Secker-Walker L M
Department of Haematology, Royal Free Hospital, London, England.
Cancer Genet Cytogenet. 1990 Oct 1;49(1):1-13. doi: 10.1016/0165-4608(90)90158-7.
At least 25 structural chromosomal abnormalities are now found in acute lymphoblastic leukemia (ALL). Many of the abnormalities are associated with particular clinical or blast cell features. Chromosomal translocation breakpoints in ALL are among those that define regions of the genome of oncogenic potential, the recognition of which has led to an improved understanding of the mechanisms of leukemogenesis. The prognostic importance of chromosome findings in ALL concerns demonstration of long-term survival in patients with high hyperdiploid leukemic clones and identification of patients with certain translocations who are at high risk of treatment failure and for whom alternative therapy such as bone marrow transplantation may be desirable. This review summarizes the more recent chromosomal findings in childhood and adult ALL and discusses how increasing recognition of structural change and adoption of alternative therapy for high-risk chromosomal groups may change the prognostic role of cytogenetics in this type of leukemia.
目前在急性淋巴细胞白血病(ALL)中已发现至少25种结构性染色体异常。许多异常与特定的临床或原始细胞特征相关。ALL中的染色体易位断点位于那些定义具有致癌潜力的基因组区域之中,对这些断点的识别增进了我们对白血病发生机制的理解。ALL中染色体检查结果的预后重要性在于证明高超二倍体白血病克隆患者的长期生存情况,以及识别某些易位患者,这些患者有治疗失败的高风险,可能需要骨髓移植等替代疗法。本综述总结了儿童和成人ALL中最新的染色体检查结果,并讨论了对结构变化认识的不断增加以及对高危染色体组采用替代疗法如何可能改变细胞遗传学在这类白血病中的预后作用。