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伴ETO或CBFβ阳性的急性髓细胞白血病患者c-kit基因突变的检测及意义 被引量:5

Detection of c-kit mutations in acute myeloid leukemia patients with ETO or CBFβ positive and its clinical significance
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摘要 目的:探讨伴AML1-ETO或CBFβ-MYH11阳性的急性髓细胞白血病(acute myeloid leukemia,AML)患者c-kit基因突变情况及其临床意义。方法:采用PCR结合测序的方法,对38例伴AML1-ETO或CBFβ-MYH11阳性的急性髓细胞白血病患者骨髓中c-kit外显子17的突变情况进行检测,并与患者的临床资料、实验室特征及预后的相关性进行综合分析。结果:38例患者中12例检测到c-kit外显子17突变,突变率为31.6%,其中7例为D816V突变,5例为N822K突变,两种突变类型患者的临床资料无显著差异(P>0.05),突变组骨髓原始细胞比例明显高于野生组(P<0.05),突变组与野生组患者的年龄、性别、WBC、RBC、PLT和HGB比例无明显差异(P>0.05)。c-kit突变组和野生组化疗后完全缓解率和复发率无统计学差异(P>0.05),但c-kit突变组的死亡率显著高于野生组(P<0.05)。结论:AML1-ETO或CBFβ阳性的AML患者c-kit D816V和N822K突变常见,突变患者预后差,骨髓原始细胞比例较高,c-kit基因突变检测对患者的治疗和预后有重要意义。 -ETO or CBFβ-MYH11 positive and its clinical significance. Methods:We detected the c-kit exon 17 mutations in 38 cases of AML patients with AML1-ETO or CBFβ-MYH11 positive by PCR amplification and DNA sequen-cing methods,and analyzed the correlation between c-kit mutations and its clinical characteristics,laboratorial exam-inations or prognosis. Results:C-kit mutations were found in 12 of 38 AML patients and the mutation frequency was 31.6%.Among the patients,seven had a D816V-type and five had a N822K -type mutations,which had no significant differences in patientsˊclinical characteristics(p﹥0. 05). The proportion of bone marrow blasts in mutated group was higher than those in widetype group. No significant difference was observed between the patients with and without c -kit mutations in the age,gender,the WBC,RBC and PLT counts,and HGB levels(p﹥0. 05). There was no obvious difference between c-kit mutated and widetype groups in complete remission rate and relapse rate( p﹥0. 05). However,the mortality of c-kit mutated group was higher than that of widetype group(p﹤0. 05). Conclu/sion:The D816V and N822K c-kit mutations is common in AML patients with AML1 -ETO or CBFβ-MYH11 positive who have a poor prognosis and higher bone marrow blasts proportion. The c-kit mutation detection is very important to evaluate the patientˊs prognosis and select suitable therapy.
出处 《现代肿瘤医学》 CAS 2015年第11期1581-1584,共4页 Journal of Modern Oncology
基金 国家青年科学基金项目(编号:81300420)
关键词 急性髓细胞白血病 AML1-ETO CBFβ-MYH11 C-KIT 基因突变 acute myeloid leukemia AML1 - ETO CBFβ - MYH11 c - kit gene mutation
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参考文献17

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同被引文献50

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