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[信号转导通路基因突变对CBF-AML患者一疗程诱导缓解率的影响及临床特征分析]

[Effect of Signal Transduction Pathway Gene Mutations on the One- course Induced Remission Rate and Analysis of Clinical Characteristics in Patients with CBF-AML].

作者信息

Fan Li-Fang, Xu Jing, Chen Xiu-Hua, Tian Ting-Ting, Xie Juan, Hu Jin-Jun, Guo Zhi-Ping, Tan Yan-Hong, Xu Zhi-Fang, Ren Fang-Gang, Zhang Yao-Fang, Luo Ming, Ren Wei-Xiao, Wang Hong-Wei

机构信息

Institute of Hematology of The Second Hospital of Shanxi Medical University, Shanxi Provincial Key Laboratory of Molecular Diagnosis and Treatment of Hematological Diseases Taiyuan 030001, Shanxi Province China.

Institute of Hematology of The Second Hospital of Shanxi Medical University, Shanxi Provincial Key Laboratory of Molecular Diagnosis and Treatment of Hematological Diseases Taiyuan 030001, Shanxi Province China,E-mail:

出版信息

Zhongguo Shi Yan Xue Ye Xue Za Zhi. 2020 Jun;28(3):781-788. doi: 10.19746/j.cnki.issn.1009-2137.2020.03.011.

DOI:10.19746/j.cnki.issn.1009-2137.2020.03.011
PMID:32552936
Abstract

OBJECTIVE

To investigate the effect of other gene mutations outside the fusion gene on the first complete remission (CR) induced by one course of induction chemotherapy in patients with core binding factor-associated acute myeloid leukemia (CBF-AML).

METHODS

DNA was extracted from bone marrow or peripheral blood samples of newly diagnosed CBF-AML patients admitted to the Hematology Department of the Second Hospital of Shanxi Medical University from January 2015 to January 2019. Next-generation sequencing was used for detection of 34 kinds of hematologic malignancy-related gene mutations in patients with CBF-AML, the effect of related gene mutations on the first complete remission (CR) rate in one course of induction chemotherapy was analyzed by combineation with clinical characteristics.

RESULTS

34 kinds of genes in bone marrow or peripheral blood of 43 patients were detected by high throughput sequencing and the gene mutations were detected in 16 out of 34 genes. The mutation rate of KIT gene was the highest (48.8%), followed by NRAS (16.3%), ASXL1 (16.3%), TET2 (11.6%), CSF3R (9.3%), FLT3 (9.3%), KRAS (7.0%). The detection rates of mutations in different functional genes were as follows: genes related with signal transduction pathway (KIT, FLT3, CSF3R, KRAS, NRAS, JAK2, CALR, SH2B3, CBL) had the highest mutation frequency (72.1% (31/43); epigenetic modification gene mutation frequency was 30.2% (13/43), including ASXL1, TET2, BCOR); transcriptional regulation gene mutation frequency was 7.0% (3/43), including ETV6, RUNX1, GATA2). Splicing factor related gene mutation frequency was 2.3% (1/43), including ZRSR2). The CR rate was 74.4% after one course of induction chemotherapy. At first diagnosis, patients with low expression of WT1 (the median value of WT1 was 788.9) were more likely to get CR (P=0.032) and the RFS of patients who got CR after one course of induction chemotherapy was significantly longer than that of patients without CR [7.6 (2.2-44.1) versus 5.8 (1-19.4), (P=0.048)]. The rate of CR in the signal transduction pathway gene mutation group was significantly lower than that in non-mutation group (64.5% vs 100%) (P=0.045), while the level of serum hydroxybutyrate dehydrogenase (HBDH) was significantly higher than that in non-mutation group [(418 (154-2702) vs 246 (110-1068)] (P=0.032). There was no difference in CD56 expression between the two groups (P=0.053), which was limited to the difference between (≥20%) expression and non-expression. (P=0.048).

CONCLUSION

CBF-AML patients with signal transduction pathway gene mutation are often accompanied by high HBDH level and CD56 expression, moreover, the remission rate induced by one course of treatment is low.

摘要

目的

探讨核心结合因子相关急性髓系白血病(CBF-AML)患者融合基因以外的其他基因突变对一个疗程诱导化疗所致首次完全缓解(CR)的影响。

方法

提取2015年1月至2019年1月在山西医科大学第二医院血液科住院的初诊CBF-AML患者骨髓或外周血样本的DNA。采用二代测序技术检测CBF-AML患者34种血液系统恶性肿瘤相关基因突变情况,并结合临床特征分析相关基因突变对一个疗程诱导化疗首次完全缓解(CR)率的影响。

结果

对43例患者骨髓或外周血中的34种基因进行高通量测序,共检测到34种基因中的16种发生基因突变。KIT基因的突变率最高(48.8%),其次为NRAS(16.3%)、ASXL1(16.3%)、TET2(11.6%)、CSF3R(9.3%)、FLT3(9.3%)、KRAS(7.0%)。不同功能基因的突变检出率如下:与信号转导通路相关基因(KIT、FLT3、CSF3R、KRAS、NRAS、JAK2、CALR、SH2B3、CBL)的突变频率最高(72.1%(31/43));表观遗传修饰基因突变频率为30.2%(13/43),包括ASXL1、TET2、BCOR;转录调控基因突变频率为7.0%(3/43),包括ETV6、RUNX1、GATA2;剪接因子相关基因突变频率为2.3%(1/43),包括ZRSR2。一个疗程诱导化疗后的CR率为74.4%。初诊时WT1低表达(WT1中位数为788.9)的患者更易获得CR(P=0.032),一个疗程诱导化疗后获得CR的患者的无复发生存期显著长于未获得CR的患者[7.6(2.2 - 44.1)对5.8(1 - 19.4),(P=0.048)]。信号转导通路基因突变组的CR率显著低于非突变组(64.5%对100%)(P=0.045),而血清羟丁酸脱氢酶(HBDH)水平显著高于非突变组[(418(154 - 2702)对246(110 - 1068)](P=0.032)。两组间CD56表达无差异(P=0.053),仅限于(≥20%)表达与未表达之间的差异(P=0.048)。

结论

信号转导通路基因突变的CBF-AML患者常伴有较高的HBDH水平和CD56表达,且一个疗程治疗诱导的缓解率较低。

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