FLT3-TKD by PCR

Synonyms

CD135, Fms-like tyrosine kinase 3 (FLT-3), receptor-type tyrosine-protein kinase FLT3; tyrosine kinase domain; D835; I836

  • Tech Only CPT
  • Tech Pro CPT 81246
  • PowerPath Code FLT3TKD
  • Schedule Monday - Friday (Variable)
  • Turn Around Time 2-4 days
  • Disease State Cytogenetically normal acute myeloid leukemia (CN-AML)
  • Methodology Polymerase Chain Reaction (PCR)-based fragmentation anaylsis of D835 and I836 regions of exon 20 in the FLT3 gene

Organs

Bone Marrow; Peripheral Blood

Specimen Requirements

Minimum of 1 mL whole blood in a purple (EDTA) or pink top tube (EDTA); minimum of 1 mL of bone marrow aspirate in a purple, pink, or green (heparin) top tube.

Clinical Significance

FLT3 is a receptor tyrosine kinase that is expressed on early hematopoietic progenitor cells and plays an important role in stem cell survival and differentiation. Mutations in the tyrosine kinase domain (FLT3-TKD) have been described in AML. FLT3-TKD mutations arise in the activation loop of FLT3, represented as point mutations in codon D835 or deletion of codon I836. These mutations lead to activation of the receptor tyrosine kinase.

Required Patient Info

Copy of the referring client's requisition form to accompany specimen.

Storage and Transportation

Refrigerated: 5 days; ambient (room temperature): 3 days; specimen must be received by laboratory within 7-days of collection.

Cause for Rejection

Frozen specimen; clotted or grossly hemolyzed specimens; serum; specimens without 2 patient identifiers; serum or plasma, aliquots (previously open containers); specimens that were received >7-days after collection.

Retention

2 years DNA and raw data; whole blood and bone marrow - 1 week.

Comments

This test was developed and its performance characteristics determined by CellNetix Labs LLC. The U.S. Food and Drug Administration (FDA) has not approved or cleared this test. However, FDA approval or clearance is currently not required for clinical use of this test. The results are not intended to be used as the sole means for clinical diagnosis or patient management decisions. CellNetix is authorized under Clinical Laboratory Improvement Amendments (CLIA) to perform high-complexity testing.

Vendor

LDT