Cardiovascular Risk Factors and the Risk of Discontinuation of Advanced Therapies Due to Treatment Failure in Rheumatoid Arthritis: Results From the Ontario Best Practices Research Initiative
Objectives Our goal was to investigate whether cardiovascular disease (CVD) risk factors are associated with the retention of biologic disease‐modifying antirheumatic drugs (bDMARDs) or targeted‐synthetic DMARDs (tsDMARDs) in patients with rheumatoid arthritis (RA). Methods We included participants...
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Published in | ACR open rheumatology Vol. 5; no. 12; pp. 712 - 717 |
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Main Authors | , , , , |
Format | Journal Article |
Language | English |
Published |
Boston, USA
Wiley Periodicals, Inc
01.12.2023
John Wiley & Sons, Inc Wiley |
Subjects | |
Online Access | Get full text |
ISSN | 2578-5745 2578-5745 |
DOI | 10.1002/acr2.11629 |
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Summary: | Objectives
Our goal was to investigate whether cardiovascular disease (CVD) risk factors are associated with the retention of biologic disease‐modifying antirheumatic drugs (bDMARDs) or targeted‐synthetic DMARDs (tsDMARDs) in patients with rheumatoid arthritis (RA).
Methods
We included participants in the Ontario Best Practices Initiative RA registry who initiated their first bDMARD or tsDMARD. Participants were grouped by the number of baseline CVD risk factors (0, 1, or ≥2). The primary outcome was time‐to‐discontinuation of therapy for any reason. Secondary outcomes included discontinuation for primary failure, secondary failure, or due to adverse events. Competing risks hazards model, adjusted for clinically important confounders, estimated the association between CVD risk factors and treatment retention.
Results
The sample included 872 patients, of which 58% (n = 508) discontinued their b/tsDMARD after a median of 13 months from the time of initiation. The most common causes for treatment discontinuation were primary failure (n = 72), secondary failure (n = 126), or adverse events (n = 133). Patients with no CVD risk factors experienced significantly longer treatment survival compared to patients with 1 or ≥2 CVD risk factors. In multivariable‐adjusted analysis, there was no association between all‐cause discontinuation and CVD risk factors. However, there was a significant association between the presence of >1 CVD risk factor and treatment discontinuation, notably due to secondary treatment failure, but not due to adverse events.
Conclusion
Multiple CVD risk factors increase the risk of treatment failure in RA, particularly for secondary treatment failure. To improve patient outcomes, future research should focus on developing strategies to identify early treatment nonresponse and investigate the potential modifiability of this association. |
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Bibliography: | 1 2 3 https://onlinelibrary.wiley.com/doi/10.1002/acr2.11629 Bindee Kuriya, MD, SM: Sinai Health System, University of Toronto, Toronto, Ontario, Canada. Samar Aboulenain, MBBCh: St. Michael's Hospital, Toronto, Ontario, Canada Author disclosures are available at . The Ontario Best Practices Research Initiative was funded by peer‐reviewed grants from the Canadian Institute for Health Research, the Ontario Ministry of Health and Long‐Term Care, the Canadian Arthritis Network, and unrestricted grants from Abbvie, Amgen, Aurora, Bristol‐Meyers Squibb, Celgene, Gilead, Hospira, Janssen, Lilly, Medexus, Merck, Novartis, Pfizer, Roche, Sandoz, Sanofi, and UCB. Xiuying Li, MD, MSc, Mohammad Movahedi, MD, PhD, Claire Bombardier, MD: Toronto General Hospital Research Institute, University Health Network, Toronto, Ontario, Canada ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 14 content type line 23 1Samar Aboulenain, MBBCh: St. Michael's Hospital, Toronto, Ontario, Canada; 2Xiuying Li, MD, MSc, Mohammad Movahedi, MD, PhD, Claire Bombardier, MD: Toronto General Hospital Research Institute, University Health Network, Toronto, Ontario, Canada; 3Bindee Kuriya, MD, SM: Sinai Health System, University of Toronto, Toronto, Ontario, Canada. Author disclosures are available at https://onlinelibrary.wiley.com/doi/10.1002/acr2.11629. |
ISSN: | 2578-5745 2578-5745 |
DOI: | 10.1002/acr2.11629 |