Core binding factor acute myeloid leukemia (CBF-AML): is high-dose Ara-C (HDAC) consolidation as effective as you think?

被引:27
作者
Dombret, Herve [1 ]
Preudhomme, Claude [2 ]
Boissel, Nicolas
机构
[1] Univ Paris 07, Hop St Louis, Inst Univ Hematol, AP HP,Dept Hematol, 1 Ave Claude Vellefaux, F-75010 Paris, France
[2] CHRU Lille, Hop Claude Hurriez, Hematol Lab, Lille, France
关键词
acute myeloid leukemia; core binding factor; gene expression profiling; KIT mutations; minimal residual disease; STEM-CELL TRANSPLANTATION; MINIMAL RESIDUAL DISEASE; 1ST COMPLETE REMISSION; ACUTE MYELOGENOUS LEUKEMIA; TIMED-SEQUENTIAL INDUCTION; POLYMERASE-CHAIN-REACTION; LONG-TERM ANALYSIS; KIT MUTATIONS; PROGNOSTIC IMPACT; RANDOMIZED-TRIAL;
D O I
10.1097/MOH.0b013e3283257b18
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Purpose of review Core binding factor acute myeloid leukemia (CBF-AML) corresponds to two distinct subtypes of AML characterized by recurrent favorable chromosome translocations, namely t(8;21) and inv(16)/t(16;16). Given the relatively good outcome of patients with CBF-AML, when treated with intensive chemotherapy including high-dose cytarabine, they are generally not considered as candidates for intensification with allogeneic stem cell transplantation in the first complete remission. The optimal treatment strategy (place of stem cell transplantation, best postremission chemotherapy, role of targeted agents) remains, however, to be defined in these patients. Recent findings The biological and prognostic heterogeneity of both CBF-AML subtypes, including gene mutation and gene expression profiles as well as molecular response to therapy, has been recently described. Summary These new insights in the heterogeneity of CBF-AML suggest that a tailored approach might be preferred to a unique predefined strategy to treat these patients.
引用
收藏
页码:92 / 97
页数:6
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