Tocilizumab as monotherapy or combination therapy for treating active rheumatoid arthritis: A meta-analysis of efficacy and safety reported in randomized controlled trials
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2016-09-22
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Abstract
Background: Previous studies in patients with rheumatoid arthritis (RA) have shown that switching to tocilizumab (TCZ) monotherapy (TCZMONO) or combination therapy (TCZCOMBI) with conventional synthetic disease-modifying anti-rheumatic drugs (csDMARDs) is efficacious in reducing disease activity in patients with inadequate response to csDMARDs. However, hitherto there is no consensus on whether TCZMONO is as effective as TCZCOMBI. The objective of this study was therefore to evaluate the efficacy and safety of TCZMONO versus add-on TCZCOMBI and both TCZ therapies versus continuing the current csDMARD therapy, by performing a systematic review and meta-analyses. Method: The MEDLINE, EMBASE and CENTRAL databases were searched until February 2016 for relevant randomized controlled trials (RCTs). We performed meta-analyses of Disease Activity Score in 28 joints (DAS28COMBI strategy. However, the risk of SAEs was also significantly higher using this strategy (RR 1.40; 95 % CI 1.03, 1.92, p=0.03). Pooled effect estimates showed statistical superiority of switching to either TCZ strategy compared to continuing csDMARD therapy. Conclusions: In the management of active RA, almost similar efficacy can be expected in patients unable to tolerate csDMARDs, who switch to TCZMONO compared to inadequate responders switching to add-on TCZCOMBI. Although TCZCOMBI is marginally superior to TCZMONO in achieving DAS28
Keywords
Biological, Disease-modifying anti-rheumatic drugs, Interleukin-6, Rheumatoid arthritis, Tocilizumab, Immunology and Allergy, Rheumatology, Immunology, Journal Article
Citation
Teitsma, X M, Marijnissen, A K A, Bijlsma, J W J, Lafeber, F P J & Jacobs, J W G 2016, 'Tocilizumab as monotherapy or combination therapy for treating active rheumatoid arthritis : A meta-analysis of efficacy and safety reported in randomized controlled trials', Arthritis Research & Therapy, vol. 18, 18:211. https://doi.org/10.1186/s13075-016-1108-9