Laboratory for Leukemia Diagnostics, Department of Internal Medicine III, Ludwig-Maximilans-Universität, Munich, Germany; German Cancer Consortium (DKTK), Heidelberg, Germany; German Cancer Research Center (DKFZ), Heidelberg, Germany;
Laboratory for Leukemia Diagnostics, Department of Internal Medicine III, Ludwig-Maximilans-Universität, Munich, Germany;
Blood. 2016 Aug 4;128(5):686-98. doi: 10.1182/blood-2016-01-693879. Epub 2016 Jun 10.
The clinical and prognostic relevance of many recently identified driver gene mutations in adult acute myeloid leukemia (AML) is poorly defined. We sequenced the coding regions or hotspot areas of 68 recurrently mutated genes in a cohort of 664 patients aged 18 to 86 years treated on 2 phase 3 trials of the German AML Cooperative Group (AMLCG). The median number of 4 mutations per patient varied according to cytogenetic subgroup, age, and history of previous hematologic disorder or antineoplastic therapy. We found patterns of significantly comutated driver genes suggesting functional synergism. Conversely, we identified 8 virtually nonoverlapping patient subgroups, jointly comprising 78% of AML patients, that are defined by mutually exclusive genetic alterations. These subgroups, likely representing distinct underlying pathways of leukemogenesis, show widely divergent outcomes. Furthermore, we provide detailed information on associations between gene mutations, clinical patient characteristics, and therapeutic outcomes in this large cohort of uniformly treated AML patients. In multivariate analyses including a comprehensive set of molecular and clinical variables, we identified DNMT3A and RUNX1 mutations as important predictors of shorter overall survival (OS) in AML patients <60 years, and particularly in those with intermediate-risk cytogenetics. NPM1 mutations in the absence of FLT3-ITD, mutated TP53, and biallelic CEBPA mutations were identified as important molecular prognosticators of OS irrespective of patient age. In summary, our study provides a comprehensive overview of the spectrum, clinical associations, and prognostic relevance of recurrent driver gene mutations in a large cohort representing a broad spectrum and age range of intensively treated AML patients.
许多最近鉴定的成人急性髓系白血病(AML)驱动基因突变的临床和预后相关性尚未明确。我们对在德国 AML 协作组(AMLCG)的 2 项 3 期试验中治疗的 664 例 18 至 86 岁患者队列中 68 个反复突变基因的编码区或热点区域进行了测序。每个患者的 4 个突变的中位数根据细胞遗传学亚组、年龄以及先前血液系统疾病或抗肿瘤治疗的病史而有所不同。我们发现了具有显著协同作用的驱动基因突变模式。相反,我们鉴定了 8 个实际上不重叠的患者亚组,共同包含 78%的 AML 患者,这些亚组由相互排斥的遗传改变定义。这些亚组可能代表白血病发生的不同潜在途径,表现出广泛不同的结果。此外,我们还提供了有关该大型 AML 患者队列中基因突变、临床患者特征和治疗结果之间关联的详细信息。在包括综合分子和临床变量的多变量分析中,我们鉴定出 DNMT3A 和 RUNX1 突变是 60 岁以下 AML 患者总体生存率(OS)的重要预测因素,特别是对于具有中间风险细胞遗传学的患者。在没有 FLT3-ITD 的情况下 NPM1 突变、突变的 TP53 和双等位基因 CEBPA 突变被鉴定为 OS 的重要分子预后因素,而与患者年龄无关。总之,我们的研究提供了在代表广泛范围和年龄范围的大量 AML 患者中反复出现的驱动基因突变的范围、临床关联和预后相关性的综合概述。