Humbert M, Berger W, Rapatz G, Turk F
Université Paris-Sud 11, Service de Pneumologie, Hôpital Antoine Béclère, Clamart, France.
Allergy. 2008 May;63(5):592-6. doi: 10.1111/j.1398-9995.2008.01654.x. Epub 2008 Mar 18.
Omalizumab is efficacious in the treatment of moderate-to-severe and severe persistent allergic (immunoglobulin E-mediated) asthma, reducing exacerbations, emergency visits and improving quality of life (QoL). However, as exacerbations are relatively infrequent, assessment of efficacy on day-to-day symptoms is warranted.
To investigate the effect of add-on omalizumab on day-to-day symptoms, and how they correlate with QoL in severe persistent asthma.
The correlation between asthma symptom scores and QoL [Asthma Quality of Life Questionnaire (AQLQ)] was assessed. Symptom-free days (total symptom score = 0) and symptom-controlled days (definition 1: total symptom score </=1; and definition 2: morning peak expiratory flow >/=90% of baseline, daytime asthma score </=1 and night-time asthma score = 0) were compared between the omalizumab-treated group, omalizumab responders and placebo.
Four hundred and nineteen patients (omalizumab, n = 209; placebo, n = 210) were included in the efficacy analyses, and 61% (118/195) of patients with response data were classified as responders. Total symptom score strongly correlated with AQLQ overall and symptom scores and individual domains. AQLQ overall score correlated well with symptom scores. Responders had significantly more symptom-free days than the omalizumab-treated and placebo groups (45.8%, 37.2% and 22.6% respectively), and more symptom-controlled days (definition 1: 56.1%, 47.9% and 35.3%, respectively, and definition 2: 50.8%, 43.9% and 28.0%, respectively).
In patients with inadequately controlled severe persistent asthma, day-to-day symptoms correlate well with QoL. Add-on omalizumab significantly improves day-to-day symptoms compared with placebo. Further improvement in responders confirms the physician's assessment as a response measure.
奥马珠单抗在治疗中度至重度及重度持续性过敏性(免疫球蛋白E介导)哮喘方面有效,可减少病情加重、急诊就诊次数并改善生活质量(QoL)。然而,由于病情加重相对不常见,因此有必要评估其对日常症状的疗效。
研究加用奥马珠单抗对重度持续性哮喘日常症状的影响,以及这些症状与生活质量的相关性。
评估哮喘症状评分与生活质量[哮喘生活质量问卷(AQLQ)]之间的相关性。比较奥马珠单抗治疗组、奥马珠单抗反应者和安慰剂组的无症状天数(总症状评分为0)和症状控制天数(定义1:总症状评分≤1;定义2:早晨呼气峰值流量≥基线的90%,白天哮喘评分为≤1且夜间哮喘评分为0)。
419例患者(奥马珠单抗组,n = 209;安慰剂组,n = 210)纳入疗效分析,61%(118/195)有反应数据的患者被分类为反应者。总症状评分与AQLQ总体、症状评分及各个领域均密切相关。AQLQ总体评分与症状评分相关性良好。反应者的无症状天数显著多于奥马珠单抗治疗组和安慰剂组(分别为45.8%、37.2%和22.6%),症状控制天数也更多(定义1:分别为56.1%、47.9%和35.3%;定义2:分别为50.8%、43.9%和28.0%)。
在重度持续性哮喘控制不佳的患者中,日常症状与生活质量密切相关。与安慰剂相比,加用奥马珠单抗可显著改善日常症状。反应者的进一步改善证实了医生的评估可作为一种反应指标。