Comparative performance of composite measures from two phase III clinical trials of ixekizumab in psoriatic arthritis.
Document Type
Article
Publication Date
9-1-2022
Publication Title
RMD Open
Keywords
washington; swedish; Antibodies, Monoclonal, Humanized; Antirheumatic Agents; Arthritis, Psoriatic; Disease Progression; Humans; Severity of Illness Index; Treatment Outcome
Abstract
BACKGROUND/OBJECTIVE: The aim of this study was to evaluate relative performance of composite measures in psoriatic arthritis and assess the impact of structural damage and functional disability on outcomes during ixekizumab treatment.
METHODS: Data from SPIRIT-P1 and SPIRIT-P2 were analysed to evaluate the effect of ixekizumab on achievement of low disease activity (LDA) and remission with the minimal disease activity (MDA) and very low disease activity (VLDA) composite, Disease Activity index for Psoriatic Arthritis (DAPSA), Psoriatic Arthritis Disease Activity Score, GRAppa Composite ScorE and modified Composite Psoriatic Disease Activity Index (mCPDAI). Performance was compared by quantifying residual symptom burden and the impact of structural damage and functional disability.
RESULTS: Significantly more ixekizumab-treated patients achieved treatment targets at week 24 versus placebo assessed with all composites. More patients achieved targets assessed by mCPDAI and DAPSA than other composites. Residual disease activity was similar between composites, but residual high patient-reported outcomes (PROs) and functional disability were more frequent when assessed with mCPDAI and DAPSA. Achievement of treatment targets was reduced by high baseline levels of structural damage and functional disability.
CONCLUSION: Residual disease activity was similar in patients achieving treatment targets assessed with all composites, but residual high PROs and functional disability were more common when assessed with mCPDAI and DAPSA, most likely due to the absence/attenuated functional assessment in these composites. High baseline levels of structural damage and functional disability attenuated response rates with all composites, affecting MDA/VLDA most prominently; LDA may be the most appropriate target in these patients.
TRIAL REGISTRATION NUMBER: NCT01695239.
Clinical Institute
Orthopedics & Sports Medicine
Department
Orthopedics
Department
Rheumatology
Recommended Citation
Coates, Laura C; Smolen, Josef S; Mease, Philip; Husni, M Elaine; Merola, Joseph F; Lespessailles, Eric; Kishimoto, Mitsumasa; Macpherson, Lisa; Bradley, Andrew J; Bolce, Rebecca; and Helliwell, Philip S, "Comparative performance of composite measures from two phase III clinical trials of ixekizumab in psoriatic arthritis." (2022). Articles, Abstracts, and Reports. 6758.
https://digitalcommons.providence.org/publications/6758
