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

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...

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Detalles Bibliográficos
Autores: Bataller, A, Onate, G, Diaz-Beya, M, Guijarro, F, Garrido, A, Vives, S, Tormo, M, Arnan, M, Salamero, O, Sampol, A, Coll, R, Vall-Llovera, F, Oliver-Caldes, A, Lopez-Guerra, M, Pratcorona, M, Zamora, L, Villamon, E, Rou, G, Blanco, A, Nomdedeu, JF, Colomer, D, Brunet, S, Sierra, J, Esteve, J, Grp Cooperativo Estudio Tratamient
Tipo de recurso: artículo
Estado:Versión publicada
Fecha de publicación:2020
País:España
Institución:INCLIVA
Repositorio:r-INCLIVA. Repositorio Institucional de Producción Científica de INCLIVA
OAI Identifier:oai:incliva.fundanetsuite.com:p4585
Acceso en línea:https://incliva.portalinvestigacion.com/publicaciones/4585
Access Level:acceso abierto
Palabra clave:acute myeloid leukaemia
molecular analysis
stem cell transplantation
leukaemia
Descripción
Sumario: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 center dot 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 center dot 002). Quantitative NPM1 detection at different timepoints was predictive of molLFS; an MRD ratio (NPM1mut/ABL1 x 100) cut-off of 0 center dot 05 after first consolidation identified two cohorts with a two-year molLFS of 77% and 40% for patients below and above 0 center dot 05, respectively. In conclusion, MRD-based pre-emptive intervention resulted in a favourable outcome for ELNfav NPM1 AML patients.

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