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Br J Haematol ; 166(2): 254-259, 2014 Jul.
Article in English | MEDLINE | ID: mdl-24661089

ABSTRACT

Acute myeloid leukaemia (AML) with t(6;9)(p23;q34) is a rare subtype associated with FLT3-internal tandem duplication (ITD) and poor outcomes. The clinical outcomes of paediatric patients with t(6;9) with and without FLT3-ITD treated on six consecutive cooperative trails were evaluated. In contrast to patients without t(6;9), those with t(6;9) had a significantly lower complete remission rate, higher relapse rate (RR), and poor overall survival (OS). Within t(6;9) patients, those with and without FLT3-ITD had an OS of 40% and 27% respectively (P > 0·9), demonstrating that t(6;9) is a high-risk cytogenetic feature in paediatric AML and its clinical impact is independent of the presence of FLT3-ITD.


Subject(s)
Chromosomes, Human, Pair 6/genetics , Chromosomes, Human, Pair 9/genetics , Leukemia, Myeloid, Acute/genetics , Translocation, Genetic , fms-Like Tyrosine Kinase 3/genetics , Adolescent , Adult , Child , Child, Preschool , Female , Gene Duplication , Genes, Neoplasm , Humans , Infant , Infant, Newborn , Leukemia, Myeloid, Acute/therapy , Male , Neoplasm Proteins/genetics , Prognosis , Recurrence , Remission Induction , Survival Analysis , Tandem Repeat Sequences , Treatment Outcome
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