Long-term follow-up of ETV6-RUNX1 ALL reveals that NCI risk, rather than secondary genetic abnormalities, is the key risk factor

被引:22
作者
Enshaei, A. [1 ]
Schwab, C. J. [1 ]
Konn, Z. J. [1 ]
Mitchell, C. D. [2 ]
Kinsey, S. E. [3 ,4 ]
Wade, R. [5 ]
Vora, A. [6 ]
Harrison, C. J. [1 ]
Moorman, A. V. [1 ]
机构
[1] Newcastle Univ, Northern Inst Canc Res, Leukaemia Res Cytogenet Grp, Newcastle Upon Tyne NE1 7RU, Tyne & Wear, England
[2] John Radcliffe Hosp, Dept Paediat Oncol, Oxford OX3 9DU, England
[3] Leeds Gen Infirm, Dept Paediat Haematol & Oncol, Leeds, W Yorkshire, England
[4] Univ Leeds, Leeds Inst Mol Med, Leeds, W Yorkshire, England
[5] Univ Oxford, Clin Trial Serv Unit, Oxford, England
[6] Sheffield Childrens Hosp, Dept Haematol, Sheffield, S Yorkshire, England
基金
英国医学研究理事会;
关键词
ACUTE LYMPHOBLASTIC-LEUKEMIA; REARRANGEMENTS; PROTOCOL; IMPACT; ETV6; TEL;
D O I
10.1038/leu.2013.136
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
引用
收藏
页码:2256 / 2259
页数:5
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