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我如何治疗儿童再生障碍性贫血。

How I manage aplastic anaemia in children.

机构信息

Paediatric Haematopoietic Stem Cell Transplant Unit, Department of Adolescent and Paediatric Haematology and Oncology, Great North Children's Hospital, Royal Victoria Infirmary, Newcastle Upon Tyne, UK.

出版信息

Br J Haematol. 2012 Apr;157(1):26-40. doi: 10.1111/j.1365-2141.2012.09058.x. Epub 2012 Feb 20.

Abstract

Aplastic anaemia (AA) is a rare heterogeneous condition in children. 15-20% of cases are constitutional and correct diagnosis of these inherited causes of AA is important for appropriate management. For idiopathic severe aplastic anaemia, a matched sibling donor (MSD) haematopoietic stem cell transplant (HSCT) is the treatment of choice. If a MSD is not available, the options include immunosuppressive therapy (IST) or unrelated donor HSCT. IST with horse anti-thymocyte globulin (ATG) is superior to rabbit ATG and has good long-term results. In contrast, IST with rabbit ATG has an overall response of only 30-40%. Due to improvements in outcome over the last two decades in matched unrelated donor (MUD) HSCT, results are now similar to that of MSD HSCT. The decision to proceed with IST with ATG or MUD HSCT will depend on the likelihood of finding a MUD and the differing risks and benefits that each therapy provides.

摘要

再生障碍性贫血(AA)是儿童中一种罕见的异质性疾病。15-20%的病例为先天性,正确诊断这些遗传性 AA 的病因对于适当的治疗至关重要。对于特发性严重再生障碍性贫血,匹配的同胞供体(MSD)造血干细胞移植(HSCT)是首选治疗方法。如果没有 MSD,则可以选择免疫抑制治疗(IST)或无关供体 HSCT。马抗胸腺细胞球蛋白(ATG)的 IST 优于兔 ATG,并且具有良好的长期结果。相比之下,兔 ATG 的 IST 的总体反应率仅为 30-40%。由于过去二十年中在匹配的无关供体(MUD)HSCT 方面的结果得到了改善,现在的结果与 MSD HSCT 相似。决定进行 ATG 免疫抑制治疗或 MUD HSCT 将取决于找到 MUD 的可能性,以及每种治疗方法所提供的不同风险和益处。

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