Continuous improvement through differential trajectories of individual minimal disease activity criteria with guselkumab in active psoriatic arthritis: post hoc analysis of a phase 3, randomized, double-blind, placebo-controlled study

被引:0
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作者
Coates, Laura C. [1 ]
Rahman, Proton [2 ,3 ]
Mease, Philip J. [4 ]
Shawi, May [5 ]
Rampakakis, Emmanouil [6 ,7 ]
Kollmeier, Alexa P. [8 ]
Xu, Xie L. [8 ]
Chakravarty, Soumya D. [9 ,10 ]
McInnes, Iain B. [11 ]
Tam, Lai-Shan [12 ]
机构
[1] Univ Oxford, Nuffield Dept Orthopaed Rheumatol & Musculoskelet, Oxford, England
[2] Craig L Dobbin Genet Res Ctr, St John, NF, Canada
[3] Mem Univ Newfoundland, St John, NF, Canada
[4] Univ Washington, Swedish Med Ctr, Dept Rheumatol Res, Providence St Joseph Hlth, Seattle, WA USA
[5] Janssen Res & Dev LLC, Titusville, NJ USA
[6] McGill Univ, Dept Pediat, Montreal, PQ, Canada
[7] JSS Med Res Inc, Sci Affairs, Montreal, PQ, Canada
[8] Janssen Res & Dev LLC, Immunol, San Diego, CA USA
[9] Janssen Sci Affairs LLC, Horsham, PA USA
[10] Drexel Univ, Coll Med, Div Rheumatol, Philadelphia, PA USA
[11] Univ Glasgow, Coll Med Vet & Life Sci, Glasgow, Lanark, Scotland
[12] Chinese Univ Hong Kong, Dept Med & Therapeut, Sha Tin, Hong Kong, Peoples R China
关键词
Psoriatic arthritis; Biologics; Guselkumab; Minimal disease activity; RHEUMATOID-ARTHRITIS; THERAPY; FATIGUE;
D O I
10.1186/s41927-024-00375-w
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Background To explore the trajectory of, and factors contributing to, achievement of individual criteria of minimal disease activity (MDA) in patients with active psoriatic arthritis (PsA) treated with guselkumab. Methods The Phase 3, randomized, placebo-controlled DISCOVER-2 study enrolled adults (N = 739) with active PsA despite standard therapies who were biologic/Janus kinase inhibitornaive. Patients were randomized 1:1:1 to guselkumab 100 mg every 4 weeks; guselkumab 100 mg at week 0, week 4, then every 8 weeks; or placebo. In this post hoc analysis, patients randomized to guselkumab were included and pooled (N = 493). Longitudinal trajectories of achieving each MDA criterion through week 100 were derived using non-responder imputation. Time to achieve each criterion was estimated with Kaplan-Meier analysis. Multivariate regression for time to achieve each criterion (Cox regression) and achievement at week 100 (logistic regression) was used to identify contributing factors. Results Continuous improvement across all MDA domains was shown over time. similar to 70% of patients achieved near remission in swollen joint count (SJC), Psoriasis Area and Severity Index (PASI), and enthesitis through week 100. Median times to achieve individual criteria differed significantly (p < 0.0001), with SJC <= 1 (20 weeks), PASI <= 1 (16 weeks), and <= 1 tender entheses (16 weeks) being faster than patient-reported criteria (pain <= 15 mm, patient global assessment of arthritis and psoriasis <= 20 mm, Health Assessment Questionnaire-Disability Index <= 0.5) and tender joint count <= 1. Higher baseline domain scores, older age, worse fatigue, and increased body mass index were significant predictors of longer time to achieve minimal levels of disease activity assessed via patient-reported criteria. Conclusions Continuous improvement across all MDA domains was shown over time. similar to 70% of patients achieved near remission in swollen joint count (SJC), Psoriasis Area and Severity Index (PASI), and enthesitis through week 100. Median times to achieve individual criteria differed significantly (p < 0.0001), with SJC <= 1 (20 weeks), PASI <= 1 (16 weeks), and <= 1 tender entheses (16 weeks) being faster than patient-reported criteria (pain <= 15 mm, patient global assessment of arthritis and psoriasis <= 20 mm, Health Assessment Questionnaire-Disability Index <= 0.5) and tender joint count <= 1. Higher baseline domain scores, older age, worse fatigue, and increased body mass index were significant predictors of longer time to achieve minimal levels of disease activity assessed via patient-reported criteria. Trial registration number NCT03158285. Trial registration date May 16, 2017.
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