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首页> 外文期刊>Allergy and asthma proceedings >Efficacy of omalizumab in cat-allergic patients with moderate-to-severe persistent asthma.
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Efficacy of omalizumab in cat-allergic patients with moderate-to-severe persistent asthma.

机译:奥马珠单抗在猫过敏性中重度持续哮喘患者中的疗效。

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Cat allergen (Fel d 1) is a pervasive and common trigger of exacerbations in sensitized patients with IgE-mediated asthma. This study was designed to evaluate the effect on asthma-related outcome measures of adding omalizumab to current treatment in patients with moderate-to-severe persistent asthma and cat allergen sensitivity. A pooled analysis was conducted of two double-blind, placebo-controlled, 28-week pivotal U.S. registration trials. In all patients, asthma was inadequately controlled with moderate-high dose inhaled corticosteroids. Patients were randomized to receive subcutaneous omalizumab (minimum, 0.016 mg/kg per IgE IU/mL every 4 weeks) or matched placebo. The effects of omalizumab on asthma-related outcomes were assessed for patients with cat allergen sensitivity (n = 811), identified by positive skin-prick test. The mean number of asthma exacerbations requiring treatment with systemic steroid bursts in cat allergen-sensitive patients was lower in those receiving omalizumab versus placebo (0.6 versus 1.3, respectively; relative risk = 0.50, p < 0.001). Compared with placebo, omalizumab treatment led to significantly lower asthma symptom scores (least squares means (LSMs) treatment difference [95% confidence interval {CI}]: -0.57 [-0.77, -0.37]; p < 0.001), less rescue medication use (LSMs treatment difference [95% CI]: -0.75 puffs of rescue beta-agonist per day [-1.04, -0.46]; p < 0.001), and improvement in forced expiratory volume in 1 second (LSMs treatment difference [95% CI]: 100.84 mL [51.86, 149.81]; p < 0.001). Patient and investigator global evaluations of treatment effectiveness paralleled these outcomes. Omalizumab improved asthma control by reducing exacerbations and decreasing symptoms in cat-allergic patients with moderate-to-severe persistent IgE-mediated asthma.
机译:猫过敏原(Fel d 1)是致敏的IgE介导哮喘患者普遍加重病情的诱因。本研究旨在评估在中至重度持续性哮喘和猫过敏原敏感性患者中加入奥马珠单抗治疗当前与哮喘有关的结局指标的效果。对两项双盲,安慰剂对照,为期28周的关键美国注册试验进行了汇总分析。在所有患者中,中高剂量吸入糖皮质激素均不能充分控制哮喘。患者被随机分配皮下注射奥马珠单抗(最低剂量,每4周每IgE IU / mL 0.016 mg / kg)或匹配的安慰剂。对猫过敏原敏感性(n = 811)的患者进行了奥马珠单抗对哮喘相关结局的影响评估,通过皮肤点刺试验确定。接受奥马珠单抗治疗的猫过敏患者中,需要全身性类固醇爆发治疗的哮喘急性发作的平均人数低于安慰剂组(分别为0.6和1.3;相对风险= 0.50,p <0.001)。与安慰剂相比,奥马珠单抗治疗可显着降低哮喘症状评分(最小二乘均数(LSMs)治疗差异[95%置信区间{CI}]:-0.57 [-0.77,-0.37]; p <0.001),急救药物较少使用(LSMs治疗差异[95%CI]:每天-0.75扑救性β-激动剂[-1.04,-0.46]; p <0.001),并在1秒内改善强制呼气量(LSMs治疗差异[95% CI:100.84mL [51.86,149.81]; p <0.001)。患者和研究者对治疗效果的整体评估与这些结果平行。奥马珠单抗通过减轻中度至重度持续性IgE介导的哮喘的猫过敏患者的病情加重和减轻症状,改善了哮喘控制。

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