In search of clinically relevant parameters to monitor successful omalizumab therapy in allergic asthma.

Allergologie Select Pub Date : 2019-09-01 eCollection Date: 2018-01-01 DOI:10.5414/ALX01377E
M Probst, A Gogolka, M Krüll, O Noga
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引用次数: 6

Abstract

Background: Omalizumab is approved as add-on therapy for the treatment of severe uncontrolled allergic asthma. Increase in quality of life and decrease of exacerbations and hospital admission, as well as immunmodulatory effects have been described with omalizumab therapy. However, to date there are few parameters to monitor success and to evaluate the individual advantage of this therapy for the patient. Furthermore, no reliable parameter to predict response to treatment exists so far. The aim of this study was to define an easily applicable parameter for response to treatment with omalizumab.

Method: 43 patients with allergic asthma were treated with omalizumab at a dose of at least 0,016 mg/kg/IgE every 4 weeks. Before, and 12 weeks after initiation of therapy, bodyplethysmography including airway resistance was performed. Efficacy of treatment was judged by the attending physician on the basis of a five point chart. Furthermore, a differential blood count was performed before, and 12 weeks after initiation of treatment. Total and specific IgE against all relevant antigens were determined before start of therapy.

Results: Airway resistance in patients with response to treatment with omalizumab (responders) was significantly decreased in comparison to patients without clinical benefit (non-responder). The number of eosinophil granulocytes in the peripheral blood was decreased in both groups without significant difference. Response to therapy was associated with younger age and lower levels of specific IgE against the allergen with the highest sIgE-level (seasonal and perennial), but not with the sIgE level of the perennial allergens in general.

Conclusion: Measurement of airway resistance might be an additional parameter for monitoring response to therapy with omalizumab. High specific IgE levels, for both perennial and concomitant seasonal allergens as well as increasing age, seem to predict less favorable treatment outcomes.

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寻找临床相关参数以监测奥玛单抗治疗过敏性哮喘的成功。
背景:Omalizumab被批准作为治疗严重不受控制的过敏性哮喘的附加疗法。奥玛珠单抗治疗提高了生活质量,减少了病情恶化和住院,以及免疫调节作用。然而,迄今为止,很少有参数来监测成功和评估这种治疗对患者的个体优势。此外,到目前为止还没有可靠的参数来预测对治疗的反应。本研究的目的是定义一个容易适用的参数,以响应与奥玛珠单抗治疗。方法:43例过敏性哮喘患者采用奥玛珠单抗治疗,剂量至少为0.016 mg/kg/IgE,每4周一次。治疗开始前和治疗开始后12周,进行包括气道阻力在内的体体积脉搏波描记。治疗效果由主治医师根据五分表判断。此外,在治疗开始前和治疗开始后12周进行差异血细胞计数。治疗开始前测定所有相关抗原的总IgE和特异性IgE。结果:与无临床获益(无应答)的患者相比,对omalizumab治疗有反应的患者(应答者)的气道阻力显著降低。两组患者外周血嗜酸性粒细胞数量均减少,但差异无统计学意义。对治疗的反应与年龄较小和针对sIgE水平最高的过敏原(季节性和多年生)的特异性IgE水平较低有关,但与多年生过敏原的sIgE水平一般无关。结论:测量气道阻力可能是监测对奥玛单抗治疗反应的附加参数。对于常年和伴随的季节性过敏原以及年龄的增长,高特异性IgE水平似乎预示着不太有利的治疗结果。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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