Children With Enthesitis-Related Arthritis and Possible Benefits From Treatments for Adults With Spondyloarthritis.
Children With Enthesitis-Related Arthritis and Possible Benefits From Treatments for Adults With Spondyloarthritis.
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DOI:
10.1002/acr.24529
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发表时间:
2022-07
影响因子:
4.7
通讯作者:
PRCSG Advisory Council and the CARRA Executive Committee
中科院分区:
文献类型:
--
作者:
Weiss PF;Fuhlbrigge RC;von Scheven E;Lovell DJ;Colbert RA;Brunner HI;PRCSG Advisory Council and the CARRA Executive Committee
This review will summarize clinical, genetic and pathophysiologic characteristics that are shared between children with enthesitis related arthritis (ERA) with axial involvement and adults with non-radiographic, and in some cases radiographic, axial spondyloarthritis (SpA); and between children with ERA and primarily peripheral disease manifestations and adults with peripheral SpA. Due to the differences in classification criteria for children with ERA and adults with axial and peripheral SpA, the FDA granted automatic full waivers of studies in children for new medications for “axial spondyloarthropathies including ankylosing spondylitis” up until July 2020. Thus, although current juvenile idiopathic arthritis (JIA) treatment guidelines recommend the use of biologic disease modifying anti-rheumatic drugs (DMARDs) as part of the early treatment for patients with ERA, none of the FDA-approved therapies for peripheral SpA or non-radiographic axial SpA (certolizumab pegol, ixekizumab, and secukinumab) have been studied or are labelled for use in children with ERA. Considering the similarities between adult spondyloarthritis and ERA in terms of etiology, genetics, pathogenesis and clinical manifestations summarized in this review, medications approved for axial SpA or peripheral SpA should also be studied in children with active ERA involving axial or peripheral joints, respectively, with the intent to achieve labeling for use in children. Considering the current lack of effective FDA-approved therapies for ERA, the FDA should also consider requiring pediatric studies for medications that have already been approved for the treatment of adults with SpA.
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影响因子:
27.4
作者:
Carron, Philippe;Varkas, Gaelle;Van den Bosch, Filip
通讯作者:
Van den Bosch, Filip
影响因子:
2.1
作者:
Lee, Edward Y.;Sundel, Robert P.;Kleinman, Paul K.
通讯作者:
Kleinman, Paul K.
影响因子:
4.9
作者:
Gmuca S;Xiao R;Brandon TG;Pagnini I;Wright TB;Beukelman T;Morgan EM;Weiss PF
通讯作者:
Weiss PF
DOI:
10.1186/s12969-018-0238-9
发表时间:
2018-04-02
期刊:
Pediatric rheumatology online journal
影响因子:
--
作者:
Goirand M;Breton S;Chevallier F;Duong NP;Uettwiller F;Melki I;Mouy R;Wouters C;Bader-Meunier B;Job-Deslandre C;Quartier P
通讯作者:
Quartier P
影响因子:
168.9
作者:
Deodhar, Atul;van der Heijde, Desiree;Sieper, Joachim
通讯作者:
Sieper, Joachim