首页> 外文期刊>Annals of the Rheumatic Diseases: A Journal of Clinical Rheumatology and Connective Tissue Research >Continued inhibition of structural damage over 2 years in patients with rheumatoid arthritis treated with rituximab in combination with methotrexate.
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Continued inhibition of structural damage over 2 years in patients with rheumatoid arthritis treated with rituximab in combination with methotrexate.

机译:利妥昔单抗联合甲氨蝶呤治疗的类风湿关节炎患者在2年内持续抑制结构损伤。

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BACKGROUND: Rituximab inhibited structural damage at 1 year in patients with rheumatoid arthritis (RA) who had had a previous inadequate response to tumour necrosis factor (TNF) inhibitors. OBJECTIVE: To assess structural damage progression through 2 years. METHODS: Intention-to-treat patients with one post-baseline radiograph (rituximab n=281; placebo n=187) received background methotrexate (MTX) and were randomised to rituximab (2 x 1000 mg infusions, 2 weeks apart) or placebo; patients were eligible for rituximab re-treatment every 6 months. By week 104, 82% of the placebo population had received > or = 1 dose of rituximab. Radiographic end points included the change in total Sharp score (TSS), erosion and joint space narrowing scores at week 104. RESULTS: At week 104, significantly lower changes in TSS (1.14 vs 2.81; p<0.0001), erosion score (0.72 vs 1.80; p<0.0001) and joint space narrowing scores (0.42 vs 1.00; p<0.0009) were observed with rituximab plus MTX vs placebo plus MTX. Within the rituximab group, 87% who had no progression of joint damage at 1 year remained non-progressive at 2 years. CONCLUSIONS: Rituximab plus MTX demonstrated significant and sustained effects on joint damage progression in patients with RA and a previously inadequate response to TNF inhibitors.
机译:背景:利妥昔单抗可抑制类风湿关节炎(RA)患者在1年以前对肿瘤坏死因子(TNF)抑制剂反应不足的结构损伤。目的:评估2年内结构性损伤的进展。方法:对有意向治疗的患者进行基线后X线片检查(利妥昔单抗n = 281;安慰剂n = 187)接受背景甲氨蝶呤(MTX)治疗,并随机分配至利妥昔单抗(2 x 1000 mg输注,间隔2周)或安慰剂。患者每6个月有资格接受利妥昔单抗再治疗。到第104周时,有82%的安慰剂人群接受了≥1剂量的利妥昔单抗。影像学终点包括第104周时的总体Sharp评分(TSS),糜烂和关节间隙狭窄评分的变化。结果:第104周时,TSS的变化(1.14 vs 2.81; p <0.0001),糜烂评分(0.72 vs利妥昔单抗加MTX对比安慰剂加MTX观察到1.80; p <0.0001)和关节间隙变窄评分(0.42 vs 1.00; p <0.0009)。在利妥昔单抗组中,在1年时无关节损伤进展的87%在2年时仍未进展。结论:利妥昔单抗联合MTX对RA患者先前对TNF抑制剂的反应不足,对关节损伤进展具有显着而持续的影响。

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