Minimal residual core binding factor AMLs by real time quantitative PCR - Initial response to chemotherapy predicts event free survival and close monitoring of peripheral blood unravels the kinetics of relapse

被引:45
作者
Stentoft, J
Hokland, P
Ostergaard, M
Hasle, H
Nyvold, CG
机构
[1] Aarhus Univ Hosp, Dept Hematol, DK-8000 Aarhus C, Denmark
[2] Aarhus Univ Hosp, Dept Pediat, Aarhus, Denmark
关键词
core binding factor leukaemia; minimal residual disease; real time quantitative PCR; leukemogenesis;
D O I
10.1016/j.leukres.2005.08.030
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Minimal residual disease (MRD) was measured by RQ-PCR in 11 AMLIIETO and 13 CBF beta/MYH11 patients at diagnosis, after induction chemotherapy, and at all subsequent visits. Median detection limits were 1:50,000 and 1:10,000, respectively. In 64/103 samples MRD was detectable and highly correlated in PB and BM. In 38/103 samples, where MRD was only detectable in BM, median BM MRD was 3.5 log lower than at diagnosis. Event free survival was significantly inferior in case of <2 log reduction post-induction MRD. Persistent MRD was always followed by hematological relapse. Molecular progression rate in relapsing CBF beta/MYH11 was surprisingly slow with a time lag to hematological relapse approaching 1 year. This direct comparison between the two subgroups of CBF AMLs delineates clear biological differences and corroborates the value of RQ-PCR. (C) 2005 Elsevier Ltd. All rights reserved.
引用
收藏
页码:389 / 395
页数:7
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