
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.
Adult, Chromosome Aberrations, Adolescent, 610, Infant, Precursor Cell Lymphoblastic Leukemia-Lymphoma, Prognosis, Cytogenetic Analysis, Humans, Child, In Situ Hybridization, Fluorescence
Adult, Chromosome Aberrations, Adolescent, 610, Infant, Precursor Cell Lymphoblastic Leukemia-Lymphoma, Prognosis, Cytogenetic Analysis, Humans, Child, In Situ Hybridization, Fluorescence
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