Division of Clinical Immunology and Rheumatology, Academic Medical Centre/University of Amsterdam, Amsterdam, The Netherlands.
Ann Rheum Dis. 2012 Mar;71(3):351-7. doi: 10.1136/annrheumdis-2011-200170. Epub 2011 Oct 19.
In the IMAGEstudy, rituximab plus methotrexate (MTX) inhibited joint damage and improved clinical outcomes at 1 year in MTX-naïve patients with early active rheumatoid arthritis.
The aim of this study was to assess joint damage progression and clinical outcomes over 2 years.
Patients (n=755) were randomised to receive rituximab 2×500 mg+MTX, 2×1000 mg+MTX or placebo+MTX. The placebo-controlled period continued to week 104. Two-year end points were defined as secondary or exploratory and included change in total Genant-modified Sharp score (mTSS), total erosion score and joint space narrowing score from baseline to week 104. Clinical efficacy and physical function end points were also assessed.
At 2 years, rituximab 2×1000 mg+MTX maintained inhibition of progressive joint damage versus MTX alone (mTSS change 0.41 vs 1.95; p<0.0001 (79% inhibition)), and a higher proportion of patients receiving rituximab 2×1000 mg+MTX had no radiographic progression over 2 years compared with those receiving MTX alone (57% vs 37%; p<0.0001). Contrary to 1-year results, exploratory analysis of rituximab 2×500 mg+MTX at 2 years showed that progressive joint damage was slowed by ∼61% versus placebo+MTX (mTSS, exploratory p=0.0041). Improvements in clinical signs and symptoms and physical function seen after 1 year in rituximab-treated patients versus those receiving placebo were maintained at year 2. Safety profiles were similar between groups.
Treatment with rituximab 2×1000 mg+MTX was associated with sustained improvements in radiographic, clinical and functional outcomes over 2 years. Clinical trials.gov identifier NCT00299104.
在 IMAGE 研究中,利妥昔单抗联合甲氨蝶呤(MTX)可抑制新诊断的早期活动性类风湿关节炎患者的关节损伤,并改善 1 年的临床结局。
本研究旨在评估 2 年时的关节损伤进展和临床结局。
将 755 例患者随机分为利妥昔单抗 2×500mg+MTX、2×1000mg+MTX 或安慰剂+MTX 组。安慰剂对照期持续至第 104 周。将 2 年的终点定义为次要或探索性终点,包括从基线到第 104 周时总 Genant 改良 Sharp 评分(mTSS)、总侵蚀评分和关节间隙狭窄评分的变化。同时评估临床疗效和躯体功能终点。
2 年时,与 MTX 单药组相比,利妥昔单抗 2×1000mg+MTX 持续抑制关节损伤进展(mTSS 变化 0.41 对 1.95;p<0.0001(抑制率 79%)),并且接受利妥昔单抗 2×1000mg+MTX 治疗的患者在 2 年内有更多的患者无影像学进展(57%对 37%;p<0.0001)。与 1 年的结果相反,对利妥昔单抗 2×500mg+MTX 治疗的探索性分析显示,与安慰剂+MTX 组相比,2 年时关节损伤进展速度减慢约 61%(mTSS,探索性 p=0.0041)。1 年时接受利妥昔单抗治疗的患者与接受安慰剂的患者相比,临床症状和体征以及躯体功能的改善在第 2 年时得到了维持。各组的安全性特征相似。
利妥昔单抗 2×1000mg+MTX 治疗可使影像学、临床和功能结局在 2 年内持续改善。临床试验注册编号 NCT00299104。