PERFECTRA: a pragmatic, multicentre, real-life study comparing treat-to-target strategies with baricitinib versus TNF inhibitors in patients with active rheumatoid arthritis after failure on csDMARDs

ObjectiveTo compare the effectiveness of a strategy administering baricitinib versus one using TNF-inhibitors (TNFi) in patients with rheumatoid arthritis (RA) after conventional synthetic disease-modifying antirheumatic drugs (csDMARDs) failure in a real-life treat-to-target (T2T) setting.MethodsPa...

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Veröffentlicht in:Rheumatic & musculoskeletal diseases open 2024-05, Vol.10 (2), p.e004291
Hauptverfasser: van de Laar, Celine J, Oude Voshaar, Martijn A H, ten Klooster, Peter, Tedjo, Danyta I, Bos, Reinhard, Jansen, Tim, Willemze, A, Versteeg, Grada A, Goekoop-Ruiterman, Y P M, Kroot, Eric-Jan, van de Laar, Mart
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Sprache:eng
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Zusammenfassung:ObjectiveTo compare the effectiveness of a strategy administering baricitinib versus one using TNF-inhibitors (TNFi) in patients with rheumatoid arthritis (RA) after conventional synthetic disease-modifying antirheumatic drugs (csDMARDs) failure in a real-life treat-to-target (T2T) setting.MethodsPatients with biological and targeted synthetic DMARD (b/tsDMARD) naïve RA with disease duration ≤5 years without contraindications to b/tsDMARD were randomised to either TNFi or baricitinib when csDMARD failed to achieve disease control in a T2T setting. Changes in clinical and patient-reported outcome measures (PROMs) were assessed at 12-week intervals for 48 weeks. The primary endpoint was non-inferiority, with testing for superiority if non-inferiority is demonstrated, of baricitinib strategy in the number of patients achieving American College of Rheumatology 50 (ACR50) response at 12 weeks. Secondary endpoints included 28-joint count Disease Activity Score with C reactive protein (DAS28-CRP)
ISSN:2056-5933
2056-5933
DOI:10.1136/rmdopen-2024-004291