Simoctocog alfa (Nuwiq®) in children: early steps in life's journey for people with severe hemophilia A.

IF 3.4 3区 医学 Q2 HEMATOLOGY Therapeutic Advances in Hematology Pub Date : 2024-05-09 eCollection Date: 2024-01-01 DOI:10.1177/20406207241245511
Anna Klukowska, Robert F Sidonio, Guy Young, Maria Elisa Mancuso, María Teresa Álvarez-Román, Neha Bhatnagar, Martina Jansen, Sigurd Knaub
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Abstract

People with severe hemophilia A usually experience their first bleed early in life. In children with severe hemophilia A, primary prophylaxis is recommended to prevent recurrent and potentially life-threatening bleeds that significantly impact day-to-day life. Factor VIII (FVIII) prophylaxis is well-established in children and has been shown to reduce the development of hemophilic arthropathy. However, a major challenge of FVIII therapy is the development of neutralizing anti-FVIII antibodies (FVIII inhibitors). Simoctocog alfa (Nuwiq®) is a human cell line-derived recombinant FVIII (rFVIII) whose immunogenicity, efficacy, and safety have been studied in 167 children with severe hemophilia A across two prospective clinical trials and their long-term extensions. In 105 previously untreated children, the inhibitor rate of 16.2% for high-titer inhibitors (26.7% for all inhibitors) was lower than published rates for hamster cell line-derived rFVIII products. There was no inhibitor development in previously untreated children with non-null F8 mutations and in previously treated children. In a case series of 10 inhibitor patients, 8 (80%) underwent successful immune tolerance induction with simoctocog alfa with a median time to undetectable inhibitor of 3.5 months. In an analysis of 96 children who enrolled in the extension studies and received long-term simoctocog alfa prophylaxis for up to 5 years, median spontaneous, joint, and total annualized bleeding rates were 0.3, 0.4, and 1.8, respectively. No thromboembolisms were reported in any of the 167 children, and there were no treatment-related deaths. Optimal care of children should consider several factors, including minimization of inhibitor development risk, maintaining tolerance to FVIII, highly effective bleed prevention and treatment, safety, and impact on long-term outcomes such as bone and joint health. In this context we review the pediatric clinical data and ongoing studies with simoctocog alfa.

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儿童用 Simoctocog alfa (Nuwiq®):重症 A 型血友病患者人生旅途的早期步骤。
严重 A 型血友病患者通常在生命早期就会出现第一次出血。对于患有严重 A 型血友病的儿童,建议采取一级预防措施,以防止反复发生可能危及生命的出血,因为出血会严重影响日常生活。因子 VIII(FVIII)预防疗法在儿童中已得到广泛认可,并被证明可减少血友病关节病的发生。然而,FVIII 治疗的一个主要挑战是产生中和性抗 FVIII 抗体(FVIII 抑制剂)。Simoctocog alfa(Nuwiq®)是一种人细胞系衍生的重组 FVIII(rFVIII),在两项前瞻性临床试验及其长期延长试验中,对 167 名重症 A 型血友病患儿进行了免疫原性、有效性和安全性研究。在 105 名先前未接受过治疗的儿童中,高滴度抑制剂的抑制率为 16.2%(所有抑制剂的抑制率为 26.7%),低于已公布的仓鼠细胞系衍生 rFVIII 产品的抑制率。先前未接受过治疗的非无效 F8 基因突变患儿和先前接受过治疗的患儿均未出现抑制剂。在 10 例抑制剂患者的病例系列中,有 8 例(80%)成功接受了 simoctocog alfa 的免疫耐受诱导,抑制剂检测不到的中位时间为 3.5 个月。在对 96 名参加扩展研究并接受长达 5 年的 simoctocog alfa 长期预防治疗的儿童进行的分析中,自发性出血、关节出血和总出血的中位年化出血率分别为 0.3、0.4 和 1.8。在 167 名儿童中,没有人发生血栓栓塞,也没有与治疗相关的死亡病例。儿童的最佳治疗应考虑多个因素,包括抑制剂发展风险最小化、保持对 FVIII 的耐受性、高效的出血预防和治疗、安全性以及对骨骼和关节健康等长期结果的影响。为此,我们回顾了西莫可克α的儿科临床数据和正在进行的研究。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
CiteScore
4.30
自引率
0.00%
发文量
54
审稿时长
7 weeks
期刊介绍: Therapeutic Advances in Hematology delivers the highest quality peer-reviewed articles, reviews, and scholarly comment on pioneering efforts and innovative studies across all areas of hematology. The journal has a strong clinical and pharmacological focus and is aimed at clinicians and researchers in hematology, providing a forum in print and online for publishing the highest quality articles in this area.
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