Harrison Christine J
1Northern Institute for Cancer Research, Newcastle University, Newcastle-upon-Tyne, United Kingdom.
Hematology Am Soc Hematol Educ Program. 2013;2013:118-25. doi: 10.1182/asheducation-2013.1.118.
The genetics of acute lymphoblastic leukemia are becoming well understood and the incidence of individual chromosomal abnormalities varies considerably with age. Cytogenetics provide reliable risk stratification for treatment: high hyperdiploidy and ETV6-RUNX1 are good risk, whereas BCR-ABL1, MLL rearrangements, and hypodiploidy are poor risk. Nevertheless, some patients within the good- and intermediate-risk groups will unpredictably relapse. With advancing technologies in array-based approaches (single nucleotide polymorphism arrays) and next-generation sequencing to study the genome, increasing numbers of new genetic changes are being discovered. These include deletions of B-cell differentiation and cell cycle control genes, as well as mutations of genes in key signaling pathways. Their associations and interactions with established cytogenetic subgroups and with each other are becoming elucidated. Whether they have a link to outcome is the most important factor for refinement of risk factors in relation to clinical trials. For several newly identified abnormalities, including intrachromosomal amplification of chromosome 21 (iAMP21), that are associated with a poor prognosis with standard therapy, appropriately modified treatment has significantly improved outcome. After the successful use of tyrosine kinase inhibitors in the treatment of BCR-ABL1-positive acute lymphoblastic leukemia, patients with alternative ABL1 translocations and rearrangements involving PDGFRB may benefit from treatment with tyrosine kinase inhibitors. Other aberrations, for example, CRLF2 overexpression and JAK2 mutations, are also providing potential novel therapeutic targets with the prospect of reduced toxicity.
急性淋巴细胞白血病的遗传学正逐渐为人所熟知,个体染色体异常的发生率随年龄有很大差异。细胞遗传学可为治疗提供可靠的风险分层:高超二倍体和ETV6-RUNX1属于低风险,而BCR-ABL1、MLL重排和亚二倍体则属于高风险。然而,低风险和中风险组中的一些患者仍会不可预测地复发。随着基于阵列的方法(单核苷酸多态性阵列)和用于研究基因组的下一代测序技术的不断进步,越来越多新的基因变化被发现。这些变化包括B细胞分化和细胞周期控制基因的缺失,以及关键信号通路中基因的突变。它们与既定细胞遗传学亚组之间以及彼此之间的关联和相互作用正逐渐被阐明。它们是否与预后相关是完善临床试验风险因素的最重要因素。对于一些新发现的异常情况,包括21号染色体的染色体内部扩增(iAMP21),这些异常与标准治疗的不良预后相关,适当调整治疗方案已显著改善了预后。在成功使用酪氨酸激酶抑制剂治疗BCR-ABL1阳性急性淋巴细胞白血病后,具有替代ABL1易位以及涉及PDGFRB重排的患者可能会从酪氨酸激酶抑制剂治疗中获益。其他畸变,例如CRLF2过表达和JAK2突变,也提供了潜在的新型治疗靶点,有望降低毒性。