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The impact of seropositivity on the effectiveness of biologic anti-rheumatic agents: results from a collaboration of 16 registries
DS. Courvoisier, K. Chatzidionysiou, D. Mongin, K. Lauper, X. Mariette, J. Morel, JE. Gottenberg, SA. Bergstra, MP. Suarez, C. Codreanu, TK. Kvien, MJ. Santos, K. Pavelka, ML. Hetland, J. Askling, C. Turesson, S. Kubo, Y. Tanaka, F. Iannone, D....
Language English Country Great Britain
Document type Journal Article, Observational Study
NLK
Free Medical Journals
from 1996 to 1 year ago
Open Access Digital Library
from 1996-01-01
Medline Complete (EBSCOhost)
from 1999-01-01 to 1 year ago
- MeSH
- Antirheumatic Agents * classification immunology therapeutic use MeSH
- Biological Products * classification immunology therapeutic use MeSH
- Drug Interactions immunology MeSH
- Middle Aged MeSH
- Humans MeSH
- International Cooperation MeSH
- Monitoring, Immunologic * methods statistics & numerical data MeSH
- Withholding Treatment statistics & numerical data MeSH
- Patient Acuity MeSH
- Registries statistics & numerical data MeSH
- Arthritis, Rheumatoid * diagnosis drug therapy epidemiology immunology MeSH
- Rheumatoid Factor blood MeSH
- Duration of Therapy MeSH
- Patient Selection MeSH
- Treatment Outcome MeSH
- Check Tag
- Middle Aged MeSH
- Humans MeSH
- Male MeSH
- Female MeSH
- Publication type
- Journal Article MeSH
- Observational Study MeSH
OBJECTIVES: RF and ACPA are used as diagnostic tools and their presence has been associated with clinical response to some biologic DMARDs (bDMARDs) in RA. This study compared the impact of seropositivity on drug discontinuation and effectiveness of bDMARDs in patients with RA, using head-to-head comparisons in a real-world setting. METHODS: We conducted a pooled analysis of 16 observational RA registries. Inclusion criteria were a diagnosis of RA, initiation of treatment with rituximab (RTX), abatacept (ABA), tocilizumab (TCZ) or TNF inhibitors (TNFis) and available information on RF and/or ACPA status. Drug discontinuation was analysed using Cox regression, including drug, seropositivity, their interaction, adjusting for concomitant and past treatments and patient and disease characteristics and accounting for country and calendar year of bDMARD initiation. Effectiveness was analysed using the Clinical Disease Activity Index evolution over time. RESULTS: Among the 27 583 eligible patients, the association of seropositivity with drug discontinuation differed across bDMARDs (P for interaction <0.001). The adjusted hazard ratios for seropositive compared with seronegative patients were 1.01 (95% CI 0.95, 1.07) for TNFis, 0.89 (0.78, 1.02)] for TCZ, 0.80 (0.72, 0.88) for ABA and 0.70 (0.59, 0.84) for RTX. Adjusted differences in remission and low disease activity rates between seropositive and seronegative patients followed the same pattern, with no difference in TNFis, a small difference in TCZ, a larger difference in ABA and the largest difference in RTX (Lundex remission difference +5.9%, low disease activity difference +11.6%). CONCLUSION: Seropositivity was associated with increased effectiveness of non-TNFi bDMARDs, especially RTX and ABA, but not TNFis.
Center of Rheumatic Diseases University of Medicine and Pharmacy Bucharest Romania
Clinical Epidemiology Karolinska Institutet Stockholm Sweden
Clinical Medicine University of Copenhagen Copenhagen Denmark
DANBIO Registry and Copenhagen Center for Arthritis Research Rigshospitalet Glostrup Denmark
Italian Group for the Study of Early Arthritis University Hospital of Bari Bari Italy
Rheumatology 5 A Nasonova Research Institute of Rheumatology Moscow Russia
Rheumatology and Clinical Immunology Amsterdam University Medical Centers Amsterdam The Netherlands
Rheumatology Charles University Prague Czech Republic
Rheumatology CHU and University of Montpellier Montpellier France
Rheumatology Clinical University Hospital Santiago de Compostela Spain
Rheumatology Diakonhjemmet Hospital Oslo Norway
Rheumatology Hospital Garcia de Orta Almada Portugal
Rheumatology Karolinska Institutet Stockholm Sweden
Rheumatology Leiden University Medical Center Leiden The Netherlands
Rheumatology Skåne University Hospital Malmö Sweden
Rheumatology Université Paris Sud AP HP Paris France
Rheumatology University Hospital of Strasbourg Strasbourg France
Rheumatology University Hospitals of Geneva Geneva Switzerland
Rheumatology University Medical Centre Ljubljana Ljubljana Slovenia
ROB FIN Registry Helsinki University Hospital and Helsinki University Helsinki Finland
References provided by Crossref.org
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