miR-155 expression and correlation with clinical outcome in pediatric AML: A report from Children's Oncology Group

被引:19
|
作者
Ramamurthy, Ranjani [1 ]
Hughes, Maya [2 ,3 ]
Morris, Valerie [2 ]
Bolouri, Hamid [4 ]
Gerbing, Robert B. [5 ]
Wang, Yi-Cheng [5 ]
Loken, Michael R. [6 ]
Raimondi, Susana C. [5 ,7 ]
Hirsch, Betsy A. [5 ,8 ]
Gamis, Alan S. [5 ,9 ]
Oehler, Vivian G. [1 ,2 ]
Alonzo, Todd A. [10 ]
Meshinchi, Soheil [1 ,2 ,3 ,5 ]
机构
[1] Univ Washington, Sch Med, Seattle, WA USA
[2] Fred Hutchinson Canc Res Ctr, Div Clin Res, D5-380,110 Fairview Ave North, Seattle, WA 98103 USA
[3] Seattle Childrens Hosp, Seattle, WA USA
[4] Fred Hutchinson Canc Res Ctr, Div Human Biol, 1124 Columbia St, Seattle, WA 98104 USA
[5] Childrens Oncol Grp, Monrovia, CA USA
[6] Hematol Inc, Seattle, WA USA
[7] St Jude Childrens Res Hosp, Dept Pathol, 332 N Lauderdale St, Memphis, TN 38105 USA
[8] Univ Minnesota, Div Lab Med, Med Ctr Fairview, Minneapolis, MN USA
[9] Childrens Mercy Hosp & Clin, Kansas City, MO USA
[10] Univ Southern Calif, Keck Sch Med, Dept Prevent Med, Los Angeles, CA USA
关键词
AML; children; miR-155; ACUTE MYELOID-LEUKEMIA; MICRORNA EXPRESSION; HOXA9; MUTATIONS; INFLAMMATION; TARGETS; CELLS;
D O I
10.1002/pbc.26157
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
BackgroundAberrant expression of microRNA-155 (miR-155) has been implicated in acute myeloid leukemia (AML) and associated with clinical outcome. ProcedureWe evaluated miR-155 expression in 198 children with normal karyotype AML (NK-AML) enrolled in Children's Oncology Group (COG) AML trial AAML0531 and correlated miR-155 expression levels with disease characteristics and clinical outcome. Patients were divided into quartiles (Q1-Q4) based on miR-155 expression level, and disease characteristics were then evaluated and correlated with miR-155 expression. ResultsMiR-155 expression varied over 4-log10-fold range relative to its expression in normal marrow with a median expression level of 0.825 (range 0.043-25.630) for the entire study cohort. Increasing miR-155 expression was highly associated with the presence of FLT3/ITD mutations (P < 0.001) and high-risk disease (P < 0.001) and inversely associated with standard-risk (P = 0.008) and low-risk disease (P = 0.041). Patients with highest miR-155 expression had a complete remission (CR) rate of 46% compared with 82% in low expressers (P < 0.001) with a correspondingly lower event-free (EFS) and overall survival (OS) (P < 0.001 and P = 0.002, respectively). In a multivariate model that included molecular risk factors, high miR-155 expression remained a significant independent predictor of OS (P = 0.022) and EFS (0.019). ConclusionsHigh miR-155 expression is an adverse prognostic factor in pediatric NK-AML patients. Specifically, high miR-155 expression not only correlates with FLT3/ITD mutation status and high-risk disease but it is also an independent predictor of worse EFS and OS.
引用
收藏
页码:2096 / 2103
页数:8
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