A 2-year-old with atypical CML with a t(5;12)(q33;p13) treated successfully with imatinib mesylate

Brenda Wittman; John Horan; Joanna Baxter; John Goldberg; Raymond Felgar; Erin Baylor; Bean Cromwell; Nicholas Cross; John M. Bennett

doi:10.1016/j.leukres.2003.10.011

A 2-year-old with atypical CML with a t(5;12)(q33;p13) treated successfully with imatinib mesylate

Brenda Wittman, John Horan, Joanna Baxter, John Goldberg, Raymond Felgar, Erin Baylor, Bean Cromwell, Nicholas Cross, John M. Bennett

Pediatrics

Research output: Contribution to journal › Article › peer-review

19 Scopus citations

Abstract

Atypical chronic myelogenous leukemia (aCML) is a myelodysplastic/ myeloproliferative disorder that usually occurs in older adults. Here we report a pediatric patient with aCML and a t(5;12)(q33;p13) with a corresponding fusion gene ETV6-PDGFRB. Because the PDGFRB tyrosine kinase is one of the known targets of tyrosine kinase inhibitors, this patient achieved cytogenetic and molecular remission with treatment with imatinib mesylate (formerly STI571; now Gleevec in the United States and Glivec in Europe). This case illustrates one of many myelodysplastic/myeloproliferative disorders that can be treated with this particular tyrosine kinase inhibitor.

Original language	English (US)
Pages (from-to)	65-69
Number of pages	5
Journal	Leukemia Research
Volume	28
Issue number	SUPPL. 1
DOIs	https://doi.org/10.1016/j.leukres.2003.10.011
State	Published - May 2004

Keywords

Atypical CML
ETV6-PDGFRB fusion gene
Imatinib mesylate
t(5;12)

ASJC Scopus subject areas

Cancer Research
Hematology
Oncology

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A 2-year-old with atypical CML with a t(5;12)(q33;p13) treated successfully with imatinib mesylate. / Wittman, Brenda; Horan, John; Baxter, Joanna; Goldberg, John; Felgar, Raymond; Baylor, Erin; Cromwell, Bean; Cross, Nicholas; Bennett, John M.

In: Leukemia Research, Vol. 28, No. SUPPL. 1, 05.2004, p. 65-69.

Research output: Contribution to journal › Article › peer-review

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