.6 and 0.63 ± 0.55,
respectively (adalimumab vs etanercept, p < 0.001). Uveitis history was more
frequent in the adalimumab cohort (OR 5.73; p < 0.001). Balanced patients’
samples were obtained by a generalized propensity score to adjust for baseline
differences. Pediatric ACR30/50/70/90 criterion improvement after 3 months
treatment was achieved by 68%/60%/42%/24% in the etanercept cohort,
67%/59%/43%/27% in the adalimumab cohort and 61%/52%/35%/26% in the
tocilizumab cohort. At 24 months, JADAS minimal disease activity was achieved
in 52.4%/61.3%/52.4% and JADAS remission in 27.9%/34.8%/27.9% patients in the
adalimumab/etanercept/tocilizumab cohorts, respectively. Etanercept was used
in 95.5% of patients as a first biologic, adalimumab in 50.8% and tocilizumab
in 20.2%. There were no important differences in efficacy between first-line
and second-line use of biologics. In total 60.4%/49.4%/31.1% patients
discontinued adalimumab/etanercept/tocilizumab, respectively (HR for
adalimumab 1.67; p < 0.001; HR for tocilizumab 0.35; p = 0.001). Drug survival
rates did not differ significantly in patients on biologic monotherapy
compared with combination therapy with methotrexate. Over 4 years observation
under etanercept/adalimumab/tocilizumab, 996/386/103 adverse events, and
148/119/26 serious adverse events, respectively, were reported. Conclusions In
clinical practice, etanercept is most frequently used as first-line biologic.
Adalimumab/etanercept/tocilizumab showed comparable efficacy toward polyJIA.
Overall, tolerance was acceptable. Interestingly, compliance was highest with
tocilizumab and lowest with adalimumab. This study provides the first
indication for the comparison of different biologic agents in polyarticular
JIA based on observational study data with all their weaknesses and
demonstrates the need for well-controlled head-to-head studies for
confirmation.
en
dc.rights.uri
http://creativecommons.org/licenses/by/4.0/
dc.subject
Juvenile idiopathic arthritis
dc.subject
Drug surveillance
dc.subject.ddc
600 Technik, Medizin, angewandte Wissenschaften::610 Medizin und Gesundheit
dc.title
Comparison of treatment response, remission rate and drug adherence in
polyarticular juvenile idiopathic arthritis patients treated with etanercept,
adalimumab or tocilizumab
dc.type
Wissenschaftlicher Artikel
dcterms.bibliographicCitation
Arthritis Research & Therapy. - 18 (2016), Artikel Nr. 272
dcterms.bibliographicCitation.doi
10.1186/s13075-016-1170-3
dcterms.bibliographicCitation.url
http://arthritis-research.biomedcentral.com/articles/10.1186/s13075-016-1170-3
refubium.affiliation
Charité - Universitätsmedizin Berlin
de
refubium.mycore.fudocsId
FUDOCS_document_000000026134
refubium.note.author
Der Artikel wurde in einer reinen Open-Access-Zeitschrift publiziert.
refubium.resourceType.isindependentpub
no
refubium.mycore.derivateId
FUDOCS_derivate_000000007521
dcterms.accessRights.openaire
open access