Comparison of tocilizumab monotherapy versus methotrexate monotherapy in patients with moderate to severe rheumatoid arthritis: the AMBITION study

被引:591
作者
Jones, G. [1 ]
Sebba, A. [2 ]
Gu, J. [3 ]
Lowenstein, M. B. [4 ]
Calvo, A. [5 ]
Gomez-Reino, J. J. [6 ]
Siri, D. A. [7 ]
Tomsic, M. [8 ]
Alecock, E. [9 ]
Woodworth, T. [9 ]
Genovese, M. C. [10 ]
机构
[1] Univ Tasmania, Menzies Res Inst, Hobart, Tas 7001, Australia
[2] Arthrit Res Florida, Palm Harbor, FL USA
[3] Sun Yat Sen Univ, Affiliated Hosp 3, Dept Rheumatol, Guangzhou 510275, Guangdong, Peoples R China
[4] Arthrit Ctr, Palm Harbor, FL USA
[5] San Felipe Clin, Lima, Peru
[6] Univ Santiago de Compostela, Santiago De Compostela, Spain
[7] CAICI Inst, Rosario, Argentina
[8] Univ Med Ctr, Dept Rheumatol, Ljubljana, Slovenia
[9] Roche Prod Ltd, Welwyn Garden City, England
[10] Stanford Univ, Med Ctr, Div Rheumatol & Immunol, Palo Alto, CA 94304 USA
关键词
RECEIVING CONCOMITANT METHOTREXATE; INTERLEUKIN-6 RECEPTOR INHIBITION; DOUBLE-BLIND; DISEASE-ACTIVITY; RADIOLOGICAL PROGRESSION; MONOCLONAL-ANTIBODY; CLINICAL-TRIAL; LIPID PROFILE; PLACEBO; MULTICENTER;
D O I
10.1136/ard.2008.105197
中图分类号
R5 [内科学];
学科分类号
100201 [内科学];
摘要
Background: The anti-interleukin (IL) 6 receptor antibody tocilizumab inhibits signalling of IL6, a key cytokine in rheumatoid arthritis (RA) pathogenesis. Objective: To evaluate through the AMBITION study the efficacy and safety of tocilizumab monotherapy versus methotrexate in patients with active RA for whom previous treatment with methotrexate/biological agents had not failed. Methods: This 24-week, double-blind, double-dummy, parallel-group study, randomised 673 patients to either tocilizumab 8 mg/kg every 4 weeks, or methotrexate, starting at 7.5 mg/week and titrated to 20 mg/week within 8 weeks, or placebo for 8 weeks followed by tocilizumab 8 mg/kg. The primary end point was the proportion of patients achieving American College of Rheumatology (ACR) 20 response at week 24. Results: The intention-to-treat analysis demonstrated that tocilizumab was better than methotrexate treatment with a higher ACR20 response (69.9 vs 52.5%; p<0.001), and 28-joint Disease Activity Score (DAS28) <2.6 rate (33.6 vs 12.1%) at week 24. Mean high-sensitivity C-reactive protein was within the normal range from week 12 with tocilizumab, whereas levels remained elevated with methotrexate. The incidence of serious adverse events with tocilizumab was 3.8% versus 2.8% with methotrexate (p=0.50), and of serious infections, 1.4% versus 0.7%, respectively. There was a higher incidence of reversible grade 3 neutropenia (3.1% vs 0.4%) and increased total cholesterol >= 240 mg/dl (13.2% vs 0.4%), and a lower incidence of alanine aminotransferase elevations >3x-<5x upper limit of normal (1.0% vs 2.5%), respectively. Conclusion: Tocilizumab monotherapy is better than methotrexate monotherapy, with rapid improvement in RA signs and symptoms, and a favourable benefit-risk, in patients for whom treatment with methotrexate or biological agents has not previously failed.
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页码:88 / 96
页数:9
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