Favorable outcome of patients with acute myeloid leukemia harboring a low-allelic burden FLT3-ITD mutation and concomitant NPM1 mutation: relevance to post-remission therapy.

نویسندگان

  • Marta Pratcorona
  • Salut Brunet
  • Josep Nomdedéu
  • Josep Maria Ribera
  • Mar Tormo
  • Rafael Duarte
  • Lourdes Escoda
  • Ramon Guàrdia
  • M Paz Queipo de Llano
  • Olga Salamero
  • Joan Bargay
  • Carmen Pedro
  • Josep Maria Martí
  • Montserrat Torrebadell
  • Marina Díaz-Beyá
  • Mireia Camós
  • Dolors Colomer
  • Montserrat Hoyos
  • Jorge Sierra
  • Jordi Esteve
چکیده

Risk associated to FLT3 internal tandem duplication (FLT3-ITD) in patients with acute myeloid leukemia (AML) may depend on mutational burden and its interaction with other mutations. We analyzed the effect of FLT3-ITD/FLT3 wild-type (FLT3wt) ratio depending on NPM1 mutation (NPM1mut) in 303 patients with intermediate-risk cytogenetics AML treated with intensive chemotherapy. Among NPM1mut patients, FLT3wt and low ratio (<0.5) subgroups showed similar overall survival, relapse risk, and leukemia-free survival, whereas high ratio (≥0.5) patients had a worse outcome. In NPM1wt AML, FLT3-ITD subgroups showed a comparable outcome, with higher risk of relapse and shortened overall survival than FLT3wt patients. Allogeneic stem cell transplantation in CR1 was associated with a reduced relapse risk in all molecular subgroups with the exception of NPM1mut AML with absent or low ratio FLT3-ITD. In conclusion, effect of FLT3 burden is modulated by NPM1 mutation, especially in patients with a low ratio.

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عنوان ژورنال:
  • Blood

دوره 121 14  شماره 

صفحات  -

تاریخ انتشار 2013