Guselkumab, a Selective Interleukin‐23 p19 Subunit Inhibitor, Resolves Dactylitis in Patients With Active Psoriatic Arthritis: Pooled Results Through Week 52 From Two Phase 3 Studies

Author:

McGonagle Dennis1,McInnes Iain B.2ORCID,Deodhar Atul3ORCID,Schett Georg4ORCID,Shawi May5,Chakravarty Soumya D.6ORCID,Kollmeier Alexa P.7,Xu Xie L.7,Sheng Shihong8,Xu Stephen8,Ritchlin Christopher T.9ORCID,Rahman Proton10,Mease Phillip J.11ORCID

Affiliation:

1. Leeds Institute of Rheumatic and Musculoskeletal Medicine (LIRMM) University of Leeds; National Institute for Health Research (NIHR) Biomedical Research Centre Leeds UK

2. Institute of Infection, Immunity and Inflammation University of Glasgow Glasgow UK

3. Oregon Health and Science University Portland

4. Friedrich‐Alexander‐Universität Erlangen‐Nürnberg Erlangen Germany

5. Immunology Global Medical Affairs, Janssen Pharmaceutical Companies of Johnson & Johnson Horsham Pennsylvania

6. Janssen Scientific Affairs, LLC, Horsham, and Drexel University College of Medicine Philadelphia Pennsylvania

7. Janssen Research & Development, LLC San Diego California

8. Immunology Biostatistics, Janssen Research & Development, LLC Spring House Pennsylvania

9. University of Rochester Medical Center Rochester New York

10. Craig L. Dobbin Genetics Research Centre, Memorial University of Newfoundland St John's Newfoundland Canada

11. Swedish Medical Center/Providence St. Joseph Health and University of Washington School of Medicine Seattle Washington

Abstract

ObjectivePrevious analyses of pooled DISCOVER‐1 and DISCOVER‐2 data through Week 24 showed significantly higher rates of dactylitis resolution in patients treated with guselkumab compared with placebo. Here, we investigate associations between dactylitis resolution and other outcomes through 1 year.MethodsPatients were randomized 1:1:1 to receive subcutaneous injections of guselkumab 100 mg at Week 0, Week 4, and then every 4 or 8 weeks, or placebo with crossover to guselkumab at Week 24. Independent assessors determined dactylitis severity score (DSS; 0‐3/digit; total = 0‐60). Dactylitis resolution (DSS = 0) (prespecified) and at least 20%, at least 50%, and at least 70% DSS improvement from baseline (post hoc) were determined through Week 52 (nonresponder imputation for treatment failure through Week 24 and for missing data through Week 52). ACR50, tender/swollen joints, low disease activity (LDA) as assessed by composite indices, and radiographic progression (DISCOVER‐2 only) were assessed in patients with dactylitis versus without dactylitis resolution at Week 24 and Week 52.ResultsPatients with dactylitis at baseline (473 of 1118) had more severe joint and skin disease than those without dactylitis (645 of 1118). At Week 52, approximately 75% of guselkumab‐randomized patients with dactylitis at baseline had complete resolution; approximately 80% had at least 70% DSS improvement. Through Week 52, new‐onset dactylitis (DSS ≥1) was uncommon among patients with a DSS of 0 at baseline. Guselkumab‐randomized patients with dactylitis resolution were more likely to achieve ACR50, at least 50% reduction in tender and swollen joints, and LDA at Week 24 and Week 52 than those without resolution. At Week 52, patients with dactylitis resolution had numerically less radiographic progression from baseline (DISCOVER‐2).ConclusionThrough 1 year, approximately 75% of guselkumab‐randomized patients had complete resolution of dactylitis; patients exhibiting resolution were more likely to achieve other important clinical outcomes. Given the high burden of dactylitis, resolution may be associated with better long‐term patient outcomes.

Funder

Janssen Research and Development

Publisher

Wiley

Subject

Rheumatology

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