Activating FLT3 mutations in CD117/KIT+ T-cell acute lymphoblastic leukemias Academic Article uri icon

Overview

MeSH Major

  • Precursor Cell Lymphoblastic Leukemia-Lymphoma
  • Proto-Oncogene Proteins
  • Proto-Oncogene Proteins c-kit
  • Receptor Protein-Tyrosine Kinases

abstract

  • Activating FLT3 mutations are the most common genetic aberrations in acute myeloid leukemia (AML), resulting in the constitutive activation of this receptor tyrosine kinase (RTK), but such mutations are rarely found in acute lymphoblastic leukemia (ALL). Here we describe a unique subset of de novo adult T-cell ALL (T-ALL) cases that coexpress CD117/KIT and cytoplasmic CD3 (CD117/KIT(+) ALL). Activating mutations in the FLT3 RTK gene were found in each of 3 CD117/KIT(+) cases that were analyzed, but not in 52 other adult T-ALL samples from the same series that lacked CD117/KIT expression. Our results indicate the need for clinical trials to test the efficacy of drugs that inhibit the FLT3 RTK in this subset of patients with T-ALL.

publication date

  • July 15, 2004

Research

keywords

  • Academic Article

Identity

Language

  • eng

Digital Object Identifier (DOI)

  • 10.1182/blood-2004-01-0168

PubMed ID

  • 15044257

Additional Document Info

start page

  • 558

end page

  • 60

volume

  • 104

number

  • 2