去纤维肽——治疗严重静脉闭塞疾病的新方法

Q4 Medicine
Katrina Mountfort, M. Mohty, E. Wallhult
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引用次数: 0

摘要

严重静脉闭塞性疾病(VOD)是造血干细胞移植(HSCT)的一种严重且危及生命的并发症,其治疗标准直到最近都是支持性治疗。VOD是鼻窦内皮细胞原发性损伤的结果,严重的VOD以鼻窦狭窄和闭塞为特征,导致门静脉高压、多器官功能衰竭(MOF),最终导致死亡。Defibrotide调节VOD病理过程中涉及的多种途径,是欧洲首个批准用于治疗重度VOD的药物。去纤肽适用于成人和1个月以上婴儿的HSCT治疗中严重肝脏VOD的治疗。一项III期研究发现,与历史对照组相比,去纤维肽治疗的完全缓解(CR)和生存期显著增加。这些数据以及早期研究和正在进行的大型患者队列扩展访问协议表明,使用去纤维肽可改善严重VOD的预后,并强调了使用去纤维肽治疗的重要性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Defibrotide – A New Treatment Approach for Severe Veno-occlusive Disease
Touch MEDical MEDia 11 Abstract Severe veno-occlusive disease (VOD) is a serious and life-threatening complication of haematopoietic stem cell transplantation (HSCT), for which the standard of care has until recently been supportive care. VOD is the result of a primary injury to sinusoidal endothelial cells and severe VOD is characterised by sinusoidal narrowing and occlusion, which leads to portal hypertension, multi-organ failure (MOF) and, ultimately, death. Defibrotide regulates multiple pathways involved in the pathological processes underlying VOD and is the first drug to be approved in Europe for the treatment of severe VOD. Defibrotide is indicated for the treatment of severe hepatic VOD in HSCT therapy in adults and infants aged over 1 month. A phase III study found significant increases in complete response (CR) and survival with defibrotide compared with historical controls. These data together with earlier studies and an ongoing expanded access protocol in a large patient cohort demonstrate improved outcomes with defibrotide in severe VOD and highlight the importance of treatment with defibrotide.
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来源期刊
European Oncology and Haematology
European Oncology and Haematology Medicine-Hematology
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