Effective long-term prophylaxis with lanadelumab in adolescents with hereditary angioedema: EMPOWER/ENABLE.

IF 4.3 2区 医学 Q2 ALLERGY
Raffi Tachdjian, Aleena Banerji, Paula J Busse, Nancy Agmon-Levin, John Anderson, Mauro Cancian, Giuseppe Spadaro, Carmen Enciu, Daniel Nova Estepan, Natalie Khutoryansky, Siddharth Jain, Andreas Recke
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引用次数: 0

Abstract

Background: Symptoms of hereditary angioedema (HAE) typically first present during childhood, but the frequency/severity of attacks often increases at puberty. Real-world data on long-term HAE prophylaxis in adolescents are limited. We report pooled data from adolescent patients enrolled in two Phase 4 studies (EMPOWER, ENABLE) evaluating the effectiveness/safety of lanadelumab (monoclonal antibody directed against plasma kallikrein) for the prevention of HAE attacks.

Methods: Adolescent patients (aged 12 to <18 years) with HAE-C1INH enrolled in EMPOWER and ENABLE received open-label lanadelumab 300 mg once every 2 weeks. Effectiveness outcomes were based on patient-reported assessments of on-treatment HAE attacks. Safety was assessed through the recording of treatment-emergent adverse events (TEAEs) and serious adverse events. This analysis categorized patients as "new" or "established" lanadelumab patients.

Results: Thirteen new and seven established patients on lanadelumab were included. The observed monthly attack rate in new patients fell from 3.8 (mean) and 2.8 (median) during the pre-enrollment period to 0.65 (mean) and 0.21 (median) during the cumulative study period after lanadelumab initiation (84.2% and 92.9% reductions, respectively). In established patients, mean (SD) HAE attack rate (as treated) during the overall study period was 0.04 (0.03) attacks/month. Most HAE attacks were of mild/moderate severity. Nine new patients reported 42 TEAEs, mostly mild/moderate in severity, with 3 TEAEs reported as serious. Seven established patients reported 12 TEAEs (all mild/moderate and non-serious). No TEAEs were related to lanadelumab.

Conclusion: These data support lanadelumab's effectiveness/safety in adolescents with HAE, consistent with results from Phase 3 lanadelumab studies in mixed adult/adolescent populations.

Clinical trial identifiers: NCT03845400 (EMPOWER) and NCT04130191 (ENABLE).

lanadelumab对青少年遗传性血管性水肿的有效长期预防:EMPOWER/ENABLE
背景:遗传性血管性水肿(HAE)的症状通常在儿童期首次出现,但发作的频率/严重程度通常在青春期增加。青少年长期HAE预防的实际数据是有限的。我们报告了来自两项4期研究(EMPOWER, ENABLE)的青少年患者的汇总数据,该研究评估了lanadelumab(针对血浆激肽肽的单克隆抗体)预防HAE发作的有效性和安全性。方法:青少年患者(12岁至12岁)。结果:纳入了13例新患者和7例已建立的lanadelumab患者。观察到新患者的月发作率从入组前的3.8(平均)和2.8(中位数)下降到lanadelumab开始后的累积研究期间的0.65(平均)和0.21(中位数)(分别下降84.2%和92.9%)。在确定的患者中,在整个研究期间,平均(SD) HAE发作率(治疗时)为0.04(0.03)次/月。大多数HAE发作的严重程度为轻/中度。9例新患者报告了42例teae,大多数为轻度/中度严重,其中3例报告为严重teae。7例确诊患者报告了12例teae(均为轻/中度和非严重)。没有teae与lanadelumab相关。结论:这些数据支持lanadelumab在青少年HAE患者中的有效性/安全性,与lanadelumab在成人/青少年混合人群中的3期研究结果一致。临床试验标识符:NCT03845400 (EMPOWER)和NCT04130191 (ENABLE)。
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来源期刊
CiteScore
9.10
自引率
9.10%
发文量
200
审稿时长
4-8 weeks
期刊介绍: Pediatric Allergy and Immunology is the world''s leading journal in pediatric allergy, publishing original contributions and comprehensive reviews related to the understanding and treatment of immune deficiency and allergic inflammatory and infectious diseases in children. Other areas of interest include: development of specific and accessory immunity; the immunological interaction during pregnancy and lactation between mother and child. As Pediatric Allergy and Immunology promotes communication between scientists engaged in basic research and clinicians working with children, we publish both clinical and experimental work.
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