Minimal residual disease based on patient specific Flt3-ITD and -ITT mutations in acute myeloid leukemia

被引:22
|
作者
Scholl, S
Loncarevic, IF
Krause, C
Kunert, C
Clement, JH
Höffken, K
机构
[1] Univ Jena, Dept Internal Med Oncol & Hematol 2, D-07740 Jena, Germany
[2] Univ Jena, Inst Human Genet, D-6900 Jena, Germany
关键词
Flt3-ITD; AML; MRD;
D O I
10.1016/j.leukres.2004.12.001
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
We present our first experiences with determination of minimal residual disease (MRD) based on patient specific Flt3-ITD (internal tandem duplication) mutations. We analysed MRD status of 11 AML patients in a retrospective investigation and its potential impact on the follow up of these patients. In five out of six patients with a positive Flt3-ITD based MRD status a relapse of AML was observed in the follow up while one patient lacks a clinical relapse so far. In contrast, four out of five patients with a negative MRD status remain free of disease. One of these patients relapsed with a switch of FAB subtype including loss of Flt3-ITD mutation. Furthermore, in one patient we could identify a Flt3-ITT (internal tandem triplication mutation). (c) 2005 Elsevier Ltd. All rights reserved.
引用
收藏
页码:849 / 853
页数:5
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