Progress of clonal evolutionary basis of FLT3-ITD-mutant acute myeloid leukemia and the effect of its different characteristics on the prognosis
10.3760/cma.j.cn115356-20220718-00212
- VernacularTitle:急性髓系白血病FLT3-ITD突变的克隆进化基础及其不同特性对预后影响的研究进展
- Author:
Yuang GAO
1
;
Heng ZHU
;
Hongmei NING
Author Information
1. 解放军总医院第五医学中心血液病医学部,北京 100071
- Keywords:
Leukemia, myeloid, acute;
fms-like tyrosine kinase 3;
Mutation;
Drug resistance
- From:
Journal of Leukemia & Lymphoma
2023;32(9):569-572
- CountryChina
- Language:Chinese
-
Abstract:
The incidence of FLT3-internal tandem duplication (ITD) mutation in acute myeloid leukemia (AML) is approximately 20%-30% and FLT3-ITD mutation generally indicates a poor prognosis. Although FLT3 inhibitors have greatly improved the efficacy of AML patients with this type of AML, relapse and drug-resistance increasingly become prominent. ITD mutations lead to dimerization and continuous self-activation of FLT3 in the absence of ligands, and cause non-ligand-dependent phosphorylation. Different characteristics of ITD, including allele ratio, length, insertion site, wild-type mutation content and co-mutated genes, could affect the prognosis of patients. The underlying mechanism of these factors has an important guiding significance for clinical prognosis, drug application and treatment strategy.