Rituximab fixed retreatment versus on-demand retreatment in refractory rheumatoid arthritis: comparison of two B cell depleting treatment strategies
1 Department of Rheumatology, Leiden University Medical Center, The Netherlands
2 Department of Rheumatology & Clinical Immunology, University Medical Center Utrecht, The Netherlands
3 Musculoskeletal Research Group, Institute of Cellular Medicine, Newcastle University, UK
Correspondence to:
J M van Laar, Musculoskeletal Research Group, Institute of Cellular Medicine, Newcastle University, Newcastle upon Tyne, NE2 4HH, UK; j.m.van-laar@ncl.ac.uk
Accepted 4 September 2008
| The first 150 words of the full text of this article appear below. |
Rituximab, an anti-CD20 monoclonal antibody, has been approved for treatment in patients with rheumatoid arthritis (RA) who have failed treatment with tumour necrosis factor (TNF) blocking agents.1 Previous studies have demonstrated its safety, efficacy and prevention of radiographic progression;2 3 however few studies have yet addressed the timing of repeated courses of rituximab. A study in 22 patients with RA showed that treatment with repeated courses of rituximab over a 5-year follow-up period was safe and well tolerated4 and additionally an open-label extension study of 3 large randomised, double-blind studies in patients with RA showed that clinical efficacy was maintained with subsequent courses of rituximab, comparable to the first rituximab course, without increased additional safety concerns.5 Interestingly, one study reported that rituximab retreatment was more effective; however, this was in patients whose disease activity had not completely returned to baseline levels.6 Therefore, the preferred timing of repeated treatment courses of rituximab
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