血友病和抑制剂患者使用 Eptacog beta 的实际效果:多机构病例系列。

IF 3 2区 医学 Q2 HEMATOLOGY
Haemophilia Pub Date : 2024-09-19 DOI:10.1111/hae.15094
Kimberley Youkhana, Glaivy Batsuli, Suchitra Acharya, Osman Khan, Duc Q. Tran, Andrea Dvorak, Michael Recht, Guy Young, Robert Sidonio Jr., Yasmina Abajas
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引用次数: 0

摘要

简介:血友病 A (HA) 和血友病 B (HB) 患者在使用抑制剂治疗出血事件 (BE) 时,必须使用旁路药物。在三期临床研究中,重组 VIIa 因子旁路剂 eptacog beta 在治疗成人出血事件和控制围手术期出血方面具有疗效:这是一项回顾性病例系列研究,研究对象是在7个血友病治疗中心接受依帕可格β治疗的14名患者,他们患有HA(11例)或HB(3例),并对因子替代治疗有抑制或过敏反应:结果:共描述了 24 例自发性和外伤性 BE(肌肉血肿、关节血肿、端口部位和鼻衄),涉及 11 名受试者。在23/24例事件中,Eptacog beta作为一线疗法和治疗Eptacog alfa难治性BE的急性出血治疗均有效。当使用 Eptacog beta 进行预防治疗时,2/3 的患者报告突破性 BE 的发生频率比预防性使用 Eptacog alfa 低,1 名患者的突破性 BE 发生频率与预防性使用凝血酶原复合物浓缩物相似。有三位受试者接受了小型外科手术,乙型依帕可克能有效控制出血。据估计,使用 Eptacog beta 治疗的成本效益比 Eptacog alfa 高出 46%-72% 。没有安全问题或不良事件的报告:在这组病例中,作为一线治疗、难治性BE的治疗、围手术期出血的处理或抑制剂血友病患者的预防用药,eptacog beta是安全、有效和经济的。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Real-world effectiveness of eptacog beta in patients with haemophilia and inhibitors: A multi-institutional case series

Real-world effectiveness of eptacog beta in patients with haemophilia and inhibitors: A multi-institutional case series

Introduction

The management of bleeding events (BEs) in haemophilia A (HA) and B (HB) patients with inhibitors necessitates the use of bypassing agents. The recombinant factor VIIa bypassing agent eptacog beta has demonstrated efficacy at treating BEs and managing perioperative bleeding in adults in phase three clinical studies.

Aim

To provide real-world descriptions of eptacog beta use for BE treatment in patients on emicizumab or eptacog beta prophylaxis.

Methods

This is a retrospective case series of 14 patients who received eptacog beta at seven haemophilia treatment centres, with HA (n = 11) or HB (n = 3) and inhibitors or anaphylaxis to factor replacement.

Results

Twenty-four spontaneous and traumatic BEs are described (muscle hematomas, joint hemarthroses, port site, and epistaxis) involving 11 subjects. Eptacog beta was effective for acute bleed treatment as both first-line therapy and for treatment of BEs refractory to eptacog alfa in 23/24 events. When eptacog beta was used for prophylaxis, 2/3 patients reported a decreased frequency of breakthrough BEs compared with prophylactic eptacog alfa and one patient experienced a similar frequency of breakthrough BEs compared with prophylactic activated prothrombin complex concentrate. Eptacog beta provided effective bleed control for three subjects who underwent minor surgical procedures. Treatment with eptacog beta was estimated to be 46%–72% more cost-effective than eptacog alfa. No safety concerns or adverse events were reported.

Conclusions

In this case series, eptacog beta was safe, effective, and economical as first-line therapy, treatment of refractory BEs, management of perioperative bleeding, or prophylaxis in haemophilia patients with inhibitors.

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来源期刊
Haemophilia
Haemophilia 医学-血液学
CiteScore
6.50
自引率
28.20%
发文量
226
审稿时长
3-6 weeks
期刊介绍: Haemophilia is an international journal dedicated to the exchange of information regarding the comprehensive care of haemophilia. The Journal contains review articles, original scientific papers and case reports related to haemophilia care, with frequent supplements. Subjects covered include: clotting factor deficiencies, both inherited and acquired: haemophilia A, B, von Willebrand''s disease, deficiencies of factor V, VII, X and XI replacement therapy for clotting factor deficiencies component therapy in the developing world transfusion transmitted disease haemophilia care and paediatrics, orthopaedics, gynaecology and obstetrics nursing laboratory diagnosis carrier detection psycho-social concerns economic issues audit inherited platelet disorders.
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