Evidence map›Paper›PMID 32814997›Full record

ArticleRheumatology and therapy2020

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

Helena Marzo-Ortega, Philip J Mease, Proton Rahman, Victoria Navarro-Compán, Vibeke Strand, Maxime Dougados, Bernard Combe, James Cheng-Chung Wei, Xenofon Baraliakos, Theresa Hunter and 5 more

2 registry-linked trialsOpen access · goldAbstract read
In one paragraph

Article in Rheumatology and therapy, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to 2 registered trials, which are not on this map. Cited by 5 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed, 1 pooled it
1.2field-weighted citation impact, top 20% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

NCT02696785 phase3completednot on this map

A Multicenter, Randomized, Double-Blind, Active and Placebo-Controlled 16-Week Study Followed by Long-Term Evaluation of Efficacy and Safety of Ixekizumab (LY2439821) in bDMARD-Naive Patients With Radiographic Axial Spondyloarthritis

TypeinterventionalSponsorEli Lilly and CompanyRan2016 to 2018Enrolled341ConditionsSpondyloarthritisArmsIxekizumab, Placebo, Adalimumab
NCT02696798 phase3completednot on this map

A Multicenter, Randomized, Double-Blind, Placebo- Controlled 16-Week Study Followed by Long-Term Evaluation of Efficacy and Safety of Ixekizumab (LY2439821) in TNFi-Experienced Patients With Radiographic Axial Spondyloarthritis

TypeinterventionalSponsorEli Lilly and CompanyRan2016 to 2019Enrolled316ConditionsSpondyloarthritisArmsIxekizumab, Placebo
3 · Its place in the literature

Who cites it

5 citing papers in PubMed, 1 synthesis or guideline pooled it, 8 citations in OpenAlex.

  1. Pooled it
  2. Review
  3. Review
  4. Article
  5. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

15 authors at 11 institutions in 6 countries.

Helena Marzo-OrtegaNational 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.ORCID http://orcid.org/0000-0002-9683-3407
Philip J MeaseSwedish Medical Center-Providence St. Joseph Health and University of Washington, Seattle, WA, USA.
Proton RahmanMemorial University of Newfoundland, St. John's, NL, Canada.
Victoria Navarro-CompánHospital Universitario La Paz IdiPaz, Madrid, Spain.
Vibeke StrandDivision Immunology/Rheumatology, Stanford University School of Medicine, Palo Alto, CA, USA.
Maxime DougadosDepartment of Rheumatology, Cochin Hospital, Paris, France.
Bernard CombeDepartment of Rheumatology, CHU Montpellier and Montpellier University, Montpellier, France.
James Cheng-Chung WeiGraduate Institute of Integrated Medicine, Chung Shan Medical University, China Medical University, Taichung City, Taiwan.
Xenofon BaraliakosSt. Elisabeth Group GmbH, Herne, Germany.
Theresa HunterEli Lilly and Company, Indianapolis, IN, USA.
David SandovalEli Lilly and Company, Indianapolis, IN, USA.
Xiaoqi LiEli Lilly and Company, Indianapolis, IN, USA.
Baojin ZhuEli Lilly and Company, Indianapolis, IN, USA.
Louis BessetteCentre hospitalier universitaire de Québec-Laval University, Quebec City, QC, Canada.
Atul DeodharDivision of Arthritis and Rheumatic Diseases, Oregon Health and Science University, Portland, OR, USA.
Eli Lilly (United States) · USCentre hospitalier universitaire de Québec · CAChina Medical University · TWHôpital Cochin · FRHospital Universitario La Paz · ESMemorial University of Newfoundland · CAOregon Health & Science University · USProvidence College · USStanford University · USUniversité de Montpellier · FRUniversity of Leeds · GB

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

introductionPatients 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.

methodsCOAST-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.

resultsAt 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.

conclusionBoth 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.

Indexed as

Ankylosing spondylitisAxial spondyloarthritisIxekizumabRadiographic axial spondyloarthritisWork productivity

Identifiers

PMID32814997
PMCPMC7695773
OpenAlexW3064100784

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
Read underepoch 390

Registered trials

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.