Guy's Severe Asthma Centre, Guy's & St Thomas' NHS Trust, London, United Kingdom; Asthma UK Centre, School of Immunology & Microbial Sciences, King's College London, London, United Kingdom.
Royal Liverpool and Broadgreen University Hospitals NHS Trust, Liverpool, United Kingdom.
J Allergy Clin Immunol Pract. 2022 Jun;10(6):1534-1544.e4. doi: 10.1016/j.jaip.2022.02.014. Epub 2022 Feb 22.
Benralizumab is an IL-5 receptor alpha-directed cytolytic mAb that depletes eosinophils, reducing exacerbations and oral corticosteroid (OCS) use, and improves asthma control for patients with severe eosinophilic asthma (SEA). Data on response in patients previously treated with other biologic therapies are limited.
To describe real-world clinical outcomes with benralizumab for patients with and without prior biologic use for uncontrolled SEA.
This retrospective study compared clinical outcomes before and after benralizumab initiation in adults with uncontrolled SEA with 3 or more asthma exacerbations in the previous 12 months or on maintenance OCS treatment. Outcomes included exacerbations, OCS use, patient-reported outcomes, and health care resource utilization, including emergency department visits and hospitalizations.
In all, 208 patients were enrolled, including 90 (43.3%) with previous experience with an alternate biologic for SEA. Benralizumab led to an 81% reduction in exacerbation rate, with 48% of patients with previous exacerbations experiencing none after 48 weeks. Overall, 67% of patients requiring baseline maintenance OCS achieved greater than or equal to 50% reduction in daily OCS dosage, and 53% eliminated maintenance OCS. Clinically meaningful improvements in patient-reported outcomes were seen, with response at 4 weeks predicting longer-term benefits. Health care resource utilization also decreased. Improvements were observed irrespective of previous biologic experience, fractional exhaled nitric oxide concentrations, atopic status, or other baseline characteristics.
In a multicenter real-world setting, patients with uncontrolled SEA achieved substantial improvements in all clinical outcome measures with benralizumab irrespective of previous biologic use, atopic status, or baseline fractional exhaled nitric oxide concentration.
贝那鲁肽是一种靶向白细胞介素-5 受体 α 的细胞溶解单克隆抗体,可消耗嗜酸性粒细胞,减少加重和口服皮质类固醇(OCS)的使用,并改善重度嗜酸性粒细胞性哮喘(SEA)患者的哮喘控制。关于先前接受其他生物治疗患者的反应数据有限。
描述贝那鲁肽治疗先前接受和未接受生物治疗的控制不佳的 SEA 患者的真实世界临床结局。
本回顾性研究比较了在过去 12 个月内有 3 次或更多哮喘加重或正在接受维持 OCS 治疗的控制不佳的 SEA 成年患者在开始贝那鲁肽治疗前后的临床结局。结局包括加重、OCS 使用、患者报告的结局以及包括急诊就诊和住院在内的卫生保健资源利用情况。
共纳入 208 例患者,其中 90 例(43.3%)先前有 SEA 的替代生物治疗经验。贝那鲁肽使加重率降低了 81%,48 周后有先前加重史的患者中有 48%无加重。总体而言,67%需要基线维持 OCS 的患者实现了每日 OCS 剂量减少≥50%,53%消除了维持 OCS。患者报告的结局也有明显的改善,4 周时的反应预测了更长期的获益。卫生保健资源利用也减少了。无论先前的生物治疗经验、呼出气一氧化氮分数、特应性状态或其他基线特征如何,均观察到改善。
在多中心真实世界环境中,控制不佳的 SEA 患者无论先前是否使用生物制剂、特应性状态或基线呼出气一氧化氮分数如何,使用贝那鲁肽均可在所有临床结局指标上均获得显著改善。