Prognosis and monitoring of core-binding factor acute myeloid leukemia: current and emerging factors

被引:23
作者
Duployez, Nicolas [1 ,2 ]
Willekens, Christophe [3 ]
Marceau-Renaut, Alice [1 ,2 ]
Boudry-Labis, Elise [2 ,4 ]
Preudhomme, Claude [1 ,2 ]
机构
[1] Lille Univ Hosp, Hematol Lab, Biol & Pathol Ctr, Lille, France
[2] INSERM, Team 3, U837, F-59045 Lille, France
[3] Dept Hematol, Villejuif, France
[4] Lille Univ Hosp, Med Genet Lab, Lille, France
基金
英国医学研究理事会;
关键词
acute myeloid leukemia; CBFB-MYH11; core binding factor; minimal residual disease; mutational analysis; prognostic markers; RUNX1-RUNX1T1; MINIMAL RESIDUAL DISEASE; ACUTE MYELOGENOUS LEUKEMIA; TIME QUANTITATIVE PCR; BLOOD-CELL COUNT; BALANCED CHROMOSOME-ABERRATIONS; JAK2-V617F ACTIVATING MUTATION; INTERNAL TANDEM DUPLICATION; POLYMERASE-CHAIN-REACTION; DATA-BASED METAANALYSIS; C-KIT;
D O I
10.1586/17474086.2014.976551
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Core-binding factor acute myeloid leukemia (CBF-AML) - including AML with t(8;21) and AML with inv(16) - accounts for about 15% of adult AML and is associated with a relatively favorable prognosis. Nonetheless, relapse incidence may reach 40% in these patients. In this context, identification of prognostic markers is considered of great interest. Due to similarities between their molecular and prognostic features, t(8;21) and inv(16)-AML are usually grouped and reported together in clinical studies. However, considerable experimental evidences have highlighted that they represent two distinct entities and should be considered separately for further studies. This review summarizes recent laboratory and clinical findings in this particular subset of AML and how they could be used to improve management of patients in routine practice.
引用
收藏
页码:43 / 56
页数:14
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