Evidence map›Paper›PMID 21747880›Full record

ArticleThe Korean journal of hematology2011

Prognostic significance of the FLT3 ITD mutation in patients with normal-karyotype acute myeloid leukemia in relapse.

Sang Hyuk Park, Hyun-Sook Chi, Sook-Kyung Min, Young-Uk Cho, Seongsoo Jang, Chan-Jeoung Park, Jung-Hee Lee, Je-Hwan Lee, Kyoo-Hyung Lee, Ho-Joon Im and 1 more

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Article in The Korean journal of hematology, 2011. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

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2citing papers in PubMed
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1 · What the graph read from it

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3 · Its place in the literature

Who cites it

2 citing papers in PubMed.

  1. Absence of FLT3 mutations in Iranian adult T-cell leukemia/lymphoma patients.Medical journal of the Islamic Republic of Iran · 2018
    Article
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4 · The record

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5 · Who and what money

Authors and funding

11 authors.

Sang Hyuk ParkDepartment of Laboratory Medicine, University of Ulsan College of Medicine and Asan Medical Center, Seoul, Korea.
Hyun-Sook Chi
Sook-Kyung Min
Young-Uk Cho
Seongsoo Jang
Chan-Jeoung Park
Jung-Hee Lee
Je-Hwan Lee
Kyoo-Hyung Lee
Ho-Joon Im
Jong-Jin Seo

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundFms-like tyrosine kinase 3 internal tandem duplication (FLT3 ITD) mutation is related to poor prognosis in normal-karyotype acute myeloid leukemia (AML). However, the prognostic significance of the mutation at relapse has not been adequately investigated. We investigated the prognostic significance of the FLT3 ITD mutation at relapse in normal-karyotype AML patients.

methodsWe analyzed 69 normal-karyotype AML patients, in whom paired bone marrow samples taken at initial diagnosis and subsequent relapse were analyzed for the FLT3 ITD mutation at the Asan Medical Center between 1995 and 2009.

resultsForty patients showed a persistent wild-type genotype, 11 showed the FLT3 ITD mutation at diagnosis and relapse, and 9 lost and another 9 acquired the mutation at relapse. The mutation status at relapse affected the overall survival (OS), with the mutation group showing shorter OS and survival after relapse than the wild-type group did (P<0.001 and P<0.001, respectively), despite having received more frequent stem cell transplantation after relapse than the wild-type group did. However, no difference was detected in the OS and survival after relapse with regard to the mutation status at diagnosis.

conclusionThe patients with FLT3 ITD mutation at relapse showed poorer prognoses than those without the mutation. However, mutation status at diagnosis did not affect the outcome. These results suggest that, in normal-karyotype AML patients with relapse, the prognostic significance of FLT3 ITD mutation at relapse is greater than that of the mutation status at diagnosis.

Indexed as

AMLFLT3 ITDNormal karyotypePrognosisRelapse

Identifiers

PMID21747880
PMCPMC3128906

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