Leukaemia Research Cytogenetics Group, Northern Institute for Cancer Research, Newcastle University, Newcastle-upon-Tyne, UK.
Br J Haematol. 2010 Oct;151(2):132-42. doi: 10.1111/j.1365-2141.2010.08314.x.
Treatment of childhood acute lymphoblastic leukaemia (ALL) has improved considerably in recent years. A contributing factor has been the improved stratification for treatment according to a number of factors, including genetic determinants of outcome. Here we review the current diagnostic criteria of genetic abnormalities in precursor B-ALL (BCP-ALL), including the relevant technical approaches and the application of the most appropriate methods for the detection of each abnormality. The abnormalities with the most significant impact for treatment and management of BCP-ALL are t(9;22)(q34;q11)/BCR-ABL1, t(4;11)(q21;q23)/MLL-AFF1 and near-haploidy/low hypodiploidy for high risk stratification and, to a lesser extent, t(12;21)(p13;q22)/ETV6-RUNX1 and high hyperdiploidy for good risk management. Apart from the numerical abnormalities, these can be routinely tested for by reverse transcription polymerase chain reaction, providing a basic yet informative screen. However, cytogenetics, particularly fluorescence in situ hybridization may provide reliable alternative detection methods dependent upon the preferred technical approach within each protocol.
近年来,儿童急性淋巴细胞白血病(ALL)的治疗有了显著改善。其中一个促成因素是根据多种因素(包括预后的遗传决定因素)进行治疗的分层得到了改善。在这里,我们回顾了前体 B 细胞急性淋巴细胞白血病(BCP-ALL)中遗传异常的当前诊断标准,包括相关技术方法以及每种异常的最佳检测方法的应用。对 BCP-ALL 的治疗和管理具有最重大影响的异常包括 t(9;22)(q34;q11)/BCR-ABL1、t(4;11)(q21;q23)/MLL-AFF1 和近单体性/低亚二倍体性,用于高风险分层,以及在较小程度上,t(12;21)(p13;q22)/ETV6-RUNX1 和高倍性用于良好的风险管理。除了数量异常外,这些异常通常可以通过逆转录聚合酶链反应进行常规检测,提供了基本但信息丰富的筛查。然而,细胞遗传学,特别是荧光原位杂交,可能会根据每个方案中的首选技术方法提供可靠的替代检测方法。