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Performance of the 2016 ACR-EULAR myositis response criteria in juvenile dermatomyositis therapeutic trials and consensus profiles.
Kim, Hanna; Saygin, Didem; Douglas, Christian; Wilkerson, Jesse; Erman, Brian; Pistorio, Angela; McGrath, John A; Reed, Ann M; Oddis, Chester V; Bracaglia, Claudia; van Royen-Kerkhof, Annet; Bica, Blanca; Dolezalova, Pavla; Ferriani, Virginia P L; Flato, Berit; Bernard-Medina, Ana G; Herlin, Troels; Miller, Frederick W; Vencovsky, Jiri; Ruperto, Nicolino; Aggarwal, Rohit; Rider, Lisa G.
Affiliation
  • Kim H; Juvenile Myositis Pathogenesis and Therapeutics Unit, National Institute of Arthritis Musculoskeletal and Skin Diseases, National Institutes of Health (NIH), Bethesda, MD, USA.
  • Saygin D; Section of Rheumatology, Department of Medicine, University of Chicago, Chicago, IL, USA.
  • Douglas C; School of Medicine, Division of Rheumatology and Clinical Immunology, University of Pittsburgh, Pittsburgh, PA, USA.
  • Wilkerson J; Social & Scientific Systems, Inc, Durham, NC, USA.
  • Erman B; Social & Scientific Systems, Inc, Durham, NC, USA.
  • Pistorio A; Social & Scientific Systems, Inc, Durham, NC, USA.
  • McGrath JA; IRCCS Istituto Giannina Gaslini, Direzione Scientifica, Genoa, Italy.
  • Reed AM; Social & Scientific Systems, Inc, Durham, NC, USA.
  • Oddis CV; Department of Pediatrics, Duke University, Durham, NC, USA.
  • Bracaglia C; School of Medicine, Division of Rheumatology and Clinical Immunology, University of Pittsburgh, Pittsburgh, PA, USA.
  • van Royen-Kerkhof A; Division of Rheumatology, IRCCS Ospedale Pediatrico Bambino Gesù, Roma, Italy.
  • Bica B; Department of Pediatric Immunology and Rheumatology, Wilhelmina Children's Hospital, Utrecht, The Netherlands.
  • Dolezalova P; Section of Rheumatology, Department of Internal Medicine, Universidade Federal do Rio de Janeiro, Rio de Janeiro, Brazil.
  • Ferriani VPL; General University Hospital and 1st Faculty of Medicine, Charles University, Prague, Czech Republic.
  • Flato B; Department of Pediatrics; Division of Rheumatology, Ribeirao Preto Medical School- Sao Paulo University, Ribeirao Preto, Brazil.
  • Bernard-Medina AG; Department of Rheumatology, Oslo University Hospital, Norway and Institute of clinical medicine, University of Oslo, Oslo, Norway.
  • Herlin T; Hospital Civil de Guadalajara FrayAntonio Alcalde, Guadalajara, Mexico.
  • Miller FW; Pediatrics and Adolescent Medicine, Aarhus University Hospital, Aarhus, Denmark.
  • Vencovsky J; Environmental Autoimmunity Group, Clinical Research Branch, National Institute of Environmental Health Sciences, NIH, Bethesda, MD, USA.
  • Ruperto N; Institute of Rheumatology, Department of Rheumatology, Charles University, Prague, Czech Republic.
  • Aggarwal R; UOSID Centro Trial, PRINTO, IRCCS Istituto Giannina Gaslini, Genova, Italy.
  • Rider LG; School of Medicine, Division of Rheumatology and Clinical Immunology, University of Pittsburgh, Pittsburgh, PA, USA.
Rheumatology (Oxford) ; 62(11): 3680-3689, 2023 11 02.
Article in En | MEDLINE | ID: mdl-36929918
OBJECTIVES: 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. METHODS: 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. RESULTS: 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). CONCLUSION: The ACR-EULAR MRC perform consistently across multiple studies, supporting its further use as an efficacy end point in JDM trials.
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Dermatomyositis / Myositis Limits: Humans Language: En Journal: Rheumatology (Oxford) Journal subject: REUMATOLOGIA Year: 2023 Document type: Article Affiliation country: Estados Unidos Country of publication: Reino Unido

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Dermatomyositis / Myositis Limits: Humans Language: En Journal: Rheumatology (Oxford) Journal subject: REUMATOLOGIA Year: 2023 Document type: Article Affiliation country: Estados Unidos Country of publication: Reino Unido