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C1抑制剂替代疗法用于遗传性血管性水肿长期预防的随机对照试验综述:疾病症状的缓解是可以实现的。

A Review of Randomized Controlled Trials of Hereditary Angioedema Long-Term Prophylaxis with C1 Inhibitor Replacement Therapy: Alleviation of Disease Symptoms Is Achievable.

作者信息

Longhurst Hilary J, Valerieva Anna

机构信息

Department of Medicine, University of Auckland and Department of Immunology, Auckland City Hospital, Auckland, New Zealand.

Department of Allergology, Medical University of Sofia, Sofia, Bulgaria.

出版信息

J Asthma Allergy. 2023 Mar 9;16:269-277. doi: 10.2147/JAA.S396338. eCollection 2023.

Abstract

Through its fluctuating disease activity and unpredictable attacks, hereditary angioedema (HAE) imposes a substantial patient burden. To minimize HAE burden and improve quality of life, treatment should involve individualized management strategies that address on-demand therapy and short-term/long-term prophylaxis. Goals of long-term prophylaxis include reducing the number, severity, and burden of HAE attacks. The best characterized forms of HAE arise from deficiency or dysfunction of C1-inhibitor (C1-INH; types I/II), and C1-INH replacement therapy is a first-line intervention for on-demand (acute) treatment of HAE attacks, short-term prophylaxis before high-risk procedures, and long-term prophylaxis. Randomized, double-blind, placebo-controlled crossover trials have shown dose-dependent efficacy with plasma-derived C1-INH (pdC1-INH) 40-60 IU/kg subcutaneously, pdC1-INH 1000 U intravenously, and recombinant human C1-INH (rhC1-INH) 50 IU/kg (maximum 4200 IU) intravenously, all administered twice weekly, as long-term prophylaxis in patients with a history of 2 to ≥4 attacks/month. Overall, up to 83% (pdC1-INH 60 IU/kg) of patients experienced an HAE attack reduction threshold of ≥70%, and up to 58% (pdC1-INH 60 IU/kg) achieved an attack reduction threshold of ≥90%. Lower-dose intravenous pdC1-INH therapy (1000 U) was seemingly less effective, with 45% of 22 patients experiencing an HAE attack reduction threshold of ≥70%, and up to 23% achieving an attack reduction threshold of ≥90%. Higher-dose intravenous rhC1-INH 50 IU/kg (maximum, 4200 IU) twice weekly was of intermediate benefit. Despite a baseline mean attack frequency of 17.9 (during the 3 months prior to study treatment) and a mean attack frequency during a 4-week placebo period of 7.2, 52% of 23 patients experienced ≥70% reduction in attack frequency and 26% of 23 patients experienced ≥90% reduction in attack frequency. The increasing patient percentages treated with C1-INH replacement therapy as long-term prophylaxis meeting these high thresholds reinforces hopes and expectations that "attack freedom" is achievable, including for those with moderate or severe disease.

摘要

遗传性血管性水肿(HAE)因其疾病活动波动和发作不可预测,给患者带来了沉重负担。为了将HAE负担降至最低并提高生活质量,治疗应采用个性化管理策略,包括按需治疗以及短期/长期预防。长期预防的目标包括减少HAE发作的次数、严重程度和负担。最典型的HAE形式是由C1抑制剂(C1-INH;I/II型)缺乏或功能障碍引起的,C1-INH替代疗法是HAE发作按需(急性)治疗、高风险手术前短期预防以及长期预防的一线干预措施。随机、双盲、安慰剂对照交叉试验表明,皮下注射40 - 60 IU/kg血浆源性C1-INH(pdC1-INH)、静脉注射1000 U pdC1-INH以及静脉注射50 IU/kg(最大4200 IU)重组人C1-INH(rhC1-INH)均具有剂量依赖性疗效,所有这些给药方案均为每周两次,用于有每月发作2至≥4次病史的患者进行长期预防。总体而言,高达83%(pdC1-INH 60 IU/kg)的患者发作减少阈值≥70%,高达58%(pdC1-INH 60 IU/kg)的患者发作减少阈值≥90%。较低剂量的静脉注射pdC1-INH疗法(1000 U)似乎效果较差,22名患者中有45%的发作减少阈值≥70%,高达23%的患者发作减少阈值≥90%。较高剂量的静脉注射rhC1-INH 50 IU/kg(最大,4200 IU)每周两次具有中等益处。尽管研究治疗前3个月的基线平均发作频率为17.9次,4周安慰剂期的平均发作频率为7.2次,但23名患者中有52%的发作频率降低≥70%,23名患者中有26%的发作频率降低≥90%。接受C1-INH替代疗法作为长期预防且达到这些高阈值的患者比例不断增加,增强了人们对实现“无发作”的希望和期望,包括对那些患有中度或重度疾病的患者。

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