Yount S, Sorensen M V, Cella D, Sengupta N, Grober J, Chartash E K
The Center on Outcomes, Research and Education, Evanston Northwestern Healthcare, Evanston, IL 60201, USA.
Clin Exp Rheumatol. 2007 Nov-Dec;25(6):838-46.
Fatigue is an important systemic symptom of rheumatoid arthritis (RA) but has rarely been evaluated consistently after initiation of treatment in RA patients. This study examined the effects of adalimumab (HUMIRA, Abbott Laboratories, Abbott Park, IL, USA), a fully human, anti-tumor necrosis factor (anti-TNF) monoclonal antibody, on reducing fatigue in patients with RA.
A total of 1526 patients with RA were enrolled in 3 randomized, placebo-controlled clinical trials of adalimumab versus placebo plus methotrexate (MTX) or placebo plus standard antirheumatic therapies. Fatigue was assessed with the Functional Assessment of Chronic Illness Therapy (FACIT) fatigue scale questionnaire (which has been validated in RA) at baseline, mid-study, and at the end of the study. Logistic regression models were constructed using baseline demographic variables to test for treatment effect. In addition, sensitivity analyses were performed to determine the robustness of the data.
At baseline in the 3 trials, patients' fatigue ranged from 27.9-29.7, representing considerable fatigue on the FACIT fatigue scale. Fatigue was significantly and consistently reduced in adalimumab-treated patients in the 3 clinical trials. Relative to placebo plus MTX, the adalimumab 40-mg-every-other-week dosage group reported statistically significantly less fatigue at all time points post-baseline. Improvements between adalimumab and placebo ranged from 3-7 points across all 3 trials, with a 3-4-point change representing a minimum clinically important difference.
Adalimumab treatment was shown to significantly reduce fatigue in patients with moderate to severe RA. Changes in fatigue in all 3 trials were found to be clinically important.
疲劳是类风湿关节炎(RA)的一种重要全身症状,但在RA患者开始治疗后很少得到持续评估。本研究考察了全人源抗肿瘤坏死因子(anti-TNF)单克隆抗体阿达木单抗(修美乐,美国雅培公司,伊利诺伊州雅培公园)对减轻RA患者疲劳的作用。
共有1526例RA患者参加了3项阿达木单抗与安慰剂加甲氨蝶呤(MTX)或安慰剂加标准抗风湿疗法对比的随机、安慰剂对照临床试验。在基线、研究中期和研究结束时,采用慢性病治疗功能评估(FACIT)疲劳量表问卷(已在RA中得到验证)对疲劳进行评估。使用基线人口统计学变量构建逻辑回归模型以检验治疗效果。此外,还进行了敏感性分析以确定数据的稳健性。
在3项试验的基线期,患者的疲劳程度在27.9 - 29.7之间,在FACIT疲劳量表上显示有相当程度的疲劳。在3项临床试验中,接受阿达木单抗治疗的患者疲劳程度显著且持续降低。相对于安慰剂加MTX,阿达木单抗每两周40 mg剂量组在基线后所有时间点报告的疲劳程度在统计学上均显著更低。在所有3项试验中,阿达木单抗与安慰剂之间的改善幅度为3 - 7分,3 - 4分的变化代表最小临床重要差异。
结果显示,阿达木单抗治疗可显著减轻中重度RA患者的疲劳。所有3项试验中疲劳程度的变化均具有临床重要性。