Institute of Hematology, University of Perugia, Ospedale S. Maria della Misericordia, S. Andrea delle Fratte, Perugia, Italy.
Blood. 2011 Jan 27;117(4):1109-20. doi: 10.1182/blood-2010-08-299990. Epub 2010 Oct 28.
After the discovery of NPM1-mutated acute myeloid leukemia (AML) in 2005 and its subsequent inclusion as a provisional entity in the 2008 World Health Organization classification of myeloid neoplasms, several controversial issues remained to be clarified. It was unclear whether the NPM1 mutation was a primary genetic lesion and whether additional chromosomal aberrations and multilineage dysplasia had any impact on the biologic and prognostic features of NPM1-mutated AML. Moreover, it was uncertain how to classify AML patients who were double-mutated for NPM1 and CEBPA. Recent studies have shown that: (1) the NPM1 mutant perturbs hemopoiesis in experimental models; (2) leukemic stem cells from NPM1-mutated AML patients carry the mutation; and (3) the NPM1 mutation is usually mutually exclusive of biallelic CEPBA mutations. Moreover, the biologic and clinical features of NPM1-mutated AML do not seem to be significantly influenced by concomitant chromosomal aberrations or multilineage dysplasia. Altogether, these pieces of evidence point to NPM1-mutated AML as a founder genetic event that defines a distinct leukemia entity accounting for approximately one-third of all AML.
2005 年发现 NPM1 突变型急性髓系白血病(AML)后,其于 2008 年被世界卫生组织(WHO)髓系肿瘤分类纳入临时实体,此后仍有一些有争议的问题需要阐明。当时还不清楚 NPM1 突变是否是原发性遗传病变,以及是否存在其他染色体异常和多系发育不良会对 NPM1 突变型 AML 的生物学和预后特征产生影响。此外,对于同时存在 NPM1 和 CEBPA 双突变的 AML 患者如何分类也不确定。最近的研究表明:(1)NPM1 突变体在实验模型中扰乱造血;(2)NPM1 突变型 AML 患者的白血病干细胞携带该突变;(3)NPM1 突变通常与双等位基因 CEPBA 突变相互排斥。此外,NPM1 突变型 AML 的生物学和临床特征似乎不受伴随的染色体异常或多系发育不良的显著影响。总之,这些证据表明 NPM1 突变型 AML 是一种创始性遗传事件,定义了一种独特的白血病实体,约占所有 AML 的三分之一。