Molecular diagnostics in the treatment of childhood acute lymphoblastic leukemia

Authors
Citation
Je. Rubnitz, Molecular diagnostics in the treatment of childhood acute lymphoblastic leukemia, J BIOL REG, 14(3), 2000, pp. 182-186
Citations number
55
Categorie Soggetti
Endocrinology, Nutrition & Metabolism
Journal title
JOURNAL OF BIOLOGICAL REGULATORS AND HOMEOSTATIC AGENTS
ISSN journal
0393974X → ACNP
Volume
14
Issue
3
Year of publication
2000
Pages
182 - 186
Database
ISI
SICI code
0393-974X(200007/09)14:3<182:MDITTO>2.0.ZU;2-2
Abstract
Somatically acquired genetic alterations play an important role in the path ogenesis of acute lymphoblastic leukemia. The molecular analysis of these a lterations has increased our understanding of the mechanisms of leukemogene sis. In addition, this information has led to improvements in our abilities to predict treatment response and to deliver the optimal intensity of trea tment to individual patients. For example, the prognosis for patients with acute lymphoblastic leukemia whose leukemic cells express the TEL-AML1 fusi on is favorable when they are treated on modem chemotherapy protocols, wher eas patients whose leukemic lymphoblasts contain the MLL-AF4 or the BCR-ABL fusion sometimes require allogeneic hematopoietic stem cell transplantatio n for cure. Molecular techniques are also used to detect minimal residual d isease and genetic polymorphisms that are important in optimizing drug ther apy.