Guest guest Posted January 5, 2010 Report Share Posted January 5, 2010 Have We ARRIVEd at Initiating Abatacept Right After Anti-TNF Treatment Failure? The 6-Month Safety and Efficacy of Abatacept in Patients With Rheumatoid Arthritis Who Underwent a Washout After Anti-tumour Necrosis Factor Therapy or Were Directly Switched to Abatacept: the ARRIVE Trial Deane, MD Posted: 28 Dec 2009 Schiff M, Pritchard C, Huffstutter JE, et al Ann Rheum Dis. 2009; 68:1708-1714 Study Summary Patients with rheumatoid arthritis (RA) fail anti-tumor necrosis factor (TNF) therapy for a variety of reasons, including lack of efficacy, drug intolerance, and adverse events (AEs). Additional biologic therapies, such as the selective T-cell costimulation modulator abatacept, are approved for use after failure of an anti-TNF agent. However, little data are available for when abatacept may be safely started after failure of an anti-TNF agent. To address this issue, the safety and efficacy of abatacept given either right after cessation or after a washout period were evaluated in patients with RA post anti-TNF therapy. Some disagreement exists between the introduction and the methods; overall, it appears that patients qualified for the study if they had inadequate response of at least 3 months of an anti-TNF agent or had safety or tolerability issues. Patients had a disease activity score in 28 joints (DAS28 [C-reactive protein]) of ≥ 5.1, which is indicative of active disease. Background non-biological disease-modifying antirheumatic drugs had to be stable for about 1 month before enrollment. A fixed dose of abatacept of approximately 10 mg/kg was administered in an open-label fashion. ****************************************** Read the full article here: http://www.medscape.com/viewarticle/714092 Not an MD Quote Link to comment Share on other sites More sharing options...
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