Institute of Allergology, Charité - Universitätsmedizin Berlin, Corporate Member of Freie Universität Berlin and Humboldt-Universität zu Berlin, Berlin, Germany.
Fraunhofer Institute for Translational Medicine and Pharmacology ITMP, Immunology and Allergology, Berlin, Germany.
Front Immunol. 2024 May 10;15:1405317. doi: 10.3389/fimmu.2024.1405317. eCollection 2024.
Lanadelumab is a first-line long-term prophylaxis (LTP) in hereditary angioedema (HAE). Real-life data on its long-term efficacy and safety are limited. It is unknown whether patients using lanadelumab need short-term prophylaxis (STP).
To provide 4-year follow-up data for our first 34 patients treating with lanadelumab.
Patients were assessed for their current injection interval, attacks, treatment satisfaction, disease control (AECT), quality of life impairment (AE-QoL), events that can induce attacks, and the use of STP since the start of their treatment with lanadelumab.
Of 34 patients who started lanadelumab treatment, 32 were still using it after 4 years, with a median injection interval of 33 (range 14-90) days. HAE patients (n=28) reported longer intervals, i.e. 35 (14-90) days, than patients with angioedema due to acquired C1 inhibitor deficiency (n=4, 23 (14-31) days). With their current injection intervals, used for a mean duration of 29 ± 17 months, patients reported a yearly attack rate of 0.3 ± 0.1. More than 70% of patients were attack-free since starting their current injection interval. All patients reported well-controlled disease, i.e. ≥10 points in the AECT; 21 patients had complete control (16 points). AE-QoL scores improved further compared to our initial report, most prominently in the fears/shame domain (-6 points). Treatment satisfaction was very high. No angioedema occurred after 146 of 147 potentially attack-inducing medical procedures without STP.
Our results demonstrate the long-term efficacy and safety of lanadelumab in real-life and question the need for STP in patients who use effective LTP.
拉那芦单抗是遗传性血管水肿(HAE)的一线长期预防(LTP)药物。关于其长期疗效和安全性的真实数据有限。目前尚不清楚使用拉那芦单抗的患者是否需要短期预防(STP)。
为前 34 名接受拉那芦单抗治疗的患者提供 4 年随访数据。
评估患者目前的注射间隔、发作次数、治疗满意度、疾病控制(AECT)、生活质量受损(AE-QoL)、可能引发发作的事件以及自开始接受拉那芦单抗治疗以来使用 STP 的情况。
34 名开始接受拉那芦单抗治疗的患者中有 32 名在 4 年后仍在使用该药,中位注射间隔为 33(14-90)天。HAE 患者(n=28)报告的间隔时间较长,即 35(14-90)天,而获得性 C1 抑制剂缺乏症引起的血管水肿患者(n=4,23(14-31)天)。根据他们目前的注射间隔,平均使用 29±17 个月,患者报告的年发作率为 0.3±0.1。自开始当前注射间隔以来,超过 70%的患者无发作。所有患者报告疾病得到很好的控制,即 AECT 得分为≥10 分;21 名患者完全控制(16 分)。与我们最初的报告相比,AE-QoL 评分进一步改善,特别是在恐惧/羞耻领域(-6 分)。治疗满意度非常高。在没有 STP 的情况下,147 次潜在诱发发作的医疗程序中有 146 次未发生血管水肿。
我们的结果表明,拉那芦单抗在真实世界中具有长期疗效和安全性,并质疑使用有效 LTP 的患者是否需要 STP。