Indirect Comparison of Tocilizumab and Other Biologic Agents in Patients with Rheumatoid Arthritis and Inadequate Response to Disease-Modifying Antirheumatic Drugs

被引:80
作者
Bergman, Gert J. D. [7 ]
Hochberg, Marc C. [2 ,3 ]
Boers, Maarten [4 ]
Wintfeld, Neil [5 ]
Kielhorn, Adrian [6 ]
Jansen, Jeroen P. [1 ]
机构
[1] Mapi Values, Boston, MA 02114 USA
[2] Univ Maryland, Sch Med, Dept Med, Baltimore, MD 21201 USA
[3] Univ Maryland, Sch Med, Dept Epidemiol & Prevent Med, Baltimore, MD 21201 USA
[4] Vrije Univ Amsterdam, Med Ctr, Dept Epidemiol & Biostat, Amsterdam, Netherlands
[5] Roche, Nutley, NJ USA
[6] Roche, Basel, Switzerland
[7] Mapi Values, Houten, Netherlands
关键词
rheumatoid arthritis; tocilizumab; biologic DMARDs; mixed-treatment comparison; ANTITUMOR NECROSIS FACTOR; RECEIVING CONCOMITANT METHOTREXATE; INTERLEUKIN-6 RECEPTOR INHIBITION; ALPHA MONOCLONAL-ANTIBODY; DOUBLE-BLIND; FUSION PROTEIN; PHASE-III; EFFICACY; PLACEBO; ETANERCEPT;
D O I
10.1016/j.semarthrit.2009.12.002
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Objectives: To compare the patterns of American College of Rheumatology (ACR) response between tocilizumab and other biologic agents in patients with rheumatoid arthritis who have inadequate response to disease-modifying antirheumatic drugs (DMARD-IR). Methods: Systematic literature review identified similarly designed double-blind, randomized, placebo-controlled trials over an 18-year period that investigated the effectiveness of abatacept (2), rituximab (2), and TNF-alpha inhibitors etanercept, infliximab, and adalimumab (11) in DMARD-IR patients; data from 3 placebo-controlled, phase 3 trials for tocilizumab, a newly developed IL-6 inhibitor, were included. The endpoint of interest was ACR20/50/70 response criteria at 24 to 30 weeks. Results were analyzed simultaneously using Bayesian mixed-treatment comparison techniques. Nonoverlapping ACR response rates (<ACR20, ACR20-50, ACR50-70, >ACR70) for each agent were compared among treatments to identify differences in ACR response pattern. Separate analyses of overlapping ACR20/50/70 responses were conducted to identify the source of any differences. Results were expressed as relative risk of ACR20/50/70 response and associated 95% credible interval (Cr1). Results: Patterns across nonoverlapping ACR response levels varied significantly across treatments. In subsequent analyses, the effectiveness of tocilizumab appeared to be comparable to that of other biologic agents for ACR20 and ACR50 responses but greater for ACR70. Specifically, tocilizumab had greater ACR70 responses than both TNF-alpha inhibitors (relative risk = 1.8; CrI = 1.2, 2.6) and abatacept (relative risk = 2.0; CrI = 1.3, 3.1). Conclusions: Among DMARD-IR patients, tocilizumab shows a pattern of response that differs from that of other biologic agents. Post-hoc analyses suggest that the difference lies in a higher likelihood of ACR70 response with tocilizumab. (C) 2010 Elsevier Inc. All rights reserved. Semin Arthritis Rheum 39:425-441
引用
收藏
页码:425 / 441
页数:17
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