Changes in Market Share of Biologic and Targeted Synthetic Disease Modifying Anti-Rheumatic Drugs for Treatment of Rheumatoid Arthritis: Results from the Ontario Best-Practice Research Initiative Database

2020 
OBJECTIVE For patients with Rheumatoid Arthritis (RA) who do not achieve adequate clinical response with combined conventional synthetic disease modifying anti-rheumatic drugs (csDMARDs), initiation of advanced therapies such as biologic DMARDs (bDMARDs) or targeted synthetic DMARDs (tsDMARDs) is recommended. Tumour necrosis factor inhibitors (TNFi) are the oldest, and most commonly used subgroup of advanced therapies. In the last decade, new non-TNFi advanced therapy options have become available. We described the relative use of TNFi vs. non-TNFi in Ontario-based practices from 2008-2017. METHODS Adult patients with RA enrolled in the Ontario Best Practices Research Initiative (OBRI) database who started bDMARDs or tsDMARDs anytime during, or within 30 days prior to enrollment were included. The proportion of patients treated with TNFi vs. non-TNFi agents between 2008 and 2017 was described for: all patients, and those initiating their first bDMARD/tsDMARD. All TNFi therapies are included. Non-TNFi included: Abatacept, Rituximab, Tocilizumab, and Tofacitinib. RESULTS A total of 1,057 patients were included of whom 72.0% were bDMARD/tsDMARD naive. In 2008, the relative non-TNFi use was 5.4% in all patients while it was 0% in bDMARD/tsDMARD-naive patients. By 2017, the proportion of patients using non-TNFi increased to 33.8% among all patients and 33.3% in bDMARD/tsDMARD-naive patients. CONCLUSION This descriptive analysis of data from the OBRI cohort reveals TNFi are still used in the majority of cases, however, there has been an increase in the use of non-TNFi therapies both overall and as first line advanced therapy. This trend towards non-TNFi therapies as first line advanced therapy may be partially explained by the shift in guideline recommendations from TNFi as first-line, to any of the advanced therapeutics.
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