Clinical characteristics and cytogenetic analysis of acute myeloid leukemia patients with NRAS mutation
10.3969/j.issn.1009-0754.2024.04.019
- VernacularTitle:急性髓系白血病NRAS基因突变患者临床特征及细胞遗传学分析
- Author:
Qiang LI
1
;
Xing LI
;
Pinwei ZHU
;
Zhencang ZHOU
;
Nana ZHE
;
Jinli GE
;
Dengke CHEN
Author Information
1. 563000 贵州 遵义,遵义市第一人民医院(遵义医科大学第三附属医院)
- Keywords:
Acute myeloid leukemia;
NRAS gene;
Chromosome
- From:
Journal of Navy Medicine
2024;45(4):403-407
- CountryChina
- Language:Chinese
-
Abstract:
Objective To investigate the clinical and cytogenetic characteristics of acute myeloid leukemia(AML)patients with NRAS mutations.Methods Newly diagnosed AML patients in our hospital from January 2020 to August 2022 were selected,and their clinical data were retrospectively analyzed.According to NRAS mutations,the patients were divided into NRAS mutation group and NRAS wild group.The clinical characteristics and cytogenetic differences were compared between the two groups.Results A total of 162 newly diagnosed AML patients were included in this study.There were 28 in NRAS mutation group and 134 in NRAS wild group.The peripheral white blood cell count of NRAS mutation group was significantly higher than that of NRAS wild type group(53.10×109/L vs 24.78×109/L,P<0.05).There were no significant differences in the hemoglobin level,platelet count or bone marrow blast cell count between the two groups(P>0.05).The coexisting gene mutation occurred in 25 patients(89.3%,25/28)in NRAS mutation group.The most common coexisting gene mutation was KRAS,with a mutation rate of 28.6%.Compared with NRAS wild group,NRAS mutation group was more likely to obtain KRAS mutations(P<0.05).There was no significant difference in other coexisting mutated genes between the two groups(P>0.05).The proportion of poor prognosis karyotype in the NRAS mutation group was 23.1%,which was significantly higher than that in NRAS wild group(P<0.05).The proportions of favorable and intermediate prognosis karyotypes in NRAS mutation group were 7.7%and 69.2%,respectively,which were not significantly different from those in NRAS wild group(P>0.05).Conclusion The incidence of NRAS mutation is 17.3%in AML patients in this study.Patients with NRAS mutation are more likely to have KRAS mutation and have a higher proportion of poor prognosis karyotype.
