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双特异性抗体emicizumab 治疗 A 型血友病:抑制剂患者的突破。

Bispecific Antibody Emicizumab for Haemophilia A: A Breakthrough for Patients with Inhibitors.

机构信息

Hemophilia Comprehensive Care Centre, Charlotte Maxeke Johannesburg Academic Hospital and Faculty of Health Sciences, University of the Witwatersrand and NHLS, 7 York Road, Parktown, Johannesburg, 2193, South Africa.

出版信息

BioDrugs. 2018 Dec;32(6):561-570. doi: 10.1007/s40259-018-0315-0.

Abstract

Current unmet needs in haemophilia A patients with inhibitors include the need for intravenous infusion of replacement therapy and the high burden of treatment associated with prophylaxis. Emicizumab is a humanised bispecific monoclonal antibody designed to address these unmet needs and has completed phase III clinical trials in adolescents/adults (HAVEN 1) and paediatric (HAVEN 2) inhibitor populations. In HAVEN 1, there was an 80% bleed reduction across all bleeds, 89% reduction in treated joint bleeds, 92% reduction in treated spontaneous bleeds, and 95% reduction in treated target joint bleeds on emicizumab compared with no prophylaxis. In HAVEN 2, there was a 63% reduction in all bleeds, 94.7% reduction in treated bleeds, 94.7% reduction in treated spontaneous bleeds, 100% reduction in treated joint bleeds, and 100% reduction in treated target joint bleeds on emicizumab prophylaxis when compared with no prophylaxis. For patients on bypassing agent prophylaxis, emicizumab resulted in a 68% reduction in bleeds in HAVEN 1 and a 100% reduction in bleed rates in HAVEN 2. In HAVEN 1, three patients developed thrombotic microangiopathy (TMA) and two developed thrombosis when emicizumab was used together with an activated prothrombin complex concentrate (aPCC) at high or frequent doses. When the combination was avoided in HAVEN 2, no patient developed TMA or thrombosis. In both studies, no anti-emicizumab antibodies developed and the pharmacokinetic profile of emicizumab was similar. Emicizumab use is currently being explored in haemophilia A patients without inhibitors as well as in combination with other haemophilia A replacement therapies. The role of emicizumab in combination with current factor VIII replacement therapies and evolving non-replacement therapies remains to be established.

摘要

目前,患有抑制剂的血友病 A 患者存在未满足的需求,包括需要静脉输注替代疗法以及预防治疗相关的高负担。依库珠单抗是一种人源化双特异性单克隆抗体,旨在满足这些未满足的需求,并已完成青少年/成年(HAVEN 1)和儿科(HAVEN 2)抑制剂人群的 III 期临床试验。在 HAVEN 1 中,与未预防相比,所有出血减少 80%,治疗关节出血减少 89%,治疗自发性出血减少 92%,治疗目标关节出血减少 95%。在 HAVEN 2 中,与未预防相比,所有出血减少 63%,治疗出血减少 94.7%,治疗自发性出血减少 94.7%,治疗关节出血减少 100%,治疗目标关节出血减少 100%。对于接受旁路剂预防的患者,依库珠单抗预防可使 HAVEN 1 中的出血减少 68%,HAVEN 2 中的出血率降低 100%。在 HAVEN 1 中,有 3 名患者在使用依库珠单抗联合高剂量或频繁剂量的活化凝血酶原复合物浓缩物(aPCC)时发生血栓性微血管病(TMA),2 名患者发生血栓形成。当在 HAVEN 2 中避免使用该联合治疗时,没有患者发生 TMA 或血栓形成。在这两项研究中,均未发现抗依库珠单抗抗体,依库珠单抗的药代动力学特征相似。目前正在探索依库珠单抗在无抑制剂的血友病 A 患者以及与其他血友病 A 替代疗法联合使用中的作用。依库珠单抗与目前的因子 VIII 替代疗法和不断发展的非替代疗法联合应用的作用仍有待确定。

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