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PMID: 16115128 Published · ppublish English Journal Article

Acute myeloid leukaemia with FLT3 gene mutations of both internal tandem duplication and point mutation type.

British journal of haematology ·Vol. 130 ·No. 5 ·2005-09-00 ·Pages 726-8

Chen W, Jones D, Medeiros LJ, Luthra R, Lin P

Abstract

FLT3 gene mutations, either internal tandem duplication or point mutation type, are common in acute myeloid leukaemia (AML). We describe 21 AML cases with both types of gene mutations, so-called dual mutations, representing approximately 1% of all cases. Most newly diagnosed AML with FLT3 dual mutations had monocytic differentiation and a normal karyotype. Over the disease course, changes in FLT3 mutation status were seen in 89% of cases, and were associated with cytogenetic changes. We conclude that FLT3 dual mutations occur rarely in AML, and appear to be related to clonal evolution.

MeSH Terms
Acute Disease Adult Aged Aged, 80 and over Cloning, Molecular DNA Mutational Analysis Female Gene Duplication Humans Leukemia, Myeloid/genetics Male Middle Aged Point Mutation Proto-Oncogene Proteins/genetics Receptor Protein-Tyrosine Kinases/genetics Tandem Repeat Sequences fms-Like Tyrosine Kinase 3
Chemicals
Proto-Oncogene Proteins FLT3 protein, human Receptor Protein-Tyrosine Kinases fms-Like Tyrosine Kinase 3
Authors & Affiliations
5 authors, click to expand affiliations / ORCID
Chen Weina
Department of Hematopathology, The University of Texas M.D. Anderson Cancer Center, Houston, TX 77030, USA. weinachen@mdanderson.org
Jones Dan
Medeiros L Jeffrey
Luthra Rajyalashmi
Lin Pei
Article Info
Journal
British journal of haematology
Abbr.
Br J Haematol
ISSN
0007-1048
Published
2005-09-00
Pages
726-8
Language
English
Region
England
NLM ID
0372544
Subset
IM
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