Limited clinical activity of nilotinib and sorafenib in FIP1L1-PDGFRA positive chronic eosinophilic leukemia with imatinib-resistant T674I mutation

Leukemia. 2012 Jan;26(1):162-4. doi: 10.1038/leu.2011.181. Epub 2011 Aug 5.
No abstract available

Publication types

  • Letter
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adolescent
  • Adult
  • Aged
  • Antineoplastic Agents / therapeutic use*
  • Benzamides
  • Benzenesulfonates / therapeutic use*
  • Chronic Disease
  • Drug Resistance, Neoplasm / genetics
  • Humans
  • Hypereosinophilic Syndrome / drug therapy*
  • Hypereosinophilic Syndrome / genetics
  • Imatinib Mesylate
  • Male
  • Middle Aged
  • Mutation*
  • Niacinamide / analogs & derivatives
  • Phenylurea Compounds
  • Piperazines / therapeutic use*
  • Pyridines / therapeutic use*
  • Pyrimidines / therapeutic use*
  • Receptor, Platelet-Derived Growth Factor alpha / genetics*
  • Sorafenib
  • mRNA Cleavage and Polyadenylation Factors / genetics*

Substances

  • Antineoplastic Agents
  • Benzamides
  • Benzenesulfonates
  • FIP1L1 protein, human
  • Phenylurea Compounds
  • Piperazines
  • Pyridines
  • Pyrimidines
  • mRNA Cleavage and Polyadenylation Factors
  • Niacinamide
  • Imatinib Mesylate
  • Sorafenib
  • Receptor, Platelet-Derived Growth Factor alpha
  • nilotinib