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利妥昔单抗联合甲氨蝶呤治疗早期活动性类风湿关节炎的疗效:IMAGE 试验。

Inhibition of joint damage and improved clinical outcomes with rituximab plus methotrexate in early active rheumatoid arthritis: the IMAGE trial.

机构信息

Division of Clinical Immunology and Rheumatology, Academic Medical Center/University of Amsterdam, Amsterdam, The Netherlands.

出版信息

Ann Rheum Dis. 2011 Jan;70(1):39-46. doi: 10.1136/ard.2010.137703. Epub 2010 Oct 11.

Abstract

OBJECTIVES

Rituximab is an effective treatment in patients with established rheumatoid arthritis (RA). The objective of the IMAGE study was to determine the efficacy of rituximab in the prevention of joint damage and its safety in combination with methotrexate (MTX) in patients initiating treatment with MTX.

METHODS

In this double-blind randomised controlled phase III study, 755 MTX-naïve patients with active RA were randomly assigned to MTX alone, rituximab 2×500 mg + MTX or rituximab 2×1000 mg + MTX. The primary end point at week 52 was the change in joint damage measured using a Genant-modified Sharp score.

RESULTS

249, 249 and 250 patients were randomly assigned to MTX alone, rituximab 2×500 mg + MTX or rituximab 2×1000 mg + MTX, respectively. At week 52, treatment with rituximab 2×1000 mg + MTX compared with MTX alone was associated with a reduction in progression of joint damage (mean change in total modified Sharp score 0.359 vs 1.079; p=0.0004) and an improvement in clinical outcomes (ACR50 65% vs 42%; p<0.0001); rituximab 2×500 mg + MTX improved clinical outcomes (ACR50 59% vs 42%; p<0.0001) compared with MTX alone but did not significantly reduce the progression of joint damage. Safety outcomes were similar between treatment groups.

CONCLUSIONS

Treatment with rituximab 2×1000 mg in combination with MTX is an effective therapy for the treatment of patients with MTX-naïve RA. ClinicalTrials.gov identifier NCT00299104.

摘要

目的

利妥昔单抗对已确诊的类风湿关节炎(RA)患者具有显著疗效。IMAGE 研究旨在评估利妥昔单抗联合甲氨蝶呤(MTX)治疗方案在预防关节损伤方面的疗效及其在 MTX 初治患者中的安全性。

方法

这是一项双盲、随机对照的 III 期临床研究,共纳入 755 例 MTX 初治、活动性 RA 患者,按 1:1:1 随机分配至 MTX 单药组、利妥昔单抗 2×500mg+MTX 组和利妥昔单抗 2×1000mg+MTX 组。主要终点为第 52 周时采用 Genant 改良 Sharp 评分法评估的关节损伤变化。

结果

755 例患者分别按 1:1:1 随机分配至 MTX 单药组、利妥昔单抗 2×500mg+MTX 组和利妥昔单抗 2×1000mg+MTX 组。第 52 周时,与 MTX 单药组相比,利妥昔单抗 2×1000mg+MTX 组患者的关节损伤进展程度显著降低(总改良 Sharp 评分变化均值 0.359 比 1.079,p=0.0004),临床疗效改善(ACR50 分别为 65%和 42%,p<0.0001);利妥昔单抗 2×500mg+MTX 组与 MTX 单药组相比,临床疗效也有所改善(ACR50 分别为 59%和 42%,p<0.0001),但对关节损伤进展的抑制作用不显著。各组间安全性结局相似。

结论

利妥昔单抗 2×1000mg 联合 MTX 治疗方案是 MTX 初治 RA 患者的有效治疗选择。临床试验注册号:NCT00299104。

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