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美泊利珠单抗和贝那利珠单抗治疗嗜酸性粒细胞性哮喘的比较疗效

The Comparative Effectiveness of Mepolizumab and Benralizumab in the Treatment of Eosinophilic Asthma.

作者信息

Niemiec-Górska Aleksandra, Branicka Olga, Olszewska Paula, Mielcarska Sylwia, Glück Joanna, Rymarczyk Barbara, Gawlik Radosław

机构信息

Department of Internal Medicine, Allergology and Clinical Immunology, Faculty of Medical Sciences in Zabrze, Medical University of Silesia, 40-752 Katowice, Poland.

Doctoral School, Medical University of Silesia, 40-752 Katowice, Poland.

出版信息

Adv Respir Med. 2025 Jun 20;93(4):21. doi: 10.3390/arm93040021.

Abstract

BACKGROUND

Severe asthma is associated with significant morbidity and risk of complications. Some patients, suffering from eosinophilic asthma, may benefit from biological therapies, especially anti IL-5 (anti-interleukin-5). The purpose of the study was to compare the efficacy evaluation of mepolizumab and benralizumab in the treatment of eosinophilic asthma.

METHODS

A retrospective, single-centre study including 59 patients with severe eosinophilic asthma treated with biologics (mepolizumab and benralizumab). Clinical outcomes, including peripheral blood morphotic characteristics, spirometry parameters, asthma control questionnaire (ACQ), mini-Asthma Quality of Life Questionnaire (mini-AQLQ) scores, daily oral corticosteroid use, body mass index, exacerbation rate, and exercise tolerance, were examined at the beginning and after 6 months of biological treatment.

RESULTS

A total of 38 patients were treated with mepolizumab and 21 with benralizumab. Significant improvements ( < 0.05) in eosinophil count, required daily dose of glucocorticoids, ACQ, mini-AQLQ scores, and exacerbation rate were observed in both groups after six months of treatment. There was no statistical difference ( < 0.05) in the abovementioned parameters between the groups.

CONCLUSIONS

In patients with severe eosinophilic asthma, mepolizumab and benralizumab were associated with significant improvements in clinical state. Patients with type 2 asthma will benefit from the therapy with both anti-IL5 biologic drugs.

摘要

背景

重度哮喘与显著的发病率和并发症风险相关。一些患有嗜酸性粒细胞性哮喘的患者可能从生物治疗中获益,尤其是抗白细胞介素-5(抗IL-5)治疗。本研究的目的是比较美泊利珠单抗和贝那利珠单抗治疗嗜酸性粒细胞性哮喘的疗效评估。

方法

一项回顾性单中心研究,纳入59例接受生物制剂(美泊利珠单抗和贝那利珠单抗)治疗的重度嗜酸性粒细胞性哮喘患者。在生物治疗开始时和治疗6个月后,检查临床结局,包括外周血形态学特征、肺功能参数、哮喘控制问卷(ACQ)、小型哮喘生活质量问卷(mini-AQLQ)评分、每日口服糖皮质激素用量、体重指数、加重率和运动耐量。

结果

共有38例患者接受美泊利珠单抗治疗,21例接受贝那利珠单抗治疗。治疗6个月后,两组患者的嗜酸性粒细胞计数、每日所需糖皮质激素剂量、ACQ、mini-AQLQ评分和加重率均有显著改善(<0.05)。两组上述参数之间无统计学差异(<0.05)。

结论

在重度嗜酸性粒细胞性哮喘患者中,美泊利珠单抗和贝那利珠单抗均与临床状态的显著改善相关。2型哮喘患者将从两种抗IL-5生物药物治疗中获益。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/94e5/12382853/d07dbf54a179/arm-93-00021-g001.jpg

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