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

Continued inhibition of structural damage over 2 years in patients with rheumatoid arthritis treated with rituximab in combination with methotrexate.

机构信息

Metroplex Clinical Research Center, Dallas, Texas, USA.

出版信息

Ann Rheum Dis. 2010 Jun;69(6):1158-61. doi: 10.1136/ard.2009.119222. Epub 2010 May 3.

Abstract

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.

摘要

背景

利妥昔单抗可抑制类风湿关节炎(RA)患者的结构损伤,这些患者之前对肿瘤坏死因子(TNF)抑制剂反应不足。

目的

评估 2 年内的结构损伤进展情况。

方法

在接受基线后 1 张放射照片的意向治疗患者中(利妥昔单抗组 n=281;安慰剂组 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;患者有资格每 6 个月接受利妥昔单抗再治疗。到第 104 周时,82%的安慰剂人群接受了 >或= 1 剂利妥昔单抗。放射学终点包括第 104 周时总 Sharp 评分(TSS)、侵蚀和关节间隙狭窄评分的变化。

结果

第 104 周时,与安慰剂加 MTX相比,利妥昔单抗加 MTX组的 TSS(1.14 与 2.81;p<0.0001)、侵蚀评分(0.72 与 1.80;p<0.0001)和关节间隙狭窄评分(0.42 与 1.00;p<0.0009)的变化明显较低。在利妥昔单抗组中,1 年内关节损伤无进展的 87%患者在 2 年内仍未进展。

结论

利妥昔单抗加 MTX在对 TNF 抑制剂反应不足的 RA 患者中显示出对关节损伤进展的显著和持续的影响。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/065c/2935326/285d0acce40c/ard-69-06-1158-fig1.jpg

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