Magerl Markus, Bouillet Laurence, Martinez-Saguer Inmaculada, Gavini Francois, Bent-Ennakhil Nawal, Sayegh Laura, Andresen Irmgard
Institute of Allergology, Charité - Universitätsmedizin Berlin and Fraunhofer Institute for Translational Medicine and Pharmacology ITMP, Immunology and Allergology, Berlin, Germany.
Department of Internal Medicine, National Reference Centre for Angioedema (CREAK), Université Grenoble Alpes, Grenoble, France.
J Allergy Clin Immunol Pract. 2025 Feb;13(2):378-387.e2. doi: 10.1016/j.jaip.2024.12.008. Epub 2024 Dec 17.
Hereditary angioedema (HAE) is a rare genetic disease characterized by recurrent episodes of cutaneous or subcutaneous edema. There is clinical need for treatments that reduce the rate of HAE attacks in patients.
Primary objectives were to evaluate the effectiveness of lanadelumab on attack-free rate (AFR; proportion of patients who had zero HAE attacks), and of every 2-week and every 4-week adjustments on AFR.
A retrospective medical chart review study was conducted in 19 HAE centers and included data from patients with type I or II HAE treated with lanadelumab (index treatment) in Germany, France, Greece, and Austria who were aged 12 years or older (ClinicalTrials.gov identifier: NCT04861090). Data abstraction occurred September 15, 2021, to June 29, 2022. Analyses were primarily descriptive.
Data from 198 patients were collected (61.6% female, 91.9% with type I HAE). Lanadelumab treatment patterns varied between countries. Cumulative AFR improved from 0% (preindex) to 54.4% (12 months postindex) and 39.4% (postindex; median duration, 28.8 months). Monthly AFRs varied from 16.2% to 28.3% preindex (17.7% AFR in the month before index date), and from 82.7% (month 1) to more than 95% at multiple time points between 26 and 43 months postindex. Patients with interval increases (n = 144 [72.7%]) showed improved cumulative AFR (0% preindex to 50.0% postindex).
This real-world study demonstrates that lanadelumab long-term prophylaxis is effective in improving AFR in patients with type I/II HAE on every 2-week dosing and dose interval increases. Effectiveness with lanadelumab is rapid and was observed starting from the first month of starting therapy.
遗传性血管性水肿(HAE)是一种罕见的遗传性疾病,其特征为皮肤或皮下水肿反复发作。临床上需要能够降低HAE患者发作率的治疗方法。
主要目的是评估拉那度单抗对无发作率(AFR;HAE发作次数为零的患者比例)的有效性,以及每2周和每4周调整剂量对AFR的影响。
在19个HAE中心进行了一项回顾性病历审查研究,纳入了德国、法国、希腊和奥地利12岁及以上接受拉那度单抗(索引治疗)治疗的I型或II型HAE患者的数据(ClinicalTrials.gov标识符:NCT04861090)。数据提取时间为2021年9月15日至2022年6月29日。分析主要为描述性分析。
收集了198例患者的数据(61.6%为女性,91.9%为I型HAE)。各国的拉那度单抗治疗模式有所不同。累积AFR从0%(索引前)提高到54.4%(索引后12个月)和39.4%(索引后;中位持续时间,28.8个月)。索引前每月AFR在16.2%至28.3%之间(索引日期前一个月的AFR为17.7%),索引后26至43个月的多个时间点,AFR从82.7%(第1个月)到超过95%不等。间隔期增加剂量的患者(n = 144 [72.7%])累积AFR有所改善(索引前为0%,索引后为50.0%)。
这项真实世界研究表明,拉那度单抗长期预防对改善I/II型HAE患者每2周给药及增加剂量间隔期的AFR有效。拉那度单抗的有效性迅速,从开始治疗的第一个月就可观察到。