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在C1酯酶抑制剂正常的遗传性血管性水肿患者中使用贝罗司他的临床经验:病例系列评论

Clinical Experience with Berotralstat in Patients with Hereditary Angioedema with Normal C1-Esterase Inhibitor: A Commented Case Series.

作者信息

Kanarek Henry J, Mutschelknaus Drew Austin Saville

机构信息

Kanarek Allergy, Asthma & Immunology, Leawood, KS, USA.

出版信息

J Asthma Allergy. 2024 Feb 23;17:123-132. doi: 10.2147/JAA.S445893. eCollection 2024.

Abstract

Hereditary angioedema (HAE) is a rare genetic disorder characterized by potentially life-threatening episodes of swelling. Most HAE cases are caused by deficient (type I) or dysfunctional (type II) C1-esterase inhibitor (C1-INH) protein. However, some patients present with a subtype of HAE that is associated with normal plasma levels of functional C1-INH protein and complement component 4 (HAE-nC1INH). Treatment of HAE-nC1INH is driven by clinical experience as robust clinical trial data to inform treatment decisions are lacking in this population. This retrospective case series assessed clinical features and treatment outcomes in 15 patients with HAE-nC1INH who initiated long-term prophylaxis with oral berotralstat 150 mg once daily as part of their disease management pathway. Most patients were female (93%), with a median age of 49 years. All patients experienced abdominal swelling attacks. On average, patients tried a mean of 4 different treatments for their HAE, including berotralstat. Although most patients associated prophylactic and on-demand medications that target the bradykinin pathway with improvements in the frequency and/or severity of attacks, treatment outcomes varied considerably between patients, highlighting the importance of a personalized approach to disease management. In this case series, berotralstat was an effective prophylactic treatment option in most patients with HAE-nC1INH. Further studies are required to demonstrate the potential efficacy, safety, and impact on quality of life of currently approved HAE therapies in patients with HAE-nC1INH.

摘要

遗传性血管性水肿(HAE)是一种罕见的遗传性疾病,其特征是可能危及生命的肿胀发作。大多数HAE病例是由C1酯酶抑制剂(C1-INH)蛋白缺乏(I型)或功能失调(II型)引起的。然而,一些患者表现为HAE的一种亚型,其血浆中功能性C1-INH蛋白和补体成分4水平正常(HAE-nC1INH)。由于缺乏有力的临床试验数据来指导治疗决策,HAE-nC1INH的治疗主要基于临床经验。本回顾性病例系列评估了15例HAE-nC1INH患者的临床特征和治疗结果,这些患者开始接受口服贝拉他司特150mg每日一次的长期预防治疗,作为其疾病管理途径的一部分。大多数患者为女性(93%),中位年龄为49岁。所有患者均经历过腹部肿胀发作。平均而言,患者针对其HAE尝试过平均4种不同的治疗方法,包括贝拉他司特。尽管大多数患者将针对缓激肽途径的预防性和按需用药与发作频率和/或严重程度的改善相关联,但患者之间的治疗结果差异很大,突出了个性化疾病管理方法的重要性。在本病例系列中,贝拉他司特对大多数HAE-nC1INH患者是一种有效的预防性治疗选择。需要进一步研究来证明目前批准的HAE疗法对HAE-nC1INH患者的潜在疗效、安全性和对生活质量的影响。

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