Acute myeloid leukemia with NPM1 mutation and favorable European LeukemiaNet category: outcome after preemptive intervention based on measurable residual disease.

微小残留病 IDH2型 白血病 米多司他林
作者
Alex Bataller,Guadalupe Oñate,Marina Díaz-Beyá,Francesca Guijarro,Ana Garrido,Susana Vives,Mar Tormo,Montserrat Arnan,Olga Salamero,Antonia Sampol,Rosa Coll,Ferran Vall-Llovera,Aina Oliver-Caldés,Mónica López-Guerra,Marta Pratcorona,Lurdes Zamora,Eva Villamón,Gaël Roué,Adoración Blanco,Josep F. Nomdedeu,Dolors Colomer,Salut Brunet,Jorge Sierra,Jordi Esteve
出处
期刊:British Journal of Haematology [Wiley]
卷期号:191 (1): 52-61 被引量:9
标识
DOI:10.1111/bjh.16857
摘要

In the European LeukemiaNet favourable risk category, allogeneic haematopoietic stem cell transplantation (alloSCT) is not indicated in first complete remission for patients with acute myeloid leukaemia (AML) with NPM1 mutations (ELNfav NPM1 AML), although a proportion of these patients will relapse. Given the prognostic importance of measurable residual disease (MRD), CETLAM-12 considered a pre-emptive intervention in patients with molecular failure (MF). We analyzed 110 ELNfav NPM1 AML patients achieving complete remission (CR) after induction chemotherapy. Two-year cumulative incidence of relapse (CIR), overall survival (OS) and leukaemia-free survival (LFS) were 17%, 81·5% and 82%, respectively. Forty-six patients required additional therapy for MF (n = 33) or haematological relapse (HemR; n = 13), resulting in a molecular LFS (molLFS) and a cumulative incidence of MF at two years of 61% and 38% respectively. Two-year OS for these 46 patients was 66%, with a different outcome between patients with MF (86%) and HemR (42%) (P = 0·002). Quantitative NPM1 detection at different timepoints was predictive of molLFS; an MRD ratio (NPM1mut/ABL1 × 100) cut-off of 0·05 after first consolidation identified two cohorts with a two-year molLFS of 77% and 40% for patients below and above 0·05, respectively. In conclusion, MRD-based pre-emptive intervention resulted in a favourable outcome for ELNfav NPM1 AML patients.

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