Zhao Xianfeng Frank, Gojo Ivana, York Teresa, Ning Yi, Baer Maria R
Department of Pathology, University of Maryland School of Medicine, Marlene and Stewart Greenebaum Cancer Center, Baltimore, MD 21201, USA.
Int J Clin Exp Pathol. 2009 Oct 10;3(1):75-86.
Biphenotypic acute leukemia (BAL), or acute leukemia with a single population of blasts coexpressing markers of two different lineages, is a rare clinical entity. To define BAL, a scoring system was proposed by the European Group of Immunological Markers for Leukemias (EGIL) in 1995. However, increasing evidence suggests that this system has limitations, as acknowledged by the 2008 World Health Organization (WHO) Classification of Tumors of Hematopoietic and Lymphoid Tissues. Although substantially improved in relation to the EGIL, the new WHO Classification is still not optimal for guiding the clinical management of patients with BAL. We propose a new paradigmatic approach to defining BAL based on recent clinical studies of BAL and advances in immunologic marker definition and cytogenetics, and applied our new approach to 8 cases of "BAL" among a cohort of 742 new acute leukemias in our Cancer Center. By our new criteria, 6 cases were reclassified as acute lymphoblastic leukemia (ALL), while only 2 were still classified as BAL. Our approach is also supported by analyses of the BAL cases previously reported by other institutions.
双表型急性白血病(BAL),即具有单一原始细胞群共同表达两种不同谱系标志物的急性白血病,是一种罕见的临床实体。为了定义BAL,1995年白血病免疫标志物欧洲小组(EGIL)提出了一种评分系统。然而,越来越多的证据表明该系统存在局限性,正如2008年世界卫生组织(WHO)造血与淋巴组织肿瘤分类所承认的那样。尽管相对于EGIL有了很大改进,但新的WHO分类在指导BAL患者的临床管理方面仍不理想。我们基于近期对BAL的临床研究以及免疫标志物定义和细胞遗传学方面的进展,提出了一种定义BAL的新范式方法,并将我们的新方法应用于我们癌症中心742例新发急性白血病队列中的8例“BAL”病例。根据我们的新标准,6例被重新分类为急性淋巴细胞白血病(ALL),而只有2例仍被分类为BAL。我们的方法也得到了对其他机构先前报道的BAL病例分析的支持。