Becoming attack-free further improves health-related quality of life in patients with hereditary angioedema receiving garadacimab.

IF 2.6 3区 医学 Q2 ALLERGY
Petra Staubach, Timothy J Craig, Tomoo Fukuda, Emel Aygoren-Pursun, Roman Hakl, Julia Braverman, John-Philip Lawo, Maressa Pollen, Chiara Nenci, Philip H Li, Henriette Farkas
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引用次数: 0

Abstract

Background: Hereditary angioedema (HAE) is associated with substantial health-related quality of life (HRQoL) impairments. Complete disease control and life normalization are key treatment goals. In previous studies, garadacimab prevented HAE attacks with a favorable safety profile and HRQoL improvements. Objective: HRQoL was evaluated in patients with HAE receiving garadacimab stratified by attack-free status. Methods: In the pivotal phase III study (NCT04656418), 39 patients received garadacimab 200 mg subcutaneously once monthly and 25 volume-matched placebo. In the phase III open-label extension (OLE), 90 patients in the garadacimab-naive group (received placebo in previous studies or newly enrolled) and 71 patients in the previous garadacimab exposure group (received garadacimab in previous studies) received garadacimab (NCT04739059). Patients ages ≥ 18 years completed the Angioedema Quality of Life (AE-QoL) questionnaire in both studies; scores were evaluated post hoc by attack-free status. Results: In the pivotal phase III and phase III OLE studies, 62% and 60% of patients, respectively, were attack-free. In the pivotal phase III study, the mean AE-QoL total score improved with garadacimab, from 38.8 (day 1) to 6.6 (month 6) for attack-free patients (n = 19) and to 18.4 for patients with one or more attacks (n = 14) versus a change in mean AE-QoL total score from 43.7 to 40.5 with placebo (n = 20). In the phase III OLE study, the mean AE-QoL total score for patients who were garadacimab naive decreased from 46.2 (day 1) to 8.6 (month 12) for attack-free patients (n = 34) and from 54.5 to 23.5 for patients with one or more attacks (n = 30). For the previous garadacimab exposure group, AE-QoL improvements were maintained from previous studies, regardless of attack-free status. Conclusion: Garadacimab was associated with HRQoL improvement versus run-in in all groups. After garadacimab exposure in previous studies, improvements were maintained in the phase III OLE study. Attack-free patients had the greatest HRQoL improvements, bringing them closer to complete disease control and life normalization.Clinical trials NCT04656418, NCT04739059, www.clinicaltrials.gov.

无发作进一步改善了接受加达西单抗治疗的遗传性血管性水肿患者的健康相关生活质量。
背景:遗传性血管性水肿(HAE)与健康相关的生活质量(HRQoL)损害相关。疾病完全控制和生活正常化是治疗的主要目标。在先前的研究中,garadacimab预防HAE发作,具有良好的安全性和HRQoL改善。目的:评价接受加达西单抗治疗的HAE患者的HRQoL,并按无发作状态分层。方法:在关键的III期研究(NCT04656418)中,39例患者每月接受一次加达西单抗200mg皮下注射和25例容量匹配的安慰剂。在III期开放标签扩展(OLE)试验中,90例garadacimab初始组(在既往研究中接受安慰剂或新入组)和71例garadacimab暴露组(在既往研究中接受garadacimab)患者接受了garadacimab (NCT04739059)。两项研究中年龄≥18岁的患者均完成了血管性水肿生活质量(AE-QoL)问卷调查;通过事后无攻击状态评估得分。结果:在关键的III期和III期OLE研究中,分别有62%和60%的患者无发作。在关键的III期研究中,garadacimab组的AE-QoL平均总分从无发作患者(n = 19)的38.8(第1天)提高到6.6(第6个月),有一次或多次发作患者(n = 14)的AE-QoL平均总分从43.7提高到40.5,而安慰剂组的AE-QoL平均总分从43.7提高到40.5 (n = 20)。在III期OLE研究中,无发作患者(n = 34)未经garadacimab治疗的AE-QoL平均总分从46.2(第1天)降至8.6(第12个月),有一次或多次发作的患者(n = 30)从54.5降至23.5。对于先前的garadacimab暴露组,AE-QoL的改善与先前的研究相比保持不变,无论无发作状态如何。结论:加拉达昔单抗与各组HRQoL改善相关。在先前的研究中暴露于garadacimab后,在III期OLE研究中保持了改善。无发作患者的HRQoL改善最大,使其更接近完全疾病控制和生活正常化。临床试验NCT04656418, NCT04739059, www.clinicaltrials.gov。
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来源期刊
CiteScore
5.70
自引率
35.70%
发文量
106
审稿时长
6-12 weeks
期刊介绍: Allergy & Asthma Proceedings is a peer reviewed publication dedicated to distributing timely scientific research regarding advancements in the knowledge and practice of allergy, asthma and immunology. Its primary readership consists of allergists and pulmonologists. The goal of the Proceedings is to publish articles with a predominantly clinical focus which directly impact quality of care for patients with allergic disease and asthma. Featured topics include asthma, rhinitis, sinusitis, food allergies, allergic skin diseases, diagnostic techniques, allergens, and treatment modalities. Published material includes peer-reviewed original research, clinical trials and review articles.
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