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1.
Br J Haematol ; 204(3): 939-944, 2024 Mar.
Artículo en Inglés | MEDLINE | ID: mdl-38054248

RESUMEN

Trisomy karyotype occurs in 5%-10% of AML. Its mutational landscape and prognostic significance are not well defined. A cohort of 156 trisomy AML patients was analysed, with reference to 615 cytogenetically normal (CN) AML patients. Trisomy AML showed distinct mutational landscape with more prevalent SMC1A, N/KRAS, ASXL1 and BCOR but fewer CEBPAbZIP and NPM1 mutations in patients ≤60, and fewer NPM1 mutations in those >60. NRAS mutations were associated with poor outcome in trisomy AML, whereas DNMT3A and FLT3-ITD mutations had neutral effect. Trisomy AML appeared biologically distinct from CN-AML.


Asunto(s)
Leucemia Mieloide Aguda , Proteínas Nucleares , Humanos , Proteínas Nucleares/genética , Nucleofosmina , Leucemia Mieloide Aguda/genética , Trisomía , Mutación , Cariotipo , Pronóstico , Tirosina Quinasa 3 Similar a fms/genética
3.
Ann Hematol ; 99(12): 2949-2952, 2020 Dec.
Artículo en Inglés | MEDLINE | ID: mdl-32514627
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