Performance of the 2016 ACR-EULAR myositis response criteria in juvenile dermatomyositis therapeutic trials and consensus profiles.


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
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

3680-3689

Subventions

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.

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Auteurs

Hanna Kim (H)

Juvenile Myositis Pathogenesis and Therapeutics Unit, National Institute of Arthritis Musculoskeletal and Skin Diseases, National Institutes of Health (NIH), Bethesda, MD, USA.

Didem Saygin (D)

Section of Rheumatology, Department of Medicine, University of Chicago, Chicago, IL, USA.
School of Medicine, Division of Rheumatology and Clinical Immunology, University of Pittsburgh, Pittsburgh, PA, USA.

Christian Douglas (C)

Social & Scientific Systems, Inc, Durham, NC, USA.

Jesse Wilkerson (J)

Social & Scientific Systems, Inc, Durham, NC, USA.

Brian Erman (B)

Social & Scientific Systems, Inc, Durham, NC, USA.

Angela Pistorio (A)

IRCCS Istituto Giannina Gaslini, Direzione Scientifica, Genoa, Italy.

John A McGrath (JA)

Social & Scientific Systems, Inc, Durham, NC, USA.

Ann M Reed (AM)

Department of Pediatrics, Duke University, Durham, NC, USA.

Chester V Oddis (CV)

School of Medicine, Division of Rheumatology and Clinical Immunology, University of Pittsburgh, Pittsburgh, PA, USA.

Claudia Bracaglia (C)

Division of Rheumatology, IRCCS Ospedale Pediatrico Bambino Gesù, Roma, Italy.

Annet van Royen-Kerkhof (A)

Department of Pediatric Immunology and Rheumatology, Wilhelmina Children's Hospital, Utrecht, The Netherlands.

Blanca Bica (B)

Section of Rheumatology, Department of Internal Medicine, Universidade Federal do Rio de Janeiro, Rio de Janeiro, Brazil.

Pavla Dolezalova (P)

General University Hospital and 1st Faculty of Medicine, Charles University, Prague, Czech Republic.

Virginia P L Ferriani (VPL)

Department of Pediatrics; Division of Rheumatology, Ribeirao Preto Medical School- Sao Paulo University, Ribeirao Preto, Brazil.

Berit Flato (B)

Department of Rheumatology, Oslo University Hospital, Norway and Institute of clinical medicine, University of Oslo, Oslo, Norway.

Ana G Bernard-Medina (AG)

Hospital Civil de Guadalajara FrayAntonio Alcalde, Guadalajara, Mexico.

Troels Herlin (T)

Pediatrics and Adolescent Medicine, Aarhus University Hospital, Aarhus, Denmark.

Frederick W Miller (FW)

Environmental Autoimmunity Group, Clinical Research Branch, National Institute of Environmental Health Sciences, NIH, Bethesda, MD, USA.

Jiri Vencovsky (J)

Institute of Rheumatology, Department of Rheumatology, Charles University, Prague, Czech Republic.

Nicolino Ruperto (N)

UOSID Centro Trial, PRINTO, IRCCS Istituto Giannina Gaslini, Genova, Italy.

Rohit Aggarwal (R)

School of Medicine, Division of Rheumatology and Clinical Immunology, University of Pittsburgh, Pittsburgh, PA, USA.

Lisa G Rider (LG)

Environmental Autoimmunity Group, Clinical Research Branch, National Institute of Environmental Health Sciences, NIH, Bethesda, MD, USA.

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