Childhood acute lymphoblastic leukemia: Integrating genomics into therapy

Cancer. 2015 Oct 15;121(20):3577-90. doi: 10.1002/cncr.29573. Epub 2015 Jul 20.

Abstract

Acute lymphoblastic leukemia (ALL), the most common malignancy of childhood, is a genetically complex entity that remains a major cause of childhood cancer-related mortality. Major advances in genomic and epigenomic profiling during the past decade have appreciably enhanced knowledge of the biology of de novo and relapsed ALL and have facilitated more precise risk stratification of patients. These achievements have also provided critical insights regarding potentially targetable lesions for the development of new therapeutic approaches in the era of precision medicine. In this review, the authors delineate the current genetic landscape of childhood ALL, emphasizing patient outcomes with contemporary treatment regimens as well as therapeutic implications of newly identified genomic alterations in specific subsets of ALL.

Keywords: acute lymphoblastic leukemia; cytogenetics; genomics; pediatrics; therapy.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't
  • Review

MeSH terms

  • Adolescent
  • Child
  • Child, Preschool
  • Genetic Predisposition to Disease
  • Genomics / methods
  • Humans
  • Infant
  • Molecular Targeted Therapy
  • Mutation*
  • Precision Medicine
  • Precursor Cell Lymphoblastic Leukemia-Lymphoma / genetics*
  • Precursor Cell Lymphoblastic Leukemia-Lymphoma / therapy*