Two-Year Clinical and Radiographic Results With Combination Etanercept-Methotrexate Therapy Versus Monotherapy in Early Rheumatoid Arthritis

被引:99
作者
Emery, Paul [1 ]
Breedveld, Ferdinand [2 ]
van der Heijde, Desiree [2 ]
Ferraccioli, Gianfranco [3 ]
Dougados, Maxime [4 ,5 ]
Robertson, Deborah [6 ]
Pedersen, Ronald [6 ]
Koenig, Andrew S. [6 ]
Freundlich, Bruce [6 ]
机构
[1] Univ Leeds, Leeds, W Yorkshire, England
[2] Leiden Univ Med Ctr, Leiden, Netherlands
[3] Univ Cattolica Sacro Cuore, CIC, I-00168 Rome, Italy
[4] Hop Cochin, Assistance Publ Hop Paris, F-75674 Paris, France
[5] Univ Paris 05, Paris, France
[6] Pfizer Inc, Collegeville, PA USA
来源
ARTHRITIS AND RHEUMATISM | 2010年 / 62卷 / 03期
关键词
MODIFYING ANTIRHEUMATIC DRUGS; RANDOMIZED CONTROLLED-TRIAL; DOUBLE-BLIND; READ RADIOGRAPHS; HEIJDE METHOD; FOLLOW-UP; DISEASE; PROGRESSION; REMISSION; ADALIMUMAB;
D O I
10.1002/art.27268
中图分类号
R5 [内科学];
学科分类号
100201 [内科学];
摘要
Objective. To evaluate how continuation of and alterations to initial year 1 combination etanercept-methotrexate (MTX) therapy and MTX monotherapy regimens affect long-term remission and radiographic progression in early, active rheumatoid arthritis. Methods. Subjects were randomized at baseline for the entire 2-year period; those who completed 1 year of treatment with combination or MTX monotherapy entered year 2. The original combination group either continued combination therapy (the EM/EM group; n = 111) or received etanercept monotherapy (the EM/E group; n = 111) in year 2; the original MTX monotherapy group either received combination therapy (the M/EM group; n = 90) or continued monotherapy (the M/M group; n = 99) in year 2. Efficacy end points included remission (a Disease Activity Score in 28 joints [DAS28] < 2.6) and radiographic nonprogression (change in the modified Sharp/van der Heijde score <= 0.5) at year 2. A last observation carried forward analysis from the modified intention-to-treat population (n = 398) and a post hoc nonresponder imputation (NRI) analysis (n = 528) were performed for remission. Results. At year 2, DAS28 remission was achieved by 62/108, 54/108, 51/88, and 33/94 subjects in the EM/EM, EM/E, M/EM, and M/M groups, respectively (P < 0.01 for the EM/EM and M/EM groups versus the M/M group). This effect was corroborated by a more conservative post hoc 2-year NRI analysis, with remission observed in 59/131, 50/134, 48/133, and 29/130 of the same respective groups (P < 0.05 for each of the EM/EM, EM/E, and M/EM groups versus the M/M group). The proportions of subjects achieving radiographic nonprogression (n = 360) were 89/99, 74/99, 59/79, and 56/83 in the EM/EM (P < 0.01 versus each of the other groups), EM/E, M/EM, and M/M groups, respectively. No new safety signals or between-group differences in serious adverse events were seen. Conclusion. Early sustained combination etanercept-MTX therapy was consistently superior to MTX monotherapy. Combination therapy resulted in important clinical and radiographic benefits over 2 study years, without significant additional safety risk.
引用
收藏
页码:674 / 682
页数:9
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