CEBPA公司
净现值1
IDH1
髓系白血病
IDH2型
生存分析
内科学
背景(考古学)
医学
肿瘤科
髓样
癌症研究
白血病
生物
突变
基因
核型
遗传学
古生物学
染色体
作者
Qiuling Ma,Jinghan Wang,Yun‐Gui Wang,Chao Hu,Qitian Mu,Mengxia Yu,Lei Wang,Dongmei Wang,Min Yang,Xiufeng Yin,Feifei Chen,Shasha Lu,Jian Chen,Zhijuan Zhu,Sai‐Juan Chen,Jie Jin
摘要
The prognostic value of IDH1 mutations has been systematically evaluated in acute myeloid leukemia (AML) patients recently. However, the role of IDH1 expression in AML is still under exploration. To investigate the clinical significance, we analyzed the IDH1/2 expression in 320 patients with cytogenetically normal AML (CN‐AML) by quantitative real‐time reverse‐transcription polymerase chain reaction. High expression of IDH1 was predominant in patients with FLT3‐ ITD and DNMT3A mutations and less prevalent in cases with CEBPA double allele mutations. Strong association was observed between high IDH1 expression and low expression of microRNA 181 family. Prognosis was adversely affected by high IDH1 expression, with shorter overall survival and event‐free survival in the context of clinical characteristics, including age, WBC count, and gene mutations of NPM1 , FLT3 ‐ITD, CEBPA , IDH1 , IDH2 and DNMT3A in CN‐AML. Moreover, the clinical outcome of IDH1 expression in terms of overall survival, event‐free survival and complete remission rate still remained in multivariate models in CN‐AML. Importantly, the prognostic value was validated using the published microarray data from 79 adult patients treated according to the German AMLCG‐1999 protocol. Our results demonstrated that high IDH1 expression is associated with a poor prognosis of CN‐AML.
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