Impact of Ixekizumab on Work Productivity in Patients with Ankylosing Spondylitis: Results from the COAST-V and COAST-W Trials at 52 Weeks.

Ankylosing spondylitis Axial spondyloarthritis Ixekizumab Radiographic axial spondyloarthritis Work productivity

Journal

Rheumatology and therapy
ISSN: 2198-6576
Titre abrégé: Rheumatol Ther
Pays: England
ID NLM: 101674543

Informations de publication

Date de publication:
Dec 2020
Historique:
received: 29 05 2020
pubmed: 21 8 2020
medline: 21 8 2020
entrez: 21 8 2020
Statut: ppublish

Résumé

Patients with ankylosing spondylitis (AS) are burdened with symptoms impacting work productivity measured by presenteeism, absenteeism, overall work impairment, and activity impairment. Ixekizumab, a high-affinity monoclonal antibody selectively targeting interleukin-17A, has been demonstrated to improve disease signs and symptoms in two phase 3 trials of AS. This study investigated for 52 weeks the effect of ixekizumab treatment on work productivity in patients with active AS. COAST-V (NCT02696785) and COAST-W (NCT02696798) were phase 3, multicenter, randomized, controlled trials investigating the efficacy of ixekizumab 80 mg every 4 weeks (Q4W) and every 2 weeks (Q2W) in patients with AS naïve to biologic disease-modifying antirheumatic drugs (bDMARDs; COAST-V) or who were inadequate responders or intolerant to tumor necrosis factor inhibitors (TNFi; COAST-W). Work productivity was measured with the Work Productivity and Activity Impairment Questionnaire for Spondyloarthritis at weeks 16 and 52. Absenteeism, presenteeism, and overall work impairment were assessed for patients reporting paid work. Activity impairment was assessed regardless of work status. At baseline, 66.2% (434/656) of patients reported paid work. At week 16, bDMARD-naïve patients treated with both ixekizumab dose regimens and TNFi-experienced patients treated with ixekizumab Q2W reported significant improvements in activity impairment (p < 0.01 and p < 0.05, respectively). TNFi-experienced patients treated with ixekizumab showed significant improvements versus placebo in presenteeism and overall work impairment (p < 0.05); bDMARD-naïve patients had numeric improvements. After week 16, patients initially on placebo switched to ixekizumab and patients already treated with ixekizumab continued treatment. Improvements in work productivity and daily activity were sustained through week 52 for both bDMARD-experienced and -naïve patients. Both bDMARD-naïve and TNFi-experienced patients with AS had greater improvements in work productivity and activity impairment when receiving ixekizumab compared to placebo at week 16. Improvements in work productivity and activity impairment achieved at week 16 were sustained through week 52 with ixekizumab treatment.

Identifiants

pubmed: 32814997
doi: 10.1007/s40744-020-00225-4
pii: 10.1007/s40744-020-00225-4
pmc: PMC7695773
doi:

Types de publication

Journal Article

Langues

eng

Pagination

759-774

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Auteurs

Helena Marzo-Ortega (H)

National Institute for Health Research-Leeds Biomedical Research Centre (NIHR-LBRC), Leeds Teaching Hospitals Trust and Leeds Institute of Rheumatic and Musculoskeletal Medicine (LIRMM), University of Leeds, Leeds, West Yorkshire, UK. h.marzo-ortega@leeds.ac.uk.

Philip J Mease (PJ)

Swedish Medical Center-Providence St. Joseph Health and University of Washington, Seattle, WA, USA.
University of Washington School of Medicine, Seattle, WA, USA.

Proton Rahman (P)

Memorial University of Newfoundland, St. John's, NL, Canada.

Victoria Navarro-Compán (V)

Hospital Universitario La Paz IdiPaz, Madrid, Spain.

Vibeke Strand (V)

Division Immunology/Rheumatology, Stanford University School of Medicine, Palo Alto, CA, USA.

Maxime Dougados (M)

Department of Rheumatology, Cochin Hospital, Paris, France.

Bernard Combe (B)

Department of Rheumatology, CHU Montpellier and Montpellier University, Montpellier, France.

James Cheng-Chung Wei (JC)

Graduate Institute of Integrated Medicine, Chung Shan Medical University, China Medical University, Taichung City, Taiwan.

Xenofon Baraliakos (X)

St. Elisabeth Group GmbH, Herne, Germany.

Theresa Hunter (T)

Eli Lilly and Company, Indianapolis, IN, USA.

David Sandoval (D)

Eli Lilly and Company, Indianapolis, IN, USA.

Xiaoqi Li (X)

Eli Lilly and Company, Indianapolis, IN, USA.

Baojin Zhu (B)

Eli Lilly and Company, Indianapolis, IN, USA.

Louis Bessette (L)

Centre hospitalier universitaire de Québec-Laval University, Quebec City, QC, Canada.

Atul Deodhar (A)

Division of Arthritis and Rheumatic Diseases, Oregon Health and Science University, Portland, OR, USA.

Classifications MeSH