首页> 外文期刊>The Journal of rheumatology >Improved health-related quality of life for patients with active rheumatoid arthritis receiving rituximab: Results of the Dose-Ranging Assessment: International Clinical Evaluation of Rituximab in Rheumatoid Arthritis (DANCER) Trial.
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Improved health-related quality of life for patients with active rheumatoid arthritis receiving rituximab: Results of the Dose-Ranging Assessment: International Clinical Evaluation of Rituximab in Rheumatoid Arthritis (DANCER) Trial.

机译:接受利妥昔单抗治疗的活动性类风湿关节炎患者的健康相关生活质量得到改善:剂量范围评估的结果:类风湿关节炎的利妥昔单抗国际临床评估(DANCER)试验。

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OBJECTIVE: To evaluate the effect of rituximab treatment on health-related quality of life (HRQOL) in patients with active rheumatoid arthritis (RA), who have had an inadequate response to disease-modifying antirheumatic drugs, including biologic agents. METHODS: A randomized, multicenter, double-blind, placebo-controlled clinical trial involving 367 rheumatoid factor-positive patients was conducted. Patients received 2 infusions 2 weeks apart of placebo (n 122), rituximab 500 mg (n without glucocorticoids. All patients received stable doses of methotrexate (10 25 mg/wk). Measures included SF-36, assessed at baseline and at 24 weeks, as well as the HAQ and FACIT-Fatigue scale assessed at baseline and monthly for 24 weeks. Patients exceeding prespecified minimal clinically important differences (MCID) were examined. Clinical efficacy measurements (ACR20/50/70 and EULAR responses) were compared with HRQOL outcomes. RESULTS: At 24 weeks, the rituximab 500 mg and 1000 mg groups both reported statistically significantly greater improvements on the SF-36 physical component summary (4.37 and 4.89 points higher, respectively, vs placebo; p < 0.001). SF-36 physical function, bodily pain, vitality, social function, and role-physical subscale scores also statistically significantly improved vs placebo. At 24 weeks, 62.6% and 67.2% of the rituximab 500 mg and 1000 mg groups, respectively, exceeded the MCID of 0.22 in HAQ (p < 0.001). For FACIT-Fatigue, 55.3% and 65.6% of patients exceeded the MCID of 3.5 points compared with 35.2% of placebo over 24 weeks (p < 0.001). ACR20/50/70 and EULAR responders demonstrated greater improvements in mean baseline to 24 week changes in SF-36 and FACIT-Fatigue scores compared with nonresponders (p < 0.05). CONCLUSION: Both rituximab doses in combination with methotrexate were effective in improving all HRQOL outcomes in patients with active RA consistent with clinical efficacy.
机译:目的:评估利妥昔单抗治疗对活动性类风湿关节炎(RA)患者的健康相关生活质量(HRQOL)的影响,所述类风湿关节炎患者对疾病缓解性抗风湿药(包括生物制剂)的反应不足。方法:进行了一项随机,多中心,双盲,安慰剂对照的临床试验,涉及367名类风湿因子阳性患者。患者每隔2周接受安慰剂(n 122),利妥昔单抗500 mg(n不使用糖皮质激素)的2次输注。所有患者均接受稳定剂量的甲氨蝶呤(10 25 mg / wk)。措施包括SF-36,在基线和第24周评估,以及在基线和每月24周评估的HAQ和FACIT疲劳量表,检查了超出预先确定的最小临床重要差异(MCID)的患者,并将临床疗效测量值(ACR20 / 50/70和EULAR反应)与HRQOL进行了比较结果:在第24周,利妥昔单抗500 mg和1000 mg组均报告了SF-36物理成分摘要的统计学改善显着(分别比安慰剂高4.37和4.89点; p <0.001)。与安慰剂相比,身体功能,身体疼痛,活力,社交功能和角色-身体下量表得分也有统计学上的显着改善,在第24周时,分别在500 mg和1000 mg利妥昔单抗组中分别有62.6%和67.2%在HAQ中修改了0.22的MCID(p <0.001)。对于FACIT-疲劳,在24周内,超过MCID 3.5分的患者分别占55.3%和65.6%,而安慰剂为35.2%(p <0.001)。与无应答者相比,ACR20 / 50/70和EULAR应答者显示SF-36和FACIT-疲劳评分的平均基线到24周变化的改善更大(p <0.05)。结论:两种利妥昔单抗联合甲氨蝶呤的剂量均可有效改善活动性RA患者的所有HRQOL结果,与临床疗效一致。

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