Comprehensive genomic profiling identifies a novel TNKS2-PDGFRA fusion that defines a myeloid neoplasm with eosinophilia that responded dramatically to imatinib therapy

Blood Cancer J. 2015 Feb 6;5(2):e278. doi: 10.1038/bcj.2014.95.
No abstract available

Publication types

  • Case Reports
  • Letter

MeSH terms

  • Benzamides / administration & dosage
  • Eosinophilia / drug therapy
  • Eosinophilia / genetics
  • Eosinophilia / pathology
  • Female
  • Genome, Human
  • High-Throughput Nucleotide Sequencing
  • Humans
  • Hypereosinophilic Syndrome / drug therapy
  • Hypereosinophilic Syndrome / genetics*
  • Hypereosinophilic Syndrome / pathology
  • Imatinib Mesylate
  • Leukemia
  • Middle Aged
  • Myeloproliferative Disorders
  • Oncogene Proteins, Fusion / genetics*
  • Oncogene Proteins, Fusion / isolation & purification
  • Piperazines / administration & dosage
  • Pyrimidines / administration & dosage
  • Receptor, Platelet-Derived Growth Factor alpha / genetics*
  • Tankyrases / genetics*

Substances

  • Benzamides
  • Oncogene Proteins, Fusion
  • Piperazines
  • Pyrimidines
  • Imatinib Mesylate
  • TNKS2 protein, human
  • Tankyrases
  • Receptor, Platelet-Derived Growth Factor alpha

Supplementary concepts

  • Pdgfra-Associated Chronic Eosinophilic Leukemia