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Certolizumab Pegol Efficacy in Patients With Non-Radiographic Axial Spondyloarthritis Stratified by Baseline MRI and C-Reactive Protein Status: An Analysis From the C-axSpAnd Study.
Robinson, Philip C; Maksymowych, Walter P; Gensler, Lianne S; Hall, Stephen; Rudwaleit, Martin; Hoepken, Bengt; Bauer, Lars; Kumke, Thomas; Kim, Mindy; de Peyrecave, Natasha; Deodhar, Atul.
Afiliação
  • Robinson PC; University of Queensland School of Clinical Medicine, Brisbane, Queensland, Australia.
  • Maksymowych WP; University of Alberta, Edmonton, Canada.
  • Gensler LS; University of California San Francisco.
  • Hall S; Monash University and Emeritus Research, Melbourne, Victoria, Australia.
  • Rudwaleit M; University of Bielefeld, Bielefeld, Germany.
  • Hoepken B; UCB Pharma, Monheim am Rhein, Germany.
  • Bauer L; UCB Pharma, Monheim am Rhein, Germany.
  • Kumke T; UCB Pharma, Monheim am Rhein, Germany.
  • Kim M; UCB Pharma, Raleigh, North Carolina.
  • de Peyrecave N; UCB Pharma, Brussels, Belgium.
  • Deodhar A; Oregon Health & Science University, Portland.
ACR Open Rheumatol ; 4(9): 794-801, 2022 Sep.
Article em En | MEDLINE | ID: mdl-35733363
ABSTRACT

OBJECTIVE:

Tumor necrosis factor inhibitors (TNFi) are an effective treatment for non-radiographic axial spondyloarthritis (nr-axSpA). To be eligible, however, many authorities require patients with nr-axSpA to show active sacroiliitis on magnetic resonance imaging (MRI) and/or an elevated C-reactive protein (CRP) level, possibly resulting in a perception that patients with nr-axSpA without both factors have only low responses to TNFi treatment. We evaluated clinical responses to certolizumab pegol (CZP) in patients with nr-axSpA stratified by baseline MRI/CRP status.

METHODS:

C-axSpAnd was a phase 3, multicenter study on CZP in adult patients with active nr-axSpA and objective signs of inflammation. This analysis assessed efficacy of CZP over the 52-week randomized, double-blind, placebo-controlled period in patients stratified into subgroups based on the presence of active sacroiliitis on MRI and CRP level at baseline.

RESULTS:

CZP-treated patients across all MRI/CRP subgroups achieved clinical responses greater than placebo. Across outcome measures, CZP-treated MRI+/CRP+ patients demonstrated the greatest clinical responses, but substantial improvements were also observed in CZP-treated MRI+/CRP- and MRI-/CRP+ patients. Ankylosing Spondylitis Disease Activity Score Major Improvement response rates at week 52 among CZP-treated patients (75.6% MRI+/CRP+; 47.5% MRI-/CRP+; and 29.7% MRI+/CRP-) were higher than rates in placebo groups (range 3.9%-12.5%). Assessment of SpondyloArthritis international Society 40% response, Bath Ankylosing Spondylitis Disease Activity Index, and Bath Ankylosing Spondyloarthritis Functional Index had similar response patterns, although differences between the CZP-treated MRI/CRP subgroups were smaller. Clinical responses among CZP-treated patients were also observed in additional subgroups, including those with low Spondyloarthritis Research Consortium of Canada MRI sacroiliac joint inflammation scores and those with normal baseline CRP levels.

CONCLUSION:

Our findings indicate that CZP treatment benefits patients with nr-axSpA across MRI+/CRP+, MRI-/CRP+, and MRI+/CRP- subgroups.

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Tipo de estudo: Clinical_trials Idioma: En Revista: ACR Open Rheumatol Ano de publicação: 2022 Tipo de documento: Article País de afiliação: Austrália

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Tipo de estudo: Clinical_trials Idioma: En Revista: ACR Open Rheumatol Ano de publicação: 2022 Tipo de documento: Article País de afiliação: Austrália