Very long-term data on patients with severe eosinophilic asthma treated with mepolizumab: a case series.

Q2 Pharmacology, Toxicology and Pharmaceutics Drugs in Context Pub Date : 2024-07-22 eCollection Date: 2024-01-01 DOI:10.7573/dic.2024-4-2
Carlo Lombardi, Francesco Menzella, Alvise Berti
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Abstract

Background: Patients with severe asthma are often dependent on oral corticosteroids (OCS) and have frequent exacerbations. This article aims to report very long-term data of patients with severe eosinophilic asthma assessing asthma control, lung function, inhaled corticosteroid (ICS) dose reduction, and clinical and biological parameters of patients treated with mepolizumab.

Methods: Four cases of adult patients with severe eosinophilic asthma who were treated for 60 months or more with mepolizumab 100 mg/4 weeks, leading to the stable discontinuation of OCS, are presented. ICS dose, OCS dose and withdrawal date, lung function, eosinophil count, fractional exhaled nitric oxide, and asthma control test were recorded as well as exacerbations in the 12 months before commencing mepolizumab and in the 12 months before the last follow-up visit.

Results: Three of the patients were men, median age was 52.5 years (range 79-53), median length of asthma before mepolizumab start was 67.5 months (range 24-240), three had chronic rhinosinusitis without nasal polyposis and two were atopic. All had eosinophil counts >300 cells/μL at baseline. The median follow-up was 73.5 months (range 71-74), and OCS withdrawal from baseline occurred after a median of 13 months of mepolizumab treatment (range 12-39). A substantial reduction of ICS treatment was registered as well as improvement in asthma control test, fractional exhaled nitric oxide and functional parameters, and a significant reduction of exacerbations in the last 12 months before last visit was observed as compared to the 12 months before baseline (from a median of 4 (range 3-6) to 0; p=0.0286).

Conclusions: Mepolizumab could be a 'disease-modifying' agent, with high tolerability and a good efficacy profile in the long term.

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嗜酸性粒细胞严重哮喘患者接受甲泼尼单抗治疗的长期数据:病例系列。
背景:重症哮喘患者通常依赖口服皮质类固醇(OCS),且病情经常加重。本文旨在报告严重嗜酸性粒细胞性哮喘患者的长期数据,评估哮喘控制情况、肺功能、吸入皮质类固醇(ICS)剂量减少情况以及使用甲泼尼单抗治疗患者的临床和生物学参数:本文介绍了四例成年重度嗜酸性粒细胞哮喘患者,这些患者接受了长达 60 个月或更长时间的美泊珠单抗 100 毫克/4 周治疗,从而稳定地停用了 OCS。研究记录了ICS剂量、OCS剂量和停药日期、肺功能、嗜酸性粒细胞计数、呼出一氧化氮分数、哮喘控制测试以及开始使用甲泼尼珠单抗前12个月和最后一次随访前12个月的病情加重情况:其中三名患者为男性,年龄中位数为 52.5 岁(79-53 岁不等),开始使用甲泼尼单抗前的哮喘病期中位数为 67.5 个月(24-240 个月不),三名患者患有慢性鼻炎,但无鼻息肉病,两名患者为特应性哮喘。基线时,所有患者的嗜酸性粒细胞计数均大于 300 cells/μL。中位随访时间为 73.5 个月(71-74 个月),从基线开始停用 OCS 的时间中位数是在美泊珠单抗治疗 13 个月后(12-39 个月)。与基线前12个月相比,最后一次就诊前12个月的病情恶化显著减少(从中位数4次(3-6次)减少到0次;P=0.0286):结论:美博利珠单抗可作为一种 "疾病修饰 "药物,具有较高的耐受性和良好的长期疗效。
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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来源期刊
Drugs in Context
Drugs in Context Medicine-Medicine (all)
CiteScore
5.90
自引率
0.00%
发文量
63
审稿时长
9 weeks
期刊介绍: Covers all phases of original research: laboratory, animal and human/clinical studies, health economics and outcomes research, and postmarketing studies. Original research that shows positive or negative results are welcomed. Invited review articles may cover single-drug reviews, drug class reviews, latest advances in drug therapy, therapeutic-area reviews, place-in-therapy reviews, new pathways and classes of drugs. In addition, systematic reviews and meta-analyses are welcomed and may be published as original research if performed per accepted guidelines. Editorials of key topics and issues in drugs and therapeutics are welcomed. The Editor-in-Chief will also consider manuscripts of interest in areas such as technologies that support diagnosis, assessment and treatment. EQUATOR Network reporting guidelines should be followed for each article type. GPP3 Guidelines should be followed for any industry-sponsored manuscripts. Other Editorial sections may include Editorial, Case Report, Conference Report, Letter-to-the-Editor, Educational Section.
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