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Blood ; 113(21): 5250-3, 2009 May 21.
Article in English | MEDLINE | ID: mdl-19279329

ABSTRACT

Mutations in the NPM1 gene represent the most frequent genetic alterations in patients with acute myeloid leukemia (AML) and are associated with a favorable outcome. In 690 normal karyotype (NK) AML patients the complete remission rates (CRs) and the percentage of patients with adequate in vivo blast cell reduction 1 week after the end of the first induction cycle were significantly higher in NPM1(+) (75% and 80%, respectively) than in NPM1(-) (57% and 57%, respectively) patients, but were unaffected by the FLT3-ITD status. Multivariate analyses revealed the presence of a NPM1 mutation as an independent positive prognostic factor for the achievement of an adequate day-16 blast clearance and a CR. In conclusion, NPM1(+) blast cells show a high in vivo sensitivity toward induction chemotherapy irrespective of the FLT3-ITD mutation status. These findings provide insight into the pathophysiology and help to understand the favorable clinical outcome of patients with NPM1(+) AML.


Subject(s)
Blast Crisis/pathology , Leukemia, Myeloid, Acute/genetics , Mutation , Myelodysplastic Syndromes/genetics , Nuclear Proteins/genetics , fms-Like Tyrosine Kinase 3/genetics , Antineoplastic Agents/pharmacology , Antineoplastic Agents/therapeutic use , Blast Crisis/drug therapy , Humans , Inverted Repeat Sequences , Karyotyping , Killer Cells, Natural , Nucleophosmin , Prognosis , Remission Induction
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