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首页> 外文期刊>Dermatology and Therapy >Dupilumab Improves General Health-Related Quality-of-Life in Patients with Moderate-to-Severe Atopic Dermatitis: Pooled Results from Two Randomized, Controlled Phase 3 Clinical Trials
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Dupilumab Improves General Health-Related Quality-of-Life in Patients with Moderate-to-Severe Atopic Dermatitis: Pooled Results from Two Randomized, Controlled Phase 3 Clinical Trials

机译:Dupilumab可改善中度至重度特应性皮炎患者的一般健康相关生活质量:两项随机对照三期临床试验的汇总结果

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IntroductionPatients with moderate-to-severe atopic dermatitis (AD) report a multidimensional disease burden that includes impaired health-related quality-of-life (HRQoL). Changes in overall health status and specific dimensions that contribute to HRQoL were evaluated in adults with moderate-to-severe AD who participated in phase 3 clinical trials of dupilumab, which is a fully human monoclonal antibody that inhibits signaling of cytokines IL-4 and IL-13. MethodsTwo dupilumab phase 3 clinical trials of identical design included the 5-dimension 3-level EuroQol (EQ-5D) as a measure of HRQoL. EQ-5D data from the two trials were pooled in an analysis that, using analysis of covariance, compared subcutaneous dupilumab 300?mg once weekly (qw) or every 2?weeks (q2w) versus placebo for EQ-5D utility score change from baseline overall and for clinical responders. The proportions of patients who reported different levels of problems on the individual dimension of the EQ-5D were also compared by treatment group. ResultsPatients ( n =?1379) were 57.9% male with a mean (SD) age of 38.3 (14.3) years; baseline EQ-5D utility scores ranged from 0.611 to 0.629 across treatment groups. EQ-5D least squares mean change from baseline at week 16 was 0.031 with placebo, and was significantly greater with dupilumab qw (0.207) and q2w (0.210) (both P ConclusionIn adults with moderate-to-severe AD, dupilumab resulted in improvements in HRQoL that were statistically significant relative to placebo and were clinically meaningful. FundingSanofi and Regeneron Pharmaceuticals, Inc. Trial registrationClinicalTrials.gov identifiers, NCT02277743 and NCT02277769, EudraCT Numbers 2014-001198-15 and 2014-002619-40.
机译:简介患有中度至重度的特应性皮炎(AD)的患者报告了多维疾病负担,其中包括与健康相关的生活质量(HRQoL)受损。在参加dupilumab 3期临床试验的成年至中度AD成年人中评估了导致HRQoL的总体健康状况和特定尺寸的变化,dupilumab是一种抑制细胞因子IL-4和IL信号传导的完全人单克隆抗体。 -13。方法两项设计相同的dupilumab 3期临床试验包括5维3级EuroQol(EQ-5D)作为HRQoL的量度。来自两项试验的EQ-5D数据进行了汇总分析,使用协方差分析比较了每周一次(qw)或每2周一次(q2w)皮下注射dupilumab 300?mg与安慰剂相比,EQ-5D效用得分从基线变化整体和针对临床反应者。还按治疗组比较了在EQ-5D个体维度上报告了不同水平问题的患者比例。结果患者(n = 1379)为男性的57.9%,平均(SD)年龄为38.3(14.3)岁;各治疗组的EQ-5D基线效用得分在0.611至0.629之间。 EQ-5D最小二乘均值在第16周时与安慰剂相比从基线的平均变化为0.031,而dupilumab qw(0.207)和q2w(0.210)则显着更大(均为P结论)在中至重度AD的成年人中,dupilumab改善了相对于安慰剂而言,HRQoL具有统计学意义,并且在临床上具有重要意义FundingSanofi和Regeneron Pharmaceuticals,Inc.试用registrationClinicalTrials.gov标识符,NCT02277743和NCT02277769,EudraCT编号2014-001198-15和2014-002619-40。

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