Suppr超能文献

伏洛妥珠单抗:一种一流的聚合抑制剂对镰状细胞病病理生理学的改变

Voxelotor: alteration of sickle cell disease pathophysiology by a first-in-class polymerization inhibitor.

作者信息

Glaros Alexander K, Razvi Reza, Shah Nirmish, Zaidi Ahmar U

机构信息

Central Michigan University, Mt. Pleasant, MI, USA.

Children's Hospital of Michigan, Detroit, MI, USA.

出版信息

Ther Adv Hematol. 2021 Mar 19;12:20406207211001136. doi: 10.1177/20406207211001136. eCollection 2021.

Abstract

Sickle cell disease, despite its recognition as a severely debilitating genetic condition affecting hundreds of thousands of neonates throughout the world each year, was not a target of pharmaceutical research focus for most of its 100-year existence in the medical consciousness. This has changed in recent years as many novel therapeutics are currently under investigation, with three new disease-modifying drugs achieving FDA approval in the last 4 years. One of these drugs, voxelotor, is especially encouraging as an inhibitor of sickling for its ability to safely improve the chronic hemolytic anemia of sickle cell disease. This was demonstrated during all clinical phases of investigation by an average improvement in hemoglobin of greater than 1 g/dL, as well as statistically significant improvements in established markers of hemolysis. While anemia itself represents a potential cause of morbidity, it is more importantly a marker of the hemolysis known to cause the long-term vascular and organ damage that makes sickle cell disease so debilitating and frequently fatal early in life. Given the recency of the approval, there has not been sufficient long-term follow-up to demonstrate improvement in the chronic sequelae of sickle cell disease as a result of voxelotor-induced improvements in hemolytic anemia. There is hope, however, based on the experience with hydroxyurea improving morbidity and mortality reductions in sickling and improved rheology, that voxelotor may have similar long-term benefits by positively manipulating the kinetics of hemoglobin polymerization. This review aims to summarize the targeted pathobiology of sickle cell disease, the mechanism of action of voxelotor, and the safety and efficacy data from preclinical to late clinical stage investigations of this long-awaited medication, in the hopes of better informing the decision-making process behind prescribing or not prescribing it for patients in need of intervention.

摘要

镰状细胞病尽管被公认为是一种严重致残的遗传病,每年影响全球数十万新生儿,但在其存在于医学认知中的100年里,大部分时间都不是药物研究的重点对象。近年来这种情况有所改变,目前有许多新型疗法正在研究中,在过去4年里有三种新型疾病修正药物获得了美国食品药品监督管理局(FDA)的批准。其中一种药物——伏索利尤单抗,作为镰变抑制剂尤其令人鼓舞,因为它能够安全地改善镰状细胞病的慢性溶血性贫血。在所有临床研究阶段都证明,血红蛋白平均改善超过1g/dL,溶血既定标志物也有统计学意义的改善。虽然贫血本身是发病的一个潜在原因,但更重要的是,它是溶血的一个标志物,已知溶血会导致长期的血管和器官损伤,使镰状细胞病如此致残,并常常在生命早期致命。鉴于批准时间较近,尚未有足够的长期随访来证明伏索利尤单抗诱导的溶血性贫血改善能使镰状细胞病的慢性后遗症得到改善。然而,基于羟基脲改善发病率和死亡率、减少镰变及改善血液流变学的经验,有希望伏索利尤单抗通过积极调控血红蛋白聚合动力学可能具有类似的长期益处。本综述旨在总结镰状细胞病的靶向病理生物学、伏索利尤单抗的作用机制,以及这种期待已久的药物从临床前到临床后期研究的安全性和有效性数据,希望能更好地为针对有干预需求的患者开具或不开具该药物的决策过程提供信息。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/34c7/7983433/984c3922c3cb/10.1177_20406207211001136-fig1.jpg

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验