dc.contributor.author | Ørnbjerg L.M. | |
dc.contributor.author | Rugbjerg K. | |
dc.contributor.author | Georgiadis S. | |
dc.contributor.author | Rasmussen S.H. | |
dc.contributor.author | Lindström U. | |
dc.contributor.author | Pavelka K. | |
dc.contributor.author | Yilmaz N. | |
dc.date.accessioned | 2024-02-04T13:30:21Z | |
dc.date.available | 2024-02-04T13:30:21Z | |
dc.date.issued | 2023 | |
dc.identifier.issn | 0315162X | |
dc.identifier.uri | https://doi.org/10.3899/jrheum.220459 | |
dc.identifier.uri | http://hdl.handle.net/11446/4899 | |
dc.description.abstract | Objective. To investigate the distribution of patient-reported outcomes (PROs) in patients with axial spondyloarthritis (axSpA) initiating a tumor necrosis factor inhibitor (TNFi), to assess the proportion reaching PRO “remission” across registries and treatment series, and to compare patients registered to fulfill the modified New York (mNY) criteria for ankylosing spondylitis (AS) vs patients with nonradiographic axSpA (nr-axSpA). Methods. Fifteen European registries contributed PRO scores for pain, fatigue, patient global assessment (PtGA), Bath Ankylosing Spondylitis (AS) Disease Activity Index (BASDAI), Bath AS Functional Index (BASFI), and Health Assessment Questionnaire (HAQ) from 19,498 patients with axSpA. Changes in PROs and PRO remission rates (definitions: ? 20 mm for pain, fatigue, PtGA, BASDAI, and BASFI; ? 0.5 for HAQ) were calculated at 6, 12, and 24 months of treatment. Results. Heterogeneity in baseline characteristics and outcomes between registries were observed. In pooled data, 6 months after the start of a first TNFi, pain score was reduced by approximately 60% (median at baseline/6/12/24 months: 65/25/20/20 mm) in patients on treatment. Similar patterns were observed for fatigue (68/32/30/25 mm), PtGA (66/29/21/20 mm), BASDAI (58/26/21/19 mm), BASFI (46/20/16/16 mm), and HAQ (0.8/0.4/0.2/0.2). Patients with AS (n = 3281) had a slightly better response than patients with nr-axSpA (n = 993). The Lund Efficacy Index (LUNDEX)-adjusted remission rates at 6 months for pain/fatigue/PtGA/BASDAI/BASFI/HAQ were 39%/30%/38%/34%/35%/48% for the AS cohort and 30%/21%/26%/24%/33%/47% for the nr-axSpA cohort. Better PRO responses were seen with a first TNFi compared to a second and third TNFi. Conclusion. Patients with axSpA starting a TNFi achieved high PRO remission rates, most pronounced in those fulfilling the mNY criteria and for the first TNFi. © 2023 The Journal of Rheumatology. | en_US |
dc.description.sponsorship | Novartis | en_US |
dc.description.sponsorship | On behalf of the EuroSpA Scientific Committee, the authors acknowledge Novartis Pharma AG and IQVIA for supporting the EuroSpA collaboration. | en_US |
dc.description.sponsorship | The European Spondyloarthritis Research Collaboration Network was financially supported by Novartis Pharma AG. Novartis had no influence on the data collection, statistical analyses, manuscript preparation, or decision to submit the manuscript. 1L.M. Ørnbjerg, MD, PhD, K. Rugbjerg, MSc, PhD, S. Georgiadis, PhD, S.H. Rasmussen, PhD, Copenhagen Center for Arthritis Research (COPECARE), Centre for Rheumatology and Spine Diseases, Centre of Head and Orthopaedics, Copenhagen University Hospital, Glostrup, Denmark; 2U. Lindström, MD, PhD, Department of Rheumatology and Inflammation Research, University of Gothenburg Sahlgrenska Academy, Gothenburg, Sweden; 3K. Pavelka, MD, PhD, Institute of Rheumatology, and Department of Rheumatology, First Faculty of Medicine, Charles | en_US |
dc.language.iso | eng | en_US |
dc.publisher | Journal of Rheumatology | en_US |
dc.relation.ispartof | Journal of Rheumatology | en_US |
dc.identifier.doi | 10.3899/jrheum.220459 | |
dc.rights | info:eu-repo/semantics/closedAccess | en_US |
dc.subject | axial spondyloarthritis | en_US |
dc.subject | patient-reported outcome measures | en_US |
dc.subject | tumor necrosis factor inhibitors | en_US |
dc.subject | adalimumab | en_US |
dc.subject | certolizumab pegol | en_US |
dc.subject | etanercept | en_US |
dc.subject | golimumab | en_US |
dc.subject | infliximab | en_US |
dc.subject | tumor necrosis factor inhibitor | en_US |
dc.subject | tumor necrosis factor | en_US |
dc.subject | tumor necrosis factor inhibitor | en_US |
dc.subject | adult | en_US |
dc.subject | Article | en_US |
dc.subject | axial spondyloarthritis | en_US |
dc.subject | Bath ankylosing spondylitis disease activity index | en_US |
dc.subject | Bath ankylosing spondylitis functional index | en_US |
dc.subject | clinical outcome | en_US |
dc.subject | Europe | en_US |
dc.subject | fatigue | en_US |
dc.subject | female | en_US |
dc.subject | Health Assessment Questionnaire | en_US |
dc.subject | human | en_US |
dc.subject | major clinical study | en_US |
dc.subject | male | en_US |
dc.subject | non-radiographic axial spondyloarthritis | en_US |
dc.subject | pain | en_US |
dc.subject | pain assessment | en_US |
dc.subject | patient-reported outcome | en_US |
dc.subject | remission | en_US |
dc.subject | treatment response | en_US |
dc.subject | ankylosing spondylitis | en_US |
dc.subject | fatigue | en_US |
dc.subject | non-radiographic axial spondyloarthritis | en_US |
dc.subject | pain | en_US |
dc.subject | spondylarthritis | en_US |
dc.subject | treatment outcome | en_US |
dc.subject | Fatigue | en_US |
dc.subject | Humans | en_US |
dc.subject | Non-Radiographic Axial Spondyloarthritis | en_US |
dc.subject | Pain | en_US |
dc.subject | Spondylarthritis | en_US |
dc.subject | Spondylitis, Ankylosing | en_US |
dc.subject | Treatment Outcome | en_US |
dc.subject | Tumor Necrosis Factor Inhibitors | en_US |
dc.subject | Tumor Necrosis Factor-alpha | en_US |
dc.title | One-Third of European Patients With Axial Spondyloarthritis Reach Pain Remission With Routine Care Tumor Necrosis Factor Inhibitor Treatment | en_US |
dc.type | article | en_US |
dc.department | DBÜ | en_US |
dc.identifier.issue | 8 | en_US |
dc.identifier.volume | 50 | en_US |
dc.identifier.startpage | 1009 | en_US |
dc.identifier.endpage | 1019 | en_US |
dc.relation.publicationcategory | Makale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanı | en_US |
dc.department-temp | Ørnbjerg, L.M., Copenhagen Center for Arthritis Research (COPECARE), Centre for Rheumatology and Spine Diseases, Centre of Head and Orthopaedics, Copenhagen University Hospital, Glostrup, Denmark; Rugbjerg, K., Copenhagen Center for Arthritis Research (COPECARE), Centre for Rheumatology and Spine Diseases, Centre of Head and Orthopaedics, Copenhagen University Hospital, Glostrup, Denmark; Georgiadis, S., Copenhagen Center for Arthritis Research (COPECARE), Centre for Rheumatology and Spine Diseases, Centre of Head and Orthopaedics, Copenhagen University Hospital, Glostrup, Denmark; Rasmussen, S.H., Copenhagen Center for Arthritis Research (COPECARE), Centre for Rheumatology and Spine Diseases, Centre of Head and Orthopaedics, Copenhagen University Hospital, Glostrup, Denmark; Lindström, U., Department of Rheumatology and Inflammation Research, University of Gothenburg Sahlgrenska Academy, Gothenburg, Sweden; Pavelka, K., Institute of Rheumatology, Department of Rheumatology, First Faculty of Medicine, Charles University, Prague, Czech Republic; Yilmaz, N., Department of Rheumatology, Demiroglu Bilim University, Istanbul, Turkey; Favalli, E.G., Division of Clinical Rheumatology, ASST Gaetano Pini-CTO Institute, Milan, Italy; Nissen, M.J., Department of Rheumatology, Geneva University Hospital, Geneva, Switzerland; Michelsen, B., | en_US |
dc.identifier.pmid | 36455943 | en_US |
dc.identifier.scopus | 2-s2.0-85166052278 | en_US |
dc.authorscopusid | 24069275900 | |
dc.authorscopusid | 24475168600 | |
dc.authorscopusid | 55453151500 | |
dc.authorscopusid | 57844942500 | |
dc.authorscopusid | 56624176500 | |
dc.authorscopusid | 57209490653 | |
dc.authorscopusid | 35489690300 | |