Clinical Research, Merck Sharp & Dohme Corp, Whitehouse Station, NJ, USA.
J Allergy Clin Immunol. 2012 Nov;130(5):1071-1077.e10. doi: 10.1016/j.jaci.2012.07.057. Epub 2012 Oct 1.
Classifying asthma severity or activity has evolved, but there are no published weighted composite measures of asthma disease activity that account for the relative importance of the many individual clinical variables that are widely used.
We sought to develop a weighted and responsive measure of asthma disease activity.
Discriminant and multiple regression analyses based on 2 previously conducted clinical trials were used to develop the Asthma Disease Activity Score (ADAS-6).
The ADAS-6 demonstrated content validity because its components assess different manifestations of asthma: FEV(1) (percent predicted), Asthma Quality of Life Questionnaire-Symptom domain, rescue β-agonist use, nocturnal awakenings, peak expiratory flow diurnal variability, and rescue β-agonist use diurnal variability. The ADAS-6 demonstrated cross-sectional and longitudinal validity. It was discriminating: it distinguished levels of disease activity and response to different treatment intensities (P < .0001). Similar results were obtained with an independent clinical trial. The ADAS-6 was highly responsive to treatment effects, with a standardized effect size exceeding that of other widely used outcome measures. Using ADAS-6 as the primary end point in the montelukast pivotal trials would have significantly reduced the sample size needed to detect a comparable change in outcome. Furthermore, increments in the ADAS-6 predicted the risk of future asthma attacks. A simplified Asthma Disease Activity Score 4-variable version (ADAS-4) demonstrated similar measurement properties.
The ADAS-6 and ADAS-4 are novel, weighted, and responsive measures of asthma disease activity. Use of these measures in clinical trials might better separate treatment effects, predict future asthma attacks, and substantially reduce sample size.
哮喘严重程度或活动度的分类已经演变,但目前尚无综合衡量哮喘疾病活动度的加权复合指标,这些指标需要考虑到广泛应用的许多个体临床变量的相对重要性。
我们旨在开发一种加权且敏感的哮喘疾病活动度衡量指标。
采用基于两项先前进行的临床试验的判别分析和多元回归分析来开发哮喘疾病活动评分(ADAS-6)。
ADAS-6 具有内容效度,因为其组成部分评估了哮喘的不同表现:FEV1(预测百分比)、哮喘生活质量问卷-症状域、急救β激动剂使用、夜间觉醒、呼气峰流速日间变异率和急救β激动剂使用日间变异率。ADAS-6 具有横断面和纵向有效性。它具有区分能力:能够区分不同的疾病活动水平和对不同治疗强度的反应(P<0.0001)。在一项独立的临床试验中也得到了类似的结果。ADAS-6 对治疗效果高度敏感,其标准化效应量大于其他广泛使用的结局衡量指标。在孟鲁司特关键性试验中,将 ADAS-6 作为主要终点,可显著减少检测可比结局变化所需的样本量。此外,ADAS-6 的增加预测了未来哮喘发作的风险。简化的哮喘疾病活动评分 4 变量版本(ADAS-4)显示出相似的测量特性。
ADAS-6 和 ADAS-4 是新颖的、加权的、敏感的哮喘疾病活动度衡量指标。在临床试验中使用这些指标可能会更好地分离治疗效果、预测未来的哮喘发作,并显著减少样本量。