Benralizumab Reduces Respiratory Exacerbations and Oral Glucocorticosteroid Dose in Patients with Severe Asthma and Eosinophilic Granulomatosis with Polyangiitis.

IF 3.7 3区 医学 Q2 ALLERGY
Journal of Asthma and Allergy Pub Date : 2024-06-06 eCollection Date: 2024-01-01 DOI:10.2147/JAA.S461800
Carlo Mümmler, Pontus Mertsch, Michaela Barnikel, Frank Haubner, Ulf Schönermarck, Ulrich Grabmaier, Hendrik Schulze-Koops, Jürgen Behr, Nikolaus Kneidinger, Katrin Milger
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引用次数: 0

Abstract

Background: Benralizumab reduces exacerbations and long-term oral glucocorticosteroid (OCS) exposure in patients with severe eosinophilic asthma. In patients with eosinophilic granulomatosis with polyangiitis (EGPA), uncontrolled symptoms and exacerbations of asthma and chronic rhinosinusitis (CRS) are important reasons for continued OCS therapies. We aimed to describe outcomes of patients with severe asthma and EGPA treated with benralizumab in real-life.

Methods: We retrospectively analyzed adult patients from the Severe Asthma Unit at LMU Munich diagnosed with severe asthma and EGPA treated with benralizumab, differentiating two groups: Group A, patients with a stable daily OCS dose and diagnosis of EGPA >6 months ago; and Group B, patients treated with high-dose daily OCS due to recent diagnosis of EGPA <6 months ago. We compared outcome parameters at baseline and 12 months after initiation of benralizumab, including respiratory exacerbations, daily OCS dose, and lung function.

Results: Group A included 17 patients, all receiving OCS therapy and additional immunosuppressants; 15 patients (88%) continued benralizumab for more than 12 months, demonstrating a significant reduction in daily OCS dose and exacerbations while FEV1 increased. Group B included 9 patients, all with high-dose daily OCS and some receiving cyclophosphamide pulse therapy for life-threatening disease. Benralizumab addition during induction was well tolerated. A total of 7/9 (78%) continued benralizumab for more than 12 months and preserved EGPA remission at the 12-month timepoint.

Conclusion: In this real-life cohort of patients with severe asthma and EGPA, benralizumab initiation during remission maintenance reduced respiratory exacerbations and daily OCS dose. Benralizumab initiation during remission induction was associated with a high rate of clinical EGPA remission.

本拉珠单抗可减少重症哮喘和多发性炎性嗜酸性粒细胞增多症患者的呼吸道症状加重和口服糖皮质激素剂量
背景本拉珠单抗可减少严重嗜酸性粒细胞性哮喘患者的病情加重和长期口服糖皮质激素(OCS)的机会。在嗜酸性粒细胞肉芽肿伴多血管炎(EGPA)患者中,哮喘和慢性鼻窦炎(CRS)的症状无法控制和加重是继续接受 OCS 治疗的重要原因。我们旨在描述严重哮喘和 EGPA 患者接受苯拉利珠单抗治疗后的实际疗效:我们回顾性地分析了慕尼黑医科大学重症哮喘病房的成年患者,这些患者被诊断为重症哮喘和接受苯拉利珠单抗治疗的 EGPA 患者,分为两组:A组:每日OCS剂量稳定且6个月前诊断出EGPA的患者;B组:因最近诊断出EGPA而接受大剂量每日OCS治疗的患者:A 组包括 17 名患者,所有患者都接受了 OCS 治疗和额外的免疫抑制剂;15 名患者(88%)继续使用苯拉利珠单抗超过 12 个月,结果显示每日 OCS 剂量和病情加重次数显著减少,同时 FEV1 增加。B 组包括 9 名患者,他们都接受了大剂量的每日 OCS,其中一些患者因危及生命而接受了环磷酰胺脉冲治疗。在诱导期间加用 Benralizumab 的耐受性良好。7/9的患者(78%)继续使用苯拉利珠单抗超过12个月,并在12个月的时间点上保持了EGPA缓解:结论:在这批重症哮喘和 EGPA 患者中,在维持缓解期间开始使用贝那利珠单抗可减少呼吸道症状加重和每日 OCS 剂量。在缓解诱导期间使用苯拉利珠单抗与 EGPA 临床缓解率高有关。
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来源期刊
Journal of Asthma and Allergy
Journal of Asthma and Allergy Medicine-Immunology and Allergy
CiteScore
5.30
自引率
6.20%
发文量
185
审稿时长
16 weeks
期刊介绍: An international, peer-reviewed journal publishing original research, reports, editorials and commentaries on the following topics: Asthma; Pulmonary physiology; Asthma related clinical health; Clinical immunology and the immunological basis of disease; Pharmacological interventions and new therapies. Although the main focus of the journal will be to publish research and clinical results in humans, preclinical, animal and in vitro studies will be published where they shed light on disease processes and potential new therapies.
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