Imai Yoichi
Department of Hematology, School of Medicine, Tokyo Women's Medical University.
Rinsho Ketsueki. 2015 Oct;56(10):1932-41. doi: 10.11406/rinketsu.56.1932.
In addition to morphological and histocytochemical analyses of acute myeloid leukemia (AML), data on cytogenetic abnormalities and somatic mutations are used for classification of AML. The risk stratification based on these examinations facilitates determining the treatment strategy for AML. Cytogenetic risk category definitions by the Southwest Oncology Group (SWOG), Cancer and Leukemia Group B (CALGB), and The Medical Research Council (MRC) classify AML patients into favorable, intermediate, and adverse groups. Approximately 80% of patients in the intermediate group have a normal karyotype and the importance of molecular genetic analyses in these patients is increasing. Somatic mutations of NPM1, CEBPA, and FLT3 are known to be related to the prognosis of AML patients. The European LeukemiaNet (ELN) introduced risk stratification for AML patients based on cytogenetic abnormalities and NPM1, CEBPA, and FLT3 mutations. This risk stratification can be used to select only chemotherapy or chemotherapy with allogeneic hematopoietic stem cell transplantation as consolidation therapy for individual AML patients. Development of molecular targeted therapies against FLT3 or IDH mutations is in progress and these novel therapies are expected to contribute to improving the prognosis of AML patients.
除了对急性髓系白血病(AML)进行形态学和组织细胞化学分析外,细胞遗传学异常和体细胞突变的数据也用于AML的分类。基于这些检查的风险分层有助于确定AML的治疗策略。西南肿瘤学组(SWOG)、癌症与白血病B组(CALGB)以及医学研究理事会(MRC)对细胞遗传学风险类别的定义将AML患者分为预后良好、中等和不良组。中等组中约80%的患者核型正常,分子遗传学分析在这些患者中的重要性日益增加。已知NPM1、CEBPA和FLT3的体细胞突变与AML患者的预后相关。欧洲白血病网(ELN)基于细胞遗传学异常以及NPM1、CEBPA和FLT3突变对AML患者进行了风险分层。这种风险分层可用于为个体AML患者选择单纯化疗或化疗联合异基因造血干细胞移植作为巩固治疗。针对FLT3或IDH突变的分子靶向治疗正在研发中,预计这些新疗法将有助于改善AML患者的预后。