关于血友病患者使用基因疗法的辩论

Katrina Thornber
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引用次数: 0

摘要

基因疗法是治疗甲型血友病和乙型血友病的一种创新方法,有可能提高生活质量,促进预防,甚至在某些情况下达到治疗因子水平。尽管最近的临床试验取得了初步成功,但治疗血友病的基因疗法仍是一个相对较新的研究领域,其长期安全性和有效性还有待确定。此外,目前的高昂价格也限制了大多数患者的使用。在欧洲血液学协会(EHA)2024 年大会上,一场题为 "血友病:患者接受基因疗法的机会?
本文章由计算机程序翻译,如有差异,请以英文原文为准。
A Debate on the Use of Gene Therapy in Patients with Haemophilia
GENE therapy is an innovative approach to treating haemophilia A and haemophilia B, with the potential to increase quality of life, promote prophylaxis, and even achieve curative factor levels in some cases. Despite early success in recent clinical trials, gene therapy for treating haemophilia is a relatively new area of research, and the long-term safety and efficacy are yet to be determined. Additionally, the current high price limits access for most patients. The suitability, safety, and accessibility of gene therapy for patients with haemophilia were discussed during a highly engaging debate session at the European Haematology Association (EHA) Congress 2024, titled ‘Haemophilia: Gene Therapy Access for Patients?’.
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