Double CEBPA mutations are prognostically favorable in non-M3 acute myeloid leukemia patients with wild-type NPM1 and FLT3-ITD
| Autor: | Xiang-Mei, Wen, Jiang, Lin, Jing, Yang, Dong-Ming, Yao, Zhao-Qun, Deng, Chun-Yan, Tang, Gao-Fei, Xiao, Lei, Yang, Ji-Chun, Ma, Jia-Bo, Hu, Wei, Qian, Jun, Qian |
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| Rok vydání: | 2014 |
| Předmět: |
Adult
Male China Time Factors Adolescent DNA Mutational Analysis Kaplan-Meier Estimate Young Adult Asian People Gene Frequency Humans Genetic Predisposition to Disease Aged Proportional Hazards Models Aged 80 and over Age Factors Nuclear Proteins Middle Aged Prognosis Leukemia Myeloid Acute Phenotype fms-Like Tyrosine Kinase 3 Mutation CCAAT-Enhancer-Binding Proteins Female Original Article Nucleophosmin |
| Zdroj: | International journal of clinical and experimental pathology. 7(10) |
| ISSN: | 1936-2625 |
| Popis: | This study is aimed to investigate the pattern of CEBPA mutations and its clinical significance in Chinese non-M3 acute myeloid leukemia (AML) patients. The entire coding region of CEBPA gene was amplified by PCR and then sequenced in samples from 233 non-M3 AML patients. Fifty mutations were identified in 37 (15.8%) patients with eleven (4.7%) double mutated CEBPA (dmCEBPA) and twenty-six (11.1%) single mutated CEBPA (smCEBPA). dmCEBPA was exclusively observed in M1 and M2 subtypes of FAB classification (P = 0.008), whereas smCEBPA occurred in almost all subtypes (P = 0.401). Patients with dmCEBPA had significantly younger age and higher WBC counts than those with wtCEBPA (P = 0.016 and 0.043, respectively). Both dmCEBPA and smCEBPA were mainly present in cytogenetically normal patients. Patients with dmCEBPA achieved higher rate of complete (CR) than wtCEBPA patients (88% vs. 51%, P = 0.037), whereas smCEBPA and wtCEBPA groups are similar (47% vs. 51%, P = 0.810). Patients with dmCEBPA had a superior overall survival (OS) compared with patients with wtCEBPA (P = 0.033), whereas patients with smCEBPA had a similar OS as patients with wtCEBPA (P = 0.976). dmCEBPA but not smCEBPA was also associated with favorable outcome in patients with wild-type NPM1 and FLT3-ITD (NPM1(wt)FLT3-ITD(wt) ). Our data confirm that dmCEBPA but not smCEBPA is prognostically favorable in NPM1(wt)FLT3-ITD(wt) AML, and suggest that the entity AML with mutated CEBPA should be definitely designated as AML with dmCEBPA in WHO classification and smCEBPA should be excluded from the favorable risk of molecular abnormalities. |
| Databáze: | OpenAIRE |
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