Association of clinical response criteria and disease activity levels with axial spondyloarthritis core domains: results from two phase 3 randomised studies, BE MOBILE 1 and 2

Objective To assess how achievement of increasingly stringent clinical response criteria and disease activity states at week 52 translate into changes in core domains in patients with non-radiographic (nr-) and radiographic (r-) axial spondyloarthritis (axSpA).Methods Patients in BE MOBILE 1 and 2 a...

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Published in:RMD Open
Main Authors: Sofia Ramiro, Atul Deodhar, Philip J Mease, Martin Rudwaleit, Jonathan Kay, Marina Magrey, Victoria Navarro-Compán, Vanessa Taieb, Carmen Fleurinck, Ute Massow, Michael F Mørup, Christine de la Loge
Format: Article
Language:English
Published: BMJ Publishing Group 2024-05-01
Online Access:https://rmdopen.bmj.com/content/10/2/e004040.full
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author Sofia Ramiro
Atul Deodhar
Philip J Mease
Martin Rudwaleit
Jonathan Kay
Marina Magrey
Victoria Navarro-Compán
Vanessa Taieb
Carmen Fleurinck
Ute Massow
Michael F Mørup
Christine de la Loge
author_facet Sofia Ramiro
Atul Deodhar
Philip J Mease
Martin Rudwaleit
Jonathan Kay
Marina Magrey
Victoria Navarro-Compán
Vanessa Taieb
Carmen Fleurinck
Ute Massow
Michael F Mørup
Christine de la Loge
author_sort Sofia Ramiro
collection DOAJ
container_title RMD Open
description Objective To assess how achievement of increasingly stringent clinical response criteria and disease activity states at week 52 translate into changes in core domains in patients with non-radiographic (nr-) and radiographic (r-) axial spondyloarthritis (axSpA).Methods Patients in BE MOBILE 1 and 2 achieving different levels of response or disease activity (Assessment of SpondyloArthritis International Society (ASAS) and Ankylosing Spondylitis Disease Activity Score (ASDAS) response criteria, Bath Ankylosing Spondylitis Disease Activity Index (BASDAI50)) at week 52 were pooled, regardless of treatment arm. Associations between achievement of these endpoints and change from baseline (CfB) in patient-reported outcomes (PROs) measuring core axSpA domains, including pain, fatigue, physical function, overall functioning and health, and work and employment, were assessed.Results Achievement of increasingly stringent clinical efficacy endpoints at week 52 was generally associated with sequentially greater improvements from baseline in all PROs. Patients with nr-axSpA achieving ASAS40 demonstrated greater improvements (CfB) than patients who did not achieve ASAS40 but did achieve ASAS20, in total spinal pain (−5.3 vs −2.8, respectively), Functional Assessment of Chronic Illness-Fatigue subscale (12.7 vs 6.7), Bath Ankylosing Spondylitis Function Index (−3.9 vs −1.8), European Quality of Life 5-Dimension 3-Level Version (0.30 vs 0.16), Work Productivity and Activity Impairment-axSpA presenteeism (−35.4 vs −15.9), overall work impairment (−36.5 vs −12.9), activity impairment (−39.0 vs −21.0) and sleep (9.0 vs 3.9). Results were similar for ASDAS and BASDAI50. Similar amplitudes of improvement were observed between patients with nr-axSpA and r-axSpA.Conclusions Patients treated with bimekizumab across the full axSpA disease spectrum, who achieved increasingly stringent clinical response criteria and lower disease activity at week 52, reported larger improvements in core axSpA domains.
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spelling doaj-art-b0bf5a183aca4f3db52fc23fd3c2cd262025-08-19T23:18:39ZengBMJ Publishing GroupRMD Open2056-59332024-05-0110210.1136/rmdopen-2023-004040Association of clinical response criteria and disease activity levels with axial spondyloarthritis core domains: results from two phase 3 randomised studies, BE MOBILE 1 and 2Sofia Ramiro0Atul Deodhar1Philip J Mease2Martin Rudwaleit3Jonathan Kay4Marina Magrey5Victoria Navarro-Compán6Vanessa Taieb7Carmen Fleurinck8Ute Massow9Michael F Mørup10Christine de la Loge11Department of Rheumatology, Zuyderland Medical Centre Heerlen, Heerlen, NetherlandsDivision of Arthritis & Rheumatic Diseases, Oregon Health & Science University, Portland, Oregon, USADepartment of Rheumatology, Swedish Medical Center, Seattle, Washington, USAKlinikum Bielefeld, University of Bielefeld, Bielefeld, Germany12 Division of Rheumatology, Department of Medicine, University of Massachusetts Medical School, Worcester, Massachusetts, USAUniversity Hospitals, Case Western Reserve University, Cleveland, Ohio, USA1 Department of Rheumatology, La Paz University Hospital, Madrid, SpainUCB Pharma, Colombes, FranceUCB Pharma, Brussels, BelgiumUCB Pharma, Monheim am Rhein, Germany10 UCB Pharma, Copenhagen, Denmark7 PCOM Analytics, Avallon, FranceObjective To assess how achievement of increasingly stringent clinical response criteria and disease activity states at week 52 translate into changes in core domains in patients with non-radiographic (nr-) and radiographic (r-) axial spondyloarthritis (axSpA).Methods Patients in BE MOBILE 1 and 2 achieving different levels of response or disease activity (Assessment of SpondyloArthritis International Society (ASAS) and Ankylosing Spondylitis Disease Activity Score (ASDAS) response criteria, Bath Ankylosing Spondylitis Disease Activity Index (BASDAI50)) at week 52 were pooled, regardless of treatment arm. Associations between achievement of these endpoints and change from baseline (CfB) in patient-reported outcomes (PROs) measuring core axSpA domains, including pain, fatigue, physical function, overall functioning and health, and work and employment, were assessed.Results Achievement of increasingly stringent clinical efficacy endpoints at week 52 was generally associated with sequentially greater improvements from baseline in all PROs. Patients with nr-axSpA achieving ASAS40 demonstrated greater improvements (CfB) than patients who did not achieve ASAS40 but did achieve ASAS20, in total spinal pain (−5.3 vs −2.8, respectively), Functional Assessment of Chronic Illness-Fatigue subscale (12.7 vs 6.7), Bath Ankylosing Spondylitis Function Index (−3.9 vs −1.8), European Quality of Life 5-Dimension 3-Level Version (0.30 vs 0.16), Work Productivity and Activity Impairment-axSpA presenteeism (−35.4 vs −15.9), overall work impairment (−36.5 vs −12.9), activity impairment (−39.0 vs −21.0) and sleep (9.0 vs 3.9). Results were similar for ASDAS and BASDAI50. Similar amplitudes of improvement were observed between patients with nr-axSpA and r-axSpA.Conclusions Patients treated with bimekizumab across the full axSpA disease spectrum, who achieved increasingly stringent clinical response criteria and lower disease activity at week 52, reported larger improvements in core axSpA domains.https://rmdopen.bmj.com/content/10/2/e004040.full
spellingShingle Sofia Ramiro
Atul Deodhar
Philip J Mease
Martin Rudwaleit
Jonathan Kay
Marina Magrey
Victoria Navarro-Compán
Vanessa Taieb
Carmen Fleurinck
Ute Massow
Michael F Mørup
Christine de la Loge
Association of clinical response criteria and disease activity levels with axial spondyloarthritis core domains: results from two phase 3 randomised studies, BE MOBILE 1 and 2
title Association of clinical response criteria and disease activity levels with axial spondyloarthritis core domains: results from two phase 3 randomised studies, BE MOBILE 1 and 2
title_full Association of clinical response criteria and disease activity levels with axial spondyloarthritis core domains: results from two phase 3 randomised studies, BE MOBILE 1 and 2
title_fullStr Association of clinical response criteria and disease activity levels with axial spondyloarthritis core domains: results from two phase 3 randomised studies, BE MOBILE 1 and 2
title_full_unstemmed Association of clinical response criteria and disease activity levels with axial spondyloarthritis core domains: results from two phase 3 randomised studies, BE MOBILE 1 and 2
title_short Association of clinical response criteria and disease activity levels with axial spondyloarthritis core domains: results from two phase 3 randomised studies, BE MOBILE 1 and 2
title_sort association of clinical response criteria and disease activity levels with axial spondyloarthritis core domains results from two phase 3 randomised studies be mobile 1 and 2
url https://rmdopen.bmj.com/content/10/2/e004040.full
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