我如何治疗FLT3突变的急性髓系白血病。

How I treat FLT3-mutated AML.

作者信息

Pratz Keith W, Levis Mark

机构信息

Sidney Kimmel Comprehensive Cancer Center, Johns Hopkins University, Baltimore, MD.

出版信息

Blood. 2017 Feb 2;129(5):565-571. doi: 10.1182/blood-2016-09-693648. Epub 2016 Nov 21.

Abstract

FLT3-mutated acute myeloid leukemia (AML), despite not being recognized as a distinct entity in the World Health Organization (WHO) classification system, is readily recognized as a particular challenge by clinical specialists who treat acute leukemia. This is especially true with regards to the patients harboring the most common type of FLT3 mutation, the internal tandem duplication (FLT3-ITD) mutation. Here we present 4 patient cases from our institution and discuss how our management reflects what we have learned about this subtype of the disease. We also reflect on how we anticipate the management might change in the near future, with the emergence of clinically useful tyrosine kinase inhibitors.

摘要

FLT3突变的急性髓系白血病(AML),尽管在世界卫生组织(WHO)分类系统中未被视为一个独特的实体,但治疗急性白血病的临床专家很容易将其视为一项特殊挑战。对于携带最常见FLT3突变类型即内部串联重复(FLT3-ITD)突变的患者而言尤其如此。在此,我们展示了来自我们机构的4例患者病例,并讨论我们的治疗方法如何反映我们对该疾病亚型的认识。我们还思考随着临床上有用的酪氨酸激酶抑制剂的出现,我们预计在不久的将来治疗方法可能会如何改变。

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