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急性淋巴细胞白血病

Acute lymphoblastic leukemia.

作者信息

Harrison Christine J

机构信息

Leukaemia Research Cytogenetics Group, Northern Institute for Cancer Research, Newcastle University, Level 5 Sir James Spence Institute, Royal Victoria Infirmary, Newcastle-upon-Tyne NE1 4LP, UK.

出版信息

Clin Lab Med. 2011 Dec;31(4):631-47, ix. doi: 10.1016/j.cll.2011.08.016. Epub 2011 Oct 6.

Abstract

Precursor B-ALL (BCP-ALL) is associated with a good outcome in children. Cytogenetics is one of the gold standards for risk stratification for treatment that has contributed to improved survival. Although in T-ALL genetic analysis has not been used to guide therapy, it has contributed significantly to the understanding of the biology. State-of-the-art technologies in genomic and high throughput targeted sequencing are revealing novel genetic changes linked to biological and clinical features including outcome. A number of new biomarkers provide the potential for molecular targets for therapy with promise for further improvements in survival and quality of life for ALL sufferers.

摘要

前体B淋巴细胞白血病(BCP - ALL)在儿童中预后良好。细胞遗传学是治疗风险分层的金标准之一,有助于提高生存率。虽然在T淋巴细胞白血病中,基因分析尚未用于指导治疗,但它对生物学的理解有显著贡献。基因组学和高通量靶向测序的先进技术正在揭示与生物学和临床特征(包括预后)相关的新的基因变化。一些新的生物标志物为治疗提供了分子靶点的潜力,有望进一步提高所有患者的生存率和生活质量。

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