TNFα antagonist continuation rates in 442 patients with inflammatory joint disease

被引:60
作者
Brocq, Olivier
Roux, Christian Hubert
Albert, Christine
Breuil, Veronique
Aknouche, Nicolas
Ruitord, Sandra
Mousnier, Aline
Euller-Ziegler, Liana
机构
[1] CHU Archet 1, Serv Rhumatol, F-06202 Nice 3, France
[2] Archet Teaching Hosp 1, Dept Pharm, F-06202 Nice 3, France
关键词
rheumatic disease; chronic inflammatory joint disease; TNF alpha antagonist; treatment continuation rate;
D O I
10.1016/j.jbspin.2006.06.011
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Objective: To evaluate TNF alpha. antagonist continuation rates in patients with rheumatoid arthritis (RA), ankylosing spondylitis (AS), or psoriatic arthritis (PsA). Methods: We retrospectively reviewed the charts of patients treated with etanercept, infliximab, or adalimumab at our teaching hospital. Drug continuation was evaluated using Kaplan-Meier survival curves. The logrank test was used to compare continuation rates. Results: We identified 442 patients who were prescribed 571 TNFa antagonist treatments between August 1999 and June 2005. Among them, 304 had RA, 92 AS, and 46 PsA. In the RA group, continuation rates were high with etanercept (n = 157; 87% after 12 months and 68% after 24 months) and adalimumab (n = 43, 83% and 66%) but significantly lower with infliximab (it = 104, 68% and 46%; P = 0.0001 vs. etanercept and P = 0.01 vs. adalimumab). In the AS group, in contrast, infliximab (n = 53) showed significantly higher continuation rates (89% and 83%) than did etanercept (n = 39; 76% after 12 months: P = 0.03). Overall continuation rates were higher in AS than in RA (P = 0.01). Conclusion: Continuation was better with etanercept than with infliximab in patients with RA, whereas the opposite was noted in patients with AS. (C) 2007 Elsevier Masson SAS. All rights reserved.
引用
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页码:148 / 154
页数:7
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