Implementation of the OMERACT Psoriatic Arthritis Magnetic Resonance Imaging Scoring System in a randomized phase IIb study of abatacept in psoriatic arthritis

Author:

Østergaard Mikkel12ORCID,Bird Paul3,Pachai Chahin4,Du Shuyan4,Wu Chun5,Landis Jessica5,Fuerst Thomas6,Ahmad Harris A7ORCID,Connolly Sean E8,Conaghan Philip G910

Affiliation:

1. Copenhagen Center for Arthritis Research, Center for Rheumatology and Spine Diseases, Copenhagen University Hospital Rigshospitalet , Glostrup

2. Department of Clinical Medicine, University of Copenhagen , Copenhagen, Denmark

3. Division of Medicine, University of New South Wales , Sydney, NSW, Australia

4. Translational Medicine

5. Translational Bioinformatics, Bristol Myers Squibb , Princeton, NJ

6. Medical and Scientific Affairs, Bioclinica Inc. , Newark, CA

7. Medical Affairs, Immunology and Fibrosis

8. Global Drug Development, Bristol Myers Squibb , Princeton, NJ, USA

9. Leeds Institute of Rheumatic and Musculoskeletal Medicine, University of Leeds

10. NIHR Leeds Biomedical Research Centre , Leeds, UK

Abstract

Abstract Objectives To investigate if the OMERACT PsA MRI Scoring System (PsAMRIS), including a novel total inflammation score, shows sensitivity to change with an agent (abatacept) known to impact clinical outcomes in PsA. Methods We performed a post hoc analysis of a randomized phase IIb study of abatacept in patients with PsA and inadequate DMARD response. Participants received one of three abatacept dosing regimens [ABA3, ABA10 or ABA30/10 mg/kg (30 mg/kg switched to 10 mg/kg after two doses)] or placebo until day 169, then ABA10 through day 365. MRIs at baseline and days 85, 169 and 365 were centrally evaluated by two readers blinded to chronological order and treatment arm. Synovitis, osteitis, tenosynovitis, periarticular inflammation, bone erosions, joint space narrowing and bone proliferation were assessed using the PsAMRIS. A novel total inflammation score was tested. Results MRIs for 123 patients were included. On day 169, ABA10 and ABA30/10 significantly reduced MRI synovitis and tenosynovitis, respectively, vs placebo [differences −0.966 (P = 0.039) and −1.652 (P = 0.014), respectively]. Synovitis in the placebo group increased non-significantly from baseline to day 169, total inflammation and tenosynovitis decreased non-significantly and all measures improved significantly after a switch to ABA10 [−1.019, −0.940, −2.275 (P < 0.05), respectively, day 365 vs day 169]. Structural outcomes changed minimally across groups. Conclusion Adults with PsA receiving ABA10 and ABA30/10 demonstrated significant resolution of inflammatory components of disease, confirmed by MRI, with synovitis and tenosynovitis improvements consistent with previously reported clinical responses for these doses. Results indicate that a reduction in OMERACT PsAMRIS inflammation scores may provide proof of tissue-level efficacy in PsA clinical trials. Registration ClinicalTrials.gov (https://clinicaltrials.gov), NCT00534313.

Funder

Bristol Myers Squibb

Publisher

Oxford University Press (OUP)

Subject

Pharmacology (medical),Rheumatology

Reference21 articles.

1. Psoriatic arthritis: epidemiology, clinical features, course, and outcome;Gladman;Ann Rheum Dis,2005

2. Prevalence of rheumatologist-diagnosed psoriatic arthritis in patients with psoriasis in European/North American dermatology clinics;Mease;J Am Acad Dermatol,2013

3. Efficacy and safety of abatacept, a T-cell modulator, in a randomised, double-blind, placebo-controlled, phase III study in psoriatic arthritis;Mease;Ann Rheum Dis,2017

4. Abatacept for the treatment of adults with psoriatic arthritis: patient selection and perspectives;Noisette;Psoriasis (Auckl),2018

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