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重度哮喘有可能实现缓解吗?对接受美泊利珠单抗治疗的真实队列中四年反应的回顾性分析。

Is it possible to achieve remission in severe asthma? Retrospective analysis of a four-year response in a real-life cohort treated with mepolizumab.

作者信息

Correa-Borit Jorge, Laorden Daniel, Arnalich Montiel Victoria, Quirce Santiago, Domínguez-Ortega Javier

机构信息

Department of Allergy, Hospital La Paz, Madrid, Spain.

Department of Pneumology, Hospital La Paz, Madrid, Spain.

出版信息

J Asthma. 2025 May;62(5):794-797. doi: 10.1080/02770903.2024.2441887. Epub 2025 Jan 2.

DOI:10.1080/02770903.2024.2441887
PMID:39661869
Abstract

Response to biologics in severe uncontrolled asthma (SUA) can be classified as super-responders, good responders, non-responders, and those achieving clinical remission. The aim of this study is to evaluate the long-term response to mepolizumab in patients with severe eosinophilic asthma and assesses the rate of asthma clinical remission over four years in a real-life setting. This is a single-center, observational, retrospective study was conducted at La Paz University Hospital (Madrid, Spain) from 2017 to 2022. Patients with SUA treated with mepolizumab 100mg every four weeks for at least three years were included. Response to mepolizumab was classified into good responders, super-responders, non-responders, and patients achieving clinical remission after three and four years of treatment. 27 patients (67% women; mean age 37.7 years) were included. 58% of patients achieved remission after three years of treatment, increasing to 63% after four years. Similar trends were observed in super-responders and good responders. We found that a significant number of patients treated with mepolizumab in a real-life setting can achieve asthma remission, particularly when compared to other similar studies. By distinguishing these different degrees of response, clinicians can better understand the patient's condition and make more informed decisions about whether to continue with the current biologic therapy or consider switching to a different treatment.

摘要

重度未控制哮喘(SUA)对生物制剂的反应可分为超反应者、良好反应者、无反应者以及实现临床缓解者。本研究的目的是评估重度嗜酸性粒细胞性哮喘患者对美泊利珠单抗的长期反应,并在现实环境中评估四年内哮喘临床缓解率。这是一项于2017年至2022年在西班牙马德里拉巴斯大学医院开展的单中心、观察性、回顾性研究。纳入每四周接受100mg美泊利珠单抗治疗至少三年的SUA患者。将美泊利珠单抗的反应分为良好反应者、超反应者、无反应者以及治疗三年和四年后实现临床缓解的患者。共纳入27例患者(67%为女性;平均年龄37.7岁)。58%的患者在治疗三年后实现缓解,四年后这一比例增至63%。超反应者和良好反应者也观察到类似趋势。我们发现,在现实环境中接受美泊利珠单抗治疗的大量患者可实现哮喘缓解,特别是与其他类似研究相比。通过区分这些不同程度的反应,临床医生可以更好地了解患者病情,并就是否继续当前生物制剂治疗或考虑换用不同治疗做出更明智的决策。

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