Feasibility of Conducting Comparative Effectiveness Research and Validation of a Clinical Disease Activity Score for Chronic Nonbacterial Osteomyelitis

Author:

Wu Eveline Y.ORCID,Oliver Melissa,Scheck Joshua,Lapidus Sivia,Akca Ummusen Kaya,Yasin Shima,Stern Sara M.,Insalaco Antonella,Pardeo Manuela,Simonini Gabriele,Marrani Edoardo,Wang Xing,Huang BinORCID,Kovalick Leonard K.,Rosenwasser Natalie,Casselman Gabriel,Liau Adriel,Shao Yurong,Yang Claire,Mosa Doaa Mosad,Tucker Lori,Girschick Hermann,Laxer Ronald M.,Akikusa Jonathan D.,Hedrich Christian,Onel Karen,Dedeoglu Fatma,Twilt Marinka,Ferguson Polly J.,Ozen Seza,Zhao YongdongORCID

Abstract

AbstractIntroductionProspective comparative effectiveness research in chronic nonbacterial osteomyelitis (CNO) is lacking.ObjectivesStudy objectives were to: 1) determine the use and safety of each consensus treatment plan (CTP) regimen for CNO, 2) the feasibility of usingchronic nonbacterialosteomyelitis international registry (CHOIR) data for comparative effectiveness research, and 3) develop and validate a CNO clinical disease activity score (CDAS) using CHOIR.MethodsConsenting children or young adults with CNO were enrolled into CHOIR. Demographic, clinical, and imaging data were prospectively collected. The CNO CDAS was developed through a Delphi survey and nominal group technique. External validation surveys were administered to CHOIR participants.Results140 (76%) CHOIR participants enrolled between August 2018 and September 2020 received at least one CTP regimen. Baseline characteristics from the three groups were well matched. Patient pain, patient global assessment, and clinical CNO lesion count were key variables included in the CNO CDAS. The CDAS showed a strong correlation with patient/parent report of difficulty using a limb, back, or jaw and patient/parent report of disease severity, but a weak correlation with patient/parent report of fatigue, sadness, and worry. The change in CDAS was significant in patients reporting disease worsening or improvement. The CDAS significantly decreased after initiating second-line treatments from median 12 (8-15.5) to 5 (3-12). While second-line treatments were well tolerated, psoriasis was the most common adverse event.ConclusionThe CNO CDAS was developed and validated for disease monitoring and assessment of treatment effectiveness. CHOIR provided a comprehensive framework for future comparative effectiveness research.Key messagesThechronic nonbacterialosteomyelitis international registry (CHOIR) provides comprehensive prospective data for comparison of treatment effectivenessThe clinical disease activity score (CDAS) has content and construct validity to assess CNO

Publisher

Cold Spring Harbor Laboratory

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