A Fifty-Two-Week, Randomized, Placebo-Controlled Trial of Certolizumab Pegol in Nonradiographic Axial Spondyloarthritis.


Journal

Arthritis & rheumatology (Hoboken, N.J.)
ISSN: 2326-5205
Titre abrégé: Arthritis Rheumatol
Pays: United States
ID NLM: 101623795

Informations de publication

Date de publication:
07 2019
Historique:
received: 21 11 2018
accepted: 19 02 2019
pubmed: 9 3 2019
medline: 7 1 2020
entrez: 9 3 2019
Statut: ppublish

Résumé

The natural history of nonradiographic axial spondyloarthritis (SpA) is incompletely characterized, and there are concerns that nonsteroidal antiinflammatory drugs provide inadequate disease control in patients with active disease. This study was undertaken to investigate the effects of certolizumab pegol (CZP), an anti-tumor necrosis factor treatment, in patients with nonradiographic axial SpA with objective signs of inflammation. In this ongoing parallel-group double-blind study, adults with active disease were recruited from 80 centers in Australia, Europe, North America, and Taiwan, and were randomized 1:1 to receive placebo or CZP (400 mg at weeks 0, 2, and 4, followed by 200 mg every 2 weeks) in addition to nonbiologic background medication (NBBM). Switching to open-label CZP (or other biologic) or making background medication changes was permitted at any point during the trial, although changes before week 12 were discouraged. The primary end point was the proportion of patients achieving major improvement (MI) (i.e., a ≥2.0-point decrease in the score from baseline or achievement of the lowest possible score [0.6]) in the Ankylosing Spondylitis Disease Activity Score (ASDAS) at week 52. A total of 317 patients were randomized to receive placebo plus NBBM (n = 158) or CZP plus NBBM (n = 159). ASDAS-MI at week 52 was achieved in 47.2% (75 of 159) of CZP plus NBBM patients, which was significantly greater (P < 0.0001) than the 7.0% (11 of 158) of placebo plus NBBM patients in whom ASDAS-MI was achieved. Of the placebo plus NBBM patients, 60.8% (96 of 158) switched to open-label treatment before week 52 compared to 12.6% (20 of 159) of the CZP plus NBBM patients. Adding CZP to background medication is superior to adding placebo in patients with active nonradiographic axial SpA. These results indicate that remission in nonradiographic axial SpA treated without biologics occurs infrequently, demonstrating the need for treatment beyond nonbiologic therapy.

Identifiants

pubmed: 30848558
doi: 10.1002/art.40866
pmc: PMC6619287
doi:

Substances chimiques

Tumor Necrosis Factor Inhibitors 0
C-Reactive Protein 9007-41-4
Certolizumab Pegol UMD07X179E

Banques de données

ClinicalTrials.gov
['NCT02552212']

Types de publication

Journal Article Randomized Controlled Trial Research Support, Non-U.S. Gov't Video-Audio Media

Langues

eng

Sous-ensembles de citation

IM

Pagination

1101-1111

Informations de copyright

© 2019 The Authors. Arthritis & Rheumatology published by Wiley Periodicals, Inc. on behalf of American College of Rheumatology.

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Auteurs

Atul Deodhar (A)

Oregon Health & Science University, Portland.

Lianne S Gensler (LS)

University of California, San Francisco.

Jonathan Kay (J)

UMass Memorial Medical Center and University of Massachusetts Medical School, Worcester.

Walter P Maksymowych (WP)

University of Alberta, Edmonton, Alberta, Canada.

Nigil Haroon (N)

University Health Network and University of Toronto, Toronto, Ontario, Canada.

Robert Landewé (R)

Academic Medical Center and Zuyderland Medical Center, Heerlen, The Netherlands.

Martin Rudwaleit (M)

Klinikum Bielefeld, Bielefeld, Germany.

Stephen Hall (S)

Cabrini Medical Centre, Monash University, and Emeritus Research, Melbourne, Victoria, Australia.

Lars Bauer (L)

UCB Pharma, Monheim am Rhein, Germany.

Bengt Hoepken (B)

UCB Pharma, Monheim am Rhein, Germany.

Natasha de Peyrecave (N)

UCB Pharma, Brussels, Belgium.

Brian Kilgallen (B)

UCB Pharma, Raleigh, North Carolina.

Désirée van der Heijde (D)

Leiden University Medical Center, Leiden, The Netherlands.

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