The preferential occurrence ofFLT3-TKD mutations in inv(16) AML and impact on survival outcome: a combined analysis of 1053 core-binding factor AML patients-Reference-Cited by-同舟云学术

The preferential occurrence ofFLT3-TKD mutations in inv(16) AML and impact on survival outcome: a combined analysis of 1053 core-binding factor AML patients

Published:2012-11-28 Issue:4 Volume:160 Page:557-559
ISSN:0007-1048
Container-title:British Journal of Haematology
language:en
Short-container-title:Br J Haematol

Author:

Kok Chung H.,Brown Anna L.,Perugini Michelle,Iarossi Diana G.¹,Lewis Ian D.,D'Andrea Richard J.

Affiliation:

1. Division of Haematology and Centre for Cancer Biology; SA Pathology; Adelaide; SA; Australia

Publisher

Wiley

Subject

Hematology

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1111/bjh.12131/fullpdf

Reference8 articles.

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2. Impact of genetic features on treatment decisions in AML;Dohner;Hematology/the Education Program of the American Society of Hematology,2011

3. Meta-analysis for the potential application of FLT3-TKD mutations as prognostic indicator in non-promyelocytic AML;Li;Leukemia Research,2012

4. FLT3 tyrosine kinase domain mutations are biologically distinct from and have a significantly more favorable prognosis than FLT3 internal tandem duplications in patients with acute myeloid leukemia;Mead;Blood,2007

5. Conflicting data on the prognostic significance of FLT3/TKD mutations in acute myeloid leukemia might be related to the incidence of biallelic disease;Mead;Blood,2008

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