Association between enthesitis/dactylitis resolution and patient-reported outcomes in guselkumab-treated patients with psoriatic arthritis.

Journal: Clinical rheumatology

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Affiliated Institutions:  Memorial University of Newfoundland, St. Johns, NF, Canada. University of Glasgow, Glasgow, UK. Oregon Health & Science University, Portland, OR, USA. FAU Erlangen-Nürnberg and Universitätsklinikum, Erlangen, Germany. Rheumatology Research, Providence Swedish Medical Center, Seattle, WA, USA. Janssen Research & Development, LLC, Titusville, NJ, USA. Janssen Research & Development, LLC, Spring House, PA, USA. Janssen Research & Development, LLC, San Diego, CA, USA. University of Rochester Medical Center, Rochester, NY, USA. Leeds Biomedical Research Centre, University of Leeds, nd Floor, Chapel Allerton Hospital, Chapeltown Road, Leeds, LS SA, UK. D.G.McGonagle@leeds.ac.uk.

Abstract summary 

To evaluate the association between enthesitis resolution (ER) and dactylitis resolution (DR) and meaningful improvements in patient-reported outcomes (PROs) among biologic-naïve patients with PsA receiving guselkumab in the DISCOVER-2 study.Enthesitis and dactylitis, characteristic lesions of PsA, were evaluated by independent assessors using the Leeds Enthesitis Index (range, 0-6) and Dactylitis Severity Score (range, 0-60). Proportions of patients with ER or DR (score = 0) among those with score > 0 at baseline were determined at weeks 24, 52, and 100. PROs included: fatigue (Functional Assessment of Chronic Illness Therapy-Fatigue [FACIT-Fatigue]), pain (0-100 visual analog scale), physical function (Health Assessment Questionnaire-Disability Index [HAQ-DI]), and health-related quality of life (36-item Short-Form Health Survey physical/mental component summary [SF-36 PCS/MCS]). Meaningful responses were defined as: improvements of ≥ 4 for FACIT-Fatigue, ≥ 0.35 for HAQ-DI, and ≥ 5 for SF-36 PCS/MCS and absolute scores of ≤ 15 for minimal pain and ≤ 0.5 for normalized HAQ-DI. Associations between ER/DR status and PRO response status were tested using a Chi-square test.Guselkumab-treated patients with ER were more likely than those without ER to achieve minimal pain (p < 0.001), normalized HAQ-DI (p < 0.001), and PCS response (p < 0.05) at weeks 24, 52, and 100. Patients with DR were more likely than those without DR to achieve FACIT-Fatigue response at week 24 and week 52 (both p ≤ 0.01) and minimal pain at week 24 and normalized HAQ-DI at week 52 (both p ≤ 0.03).In biologic-naïve patients with active PsA treated with guselkumab, achieving ER or DR was associated with durable improvements in selected PROs, including those of high importance to patients.ClinicalTrials.gov ( https://clinicaltrials.gov ) NCT03158285; Registered: May 16, 2017. Key Points • At week 100, 65% and 76% of guselkumab-treated patients achieved enthesitis and dactylitis resolution (ER/DR). • Achieving ER was associated with achieving DR and vice versa through the end of study. • Achieving ER or DR was associated with durable and meaningful improvements in selected patient-reported outcomes.

Authors & Co-authors:  Rahman McInnes Deodhar Schett Mease Shawi Cua Sherlock Kollmeier Xu Sheng Ritchlin McGonagle

Study Outcome 

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Citations :  Ritchlin CT, Colbert RA, Gladman DD (2017) Psoriatic arthritis. N Engl J Med 376(10):957–970
Authors :  13
Identifiers
Doi : 10.1007/s10067-024-06921-8
SSN : 1434-9949
Study Population
Male,Female
Mesh Terms
Other Terms
Biologic;Dactylitis;Enthesitis;Guselkumab;Psoriatic arthritis
Study Design
Study Approach
Country of Study
Mali
Publication Country
Germany