临床儿科杂志 ›› 2017, Vol. 35 ›› Issue (5): 331-.doi: 10.3969/j.issn.1000-3606.2017.05.003

• 血液肿瘤疾病专栏 • 上一篇    下一篇

EVI1 基因在儿童急性髓细胞白血病中的表达及意义

郑晨钰, 温贤浩, 郭玉霞, 管贤敏, 于洁, 肖剑文   

  1. 重庆医科大学附属儿童医院 儿童医院儿科研究所 儿童发育疾病研究教育部重点实验室 儿科学重庆市重点实验室(重庆 400014)
  • 收稿日期:2017-05-15 出版日期:2017-05-15 发布日期:2017-05-15
  • 通讯作者: 肖剑文 E-mail:tomahawk6502@sohu.com
  • 基金资助:
    重庆市卫生计生委医学科研项目(No. 2015msxm042)

Expression of EVI1 gene and its clinical significance in pediatric acute myeloid leukemia

ZHENG Chenyu, WEN Xianhao, GUO Yuxia, GUAN Xianmin, YU Jie, XIAO Jianwen   

  1. Children’s Hospital of Chongqing Medical University, Pediatric Research Institute of Children’s Hospital, Ministry of Education Key Laboratory of Child Development and Disorders, Chongqing Key Laboratory of Pediatrics, Chongqing 400014, China
  • Received:2017-05-15 Online:2017-05-15 Published:2017-05-15

摘要: 目的 探讨EVI1基因表达与儿童急性髓细胞白血病(AML)临床表现及预后的关系。方法 检测AML患儿 EVI1基因表达,分析EVI1阳性AML患儿临床和实验室检查特点以及预后。结果 145例AML患儿中EVI1阳性38例,占 26.21%。与阴性组相比,阳性组患儿的年龄、性别、血红蛋白量、白细胞及血小板计数、细胞形态学FAB分型、异常核型 检出率差异均无统计学意义(P>0.05);阴性组复杂核型检出率高于阳性组,差异有统计学意义(χ2=5.50, P=0.019)。 38例阳性患儿中,14例化疗与7例异基因造血干细胞移植(allo-HSCT)患儿的无事件生存(EFS)率差异有统计学意义 (χ2=4.00, P=0.045)。 阳性组与阴性组患儿化疗完全缓解率差异无统计学意义(91.67%对91.18%, P>0.05),阳性组患 儿复发率高于阴性组,差异有统计学意义(64.29% 对22.22%, P=0.009);两组EFS率差异也有统计学意义(χ2=5.76, P=0.015)。2例阳性组患儿骨髓复发时EVI1基因仍阴性。结论 EVI1基因是儿童AML的不良预后因素,allo-HSCT可改 善EVI1阳性AML患儿预后。定量检测EVI1基因表达可能不适用于微小残留病监测。

Abstract: Objective To investigate the relationship between EVI1 gene expression and  clinical features and prognosis of children with acute myeloid leukemia (AML). Methods EVI1 gene was detected in AML children, correlation of clinical and lab features, prognosis of AML children with EVI1 gene were analyzed. Results EVI1 expression is positive in 38 of 145 children with AML. There were no significant differences in age, gender, hemoglobin concentration, leukocytes and platelet count, subtype of morphology, ratio of chromosomal anomaly and complex karyotypes between EVI1 positive and EVI1 negative group (P>0.05); coexist genes were detected in 9 cases (23.68%) of EVI1 positive group. Rate of complete remission (CR) was 91.67% in 24 cases of EVI1 positive patients received chemotherapy. Relapse rate was 64.29% and 14.29% in EVI1 positive patients who received chemotherapy and allo-hematopoietic stem cell transplantation (allo-HSCT), retrospectively and significant differences were found (P<0.05). There was no significant difference in CR but significant difference was found in event free survival (P<0.05) for EVI1 positive and EVI1 negative patients who received chemotherapy. EVI1 gene kept negative when bone marrow relapse occurred in two patients with EVI1 positive at diagnosis. Conclusion EVI1 gene may play adverse role in pediatric AML; prognosis of EVI1 positive AML patients can be improved by allo-HSCT; follow-up of EVI1 transcript levels is insufficient to monitoring of minimal residual disease.