Performance of the 2016 ACR-EULAR myositis response criteria in juvenile dermatomyositis therapeutic trials and consensus profiles.
JDM
clinical trial
myositis
outcome assessment
outcome measure
response criteria
Journal
Rheumatology (Oxford, England)
ISSN: 1462-0332
Titre abrégé: Rheumatology (Oxford)
Pays: England
ID NLM: 100883501
Informations de publication
Date de publication:
02 11 2023
02 11 2023
Historique:
received:
14
12
2022
accepted:
24
02
2023
medline:
9
11
2023
pubmed:
18
3
2023
entrez:
17
3
2023
Statut:
ppublish
Résumé
The 2016 ACR-EULAR Response Criteria for JDM was developed as a composite measure with differential weights of six core set measures (CSMs) to calculate a Total Improvement Score (TIS). We assessed the contribution of each CSM, representation of muscle-related and patient-reported CSMs towards improvement, and frequency of CSM worsening across myositis response criteria (MRC) categories in validation of MRC. Data from JDM patients in the Rituximab in Myositis trial (n = 48), PRINTO JDM trial (n = 139), and consensus patient profiles (n = 273) were included. Observed vs expected CSM contributions were compared using Sign test. Characteristics of MRC categories were compared by Wilcoxon tests with Bonferroni adjustment. Spearman correlation of changes in TIS and individual CSMs were examined. Agreement between physician-assessed change and MRC categories was evaluated by weighted Cohen's kappa. Of 457 JDM patients with IMACS CSMs and 380 with PRINTO CSMs, 9-13% had minimal, 19-23% had moderate and 41-50% had major improvement. The number of improved and absolute percentage change of CSMs increased by MRC improvement level. Patients with minimal improvement by MRC had a median of 0-1 CSM worsened, and those with moderate/major improvement had a median of zero worsening CSMs. Of patients improved by MRC, 94-95% had improvement in muscle strength and 93-95% had improvement in ≥1 patient-reported CSM. IMACS and PRINTO CSMs performed similarly. Physician-rated change and MRC improvement categories had moderate-to-substantial agreement (Kappa 0.5-0.7). The ACR-EULAR MRC perform consistently across multiple studies, supporting its further use as an efficacy end point in JDM trials.
Identifiants
pubmed: 36929918
pii: 7079790
doi: 10.1093/rheumatology/kead111
pmc: PMC10629769
doi:
Substances chimiques
Rituximab
4F4X42SYQ6
Types de publication
Journal Article
Research Support, Non-U.S. Gov't
Research Support, N.I.H., Intramural
Langues
eng
Sous-ensembles de citation
IM
Pagination
3680-3689Subventions
Organisme : NIEHS NIH HHS
ID : HHSN273201600002C
Pays : United States
Organisme : Intramural NIH HHS
ID : ZIA AR041215
Pays : United States
Organisme : NIEHS NIH HHS
ID : HHSN273201600002I
Pays : United States
Organisme : Intramural NIH HHS
ID : ZIA ES101081
Pays : United States
Investigateurs
Iago Pinal-Fernandez
(I)
Susan Kim
(S)
Dana Ascherman
(D)
Adam Schiffenbauer
(A)
Informations de copyright
Published by Oxford University Press on behalf of the British Society for Rheumatology 2023.
Références
J Rheumatol. 1986 Apr;13(2):349-55
pubmed: 3723497
Pediatr Rheumatol Online J. 2017 Jan 11;15(1):1
pubmed: 28077146
Arthritis Rheum. 2008 Jan 15;59(1):4-13
pubmed: 18163404
Arthritis Rheum. 2005 Sep;52(9):2607-15
pubmed: 16142757
Biometrics. 1977 Mar;33(1):159-74
pubmed: 843571
Arthritis Rheum. 1997 Nov;40(11):1976-83
pubmed: 9365086
Arthritis Rheum. 2004 Jul;50(7):2281-90
pubmed: 15248228
Rheum Dis Clin North Am. 2021 Nov;47(4):669-690
pubmed: 34635298
Rheumatology (Oxford). 2017 Nov 1;56(11):1884-1893
pubmed: 28977549
ACR Open Rheumatol. 2022 Aug;4(8):671-681
pubmed: 35616642
Arthritis Rheumatol. 2017 May;69(5):911-923
pubmed: 28382778
Arthritis Rheum. 2013 Feb;65(2):314-24
pubmed: 23124935
Lancet. 2016 Feb 13;387(10019):671-678
pubmed: 26645190
Clin Exp Rheumatol. 2022 Feb;40(2):394-403
pubmed: 35225221
Arthritis Care Res (Hoboken). 2011 Nov;63 Suppl 11:S118-57
pubmed: 22588740
Ann Rheum Dis. 2021 Mar;80(3):406-408
pubmed: 32843325