Effectiveness of secukinumab in radiographic and non-radiographic axial spondyloarthritis: a European routine-care observational study
Jazyk angličtina Země Anglie, Velká Británie Médium electronic
Typ dokumentu časopisecké články, pozorovací studie, multicentrická studie
PubMed
39053949
PubMed Central
PMC11284936
DOI
10.1136/rmdopen-2024-004166
PII: rmdopen-2024-004166
Knihovny.cz E-zdroje
- Klíčová slova
- Epidemiology, Pain, Patient Reported Outcome Measures, Spondylitis, Ankylosing, Therapeutics,
- MeSH
- antirevmatika terapeutické užití MeSH
- axiální spondyloartritida * farmakoterapie etiologie MeSH
- dospělí MeSH
- hodnocení výsledků péče pacientem MeSH
- humanizované monoklonální protilátky * terapeutické užití MeSH
- indukce remise MeSH
- lidé středního věku MeSH
- lidé MeSH
- prospektivní studie MeSH
- rentgendiagnostika MeSH
- stupeň závažnosti nemoci MeSH
- výsledek terapie MeSH
- Check Tag
- dospělí MeSH
- lidé středního věku MeSH
- lidé MeSH
- mužské pohlaví MeSH
- ženské pohlaví MeSH
- Publikační typ
- časopisecké články MeSH
- multicentrická studie MeSH
- pozorovací studie MeSH
- Geografické názvy
- Evropa MeSH
- Názvy látek
- antirevmatika MeSH
- humanizované monoklonální protilátky * MeSH
- secukinumab MeSH Prohlížeč
OBJECTIVES: To compare the treatment effectiveness of secukinumab in radiographic (r) versus non-radiographic (nr) axial spondyloarthritis (axSpA) patients treated in routine care across Europe. METHODS: Prospectively collected data on secukinumab-treated axSpA patients with known radiographic status were pooled from nine countries.Remission rates based on patient-reported outcomes (PROs; Numeric Rating Scale (0-10), for example, pain ≤2/Bath Ankylosing Spondylitis Disease Activity Index (BASDAI) ≤2 and Ankylosing Spondylitis Disease Activity Score (ASDAS) inactive disease (ID) <1.3 after 6/12/24 months of secukinumab treatment were calculated.Remission and drug retention rates in r-axSpA versus nr-axSpA patients were compared by logistic and Cox regression models (unadjusted/adjusted for age+sex/adjusted for multiple confounders). RESULTS: Overall, 1161 secukinumab-treated patients were included (r-axSpA/nr-axSpA: 922/239). At baseline, r-axSpA patients had longer disease duration and higher C reactive protein, were more often male and HLA-B27 positive and had received fewer prior biological or targeted synthetic disease-modifying antirheumatic drugs compared with nr-axSpA patients, whereas PROs were largely similar.During follow-up, crude PRO remission rates were significantly higher in r-axSpA compared with nr-axSpA patients (6 months: pain≤2: 40%/28%, OR=1.7; BASDAI≤2: 37%/25%, OR=1.8), as were drug retention rates (24 months: 66%/58%, HR 0.73 (ref: r-axSpA)). Proportions of patients achieving ASDAS ID were low for both groups, particularly nr-axSpA (6 months: 11%/8%).However, when adjusting for age+sex, these differences diminished, and after adjusting for multiple confounders, no significant between-group differences remained for either remission or drug retention rates. CONCLUSION: Crude remission/drug retention rates in European secukinumab-treated patients were higher in r-axSpA compared with nr-axSpA patients. In adjusted analyses, secukinumab effectiveness was similar in both groups, suggesting that observed differences were related to factors other than radiographic status.
Aberdeen Centre for Arthritis and Musculoskeletal Health University of Aberdeen Aberdeen UK
Amsterdam Rheumatology and Immunology Center Amsterdam Netherlands
Center for treatment of Rheumatic and Musculoskeletal Diseases Diakonhjemmet Hospital Oslo Norway
Clinical Epidemiology Division Department of Medicine Solna Karolinska Institute Stockholm Sweden
Comprehensive Health Research Centre NOVA Medical School Universidade NOVA de Lisboa Lisboa Portugal
Department for Rheumatology Landspitali National University Hospital of Iceland Reykjavik Iceland
Department of Clinical Medicine Aarhus University Aarhus Denmark
Department of Clinical Medicine University of Copenhagen Copenhagen Denmark
Department of Clinical Sciences Lund Lund University Lund Sweden
Department of Medicine Helsinki University and Helsinki University Hospital Helsinki Finland
Department of Rheumatology Aarhus University Hospital Aarhus Denmark
Department of Rheumatology Bakircay Universitesi Izmir Turkey
Department of Rheumatology East Tallinn Central Hospital Tallinn Estonia
Department of Rheumatology Geneva University Hospitals Geneve Switzerland
Department of Rheumatology Hospital Garcia de Orta EPE Almada Portugal
Department of Rheumatology Hospital General Universitario Gregorio Marañón Madrid Spain
Department of Rheumatology Skåne University Hospital Lund Lund Sweden
Department of Rheumatology University Hospital Zurich Zurich Switzerland
Department of Rheumatology University Medical Centre Ljubljana Ljubljana Slovenia
Division of Rheumatology Dokuz Eylul Universitesi Tip Fakultesi Izmir Turkey
Faculty of Medicine Complutense University of Madrid Madrid Spain
Faculty of Medicine University of Iceland Reykjavik Iceland
Faculty of Medicine University of Ljubljana Ljubljana Slovenia
Faculty of Medicine University of Oslo Oslo Norway
Inflammation Center Rheumatology Helsinki University Central Hospital Helsinki Finland
National Institute for Health Development Tallinn Estonia
Public Health Section Inland Norway University of Applied Sciences Elverum Norway
Research Unit Sørlandet Sykehus HF Kristiansand Norway
Research Unit Spanish Society of Rheumatology Madrid Spain
Rheumatology Allergology and Clinical Immunology University of Rome Tor Vergata Roma Italy
Rheumatology Department Centro Hospitalar do Baixo Vouga EPE Aveiro Portugal
Rheumatology Radboud University Medical Center Nijmegen Netherlands
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