Jiménez-Yuste Victor
Department of Haematology, Hospital Universitario La Paz-IdiPaz, Autónoma University, Madrid, Spain.
Semin Thromb Hemost. 2025 Feb;51(1):23-27. doi: 10.1055/s-0044-1796651. Epub 2024 Nov 29.
Non-factor replacement therapies (NFTs) have been developed to address the limitations of conventional replacement therapies, aiming to improve hemostasis and provide enhanced protection against bleeding episodes and long-term joint damage for patients both with and without inhibitors. Factor VIII (FVIII)-mimetic agents, such as emicizumab, have transformed the management of hemophilia A with inhibitors, offering a lower treatment burden and an effective alternative for those without inhibitors as well. Rebalancing agents, including anti-tissular factor pathway inhibitor agents (concizumab and marstacimab) and serpin inhibitors like fitusiran, have shown promising efficacy for patients with hemophilia B with inhibitors and other hemophilia subtypes. Administered subcutaneously, NFTs generate stable thrombin levels and feature a long half-life, which can shift severe hemophilia toward a milder phenotype. These therapies are effective regardless of inhibitor status and hold potential for application in other bleeding disorders. Evaluating the potential thrombotic risk after implementing mitigation measures, along with the development of anti-drug antibodies (ADAs), remain critical areas for further analysis. NFTs pose additional challenges due to their complex mechanism of action and the absence of a standardized laboratory assessment method. Unresolved issues include optimal management strategies for major surgeries and tailored approaches for safe use in older populations. This review highlights the progress and future potential of NFTs in treating persons with hemophilia.
非因子替代疗法(NFTs)已被开发出来以解决传统替代疗法的局限性,旨在改善止血功能,并为有和没有抑制剂的患者提供增强的保护,防止出血发作和长期关节损伤。因子VIII(FVIII)模拟剂,如艾美赛珠单抗,已经改变了伴有抑制剂的A型血友病的治疗方式,对于没有抑制剂的患者来说,也提供了更低的治疗负担和有效的替代方案。再平衡剂,包括抗组织因子途径抑制剂(康西珠单抗和玛斯塔西单抗)以及丝氨酸蛋白酶抑制剂(如fitusiran),已显示出对伴有抑制剂的B型血友病患者和其他血友病亚型有良好疗效。通过皮下给药,NFTs可产生稳定的凝血酶水平,且半衰期长,这可使重度血友病转变为较轻的表型。这些疗法无论抑制剂状态如何均有效,并且在其他出血性疾病中具有应用潜力。在实施缓解措施后评估潜在的血栓形成风险以及抗药物抗体(ADA)的产生,仍然是需要进一步分析的关键领域。由于其复杂的作用机制和缺乏标准化的实验室评估方法,NFTs带来了额外的挑战。未解决的问题包括重大手术的最佳管理策略以及针对老年人群安全使用的定制方法。本综述强调了NFTs在治疗血友病患者方面的进展和未来潜力。