| Literature DB >> 32510599 |
Alex Bataller1, Guadalupe Oñate2, Marina Diaz-Beyá1, Francesca Guijarro1, Ana Garrido2, Susana Vives3, Mar Tormo4, Montserrat Arnan5, Olga Salamero6, Antònia Sampol7, Rosa Coll8, Ferran Vall-Llovera9, Aina Oliver-Caldés1, Mònica López-Guerra10, Marta Pratcorona2, Lurdes Zamora3, Eva Villamon4, Gaël Roué6, Adoración Blanco6, Josep F Nomdedeu2, Dolors Colomer10, Salut Brunet2, Jorge Sierra2, Jordi Esteve1.
Abstract
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.Entities:
Keywords: acute myeloid leukaemia; leukaemia; molecular analysis; stem cell transplantation
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Year: 2020 PMID: 32510599 DOI: 10.1111/bjh.16857
Source DB: PubMed Journal: Br J Haematol ISSN: 0007-1048 Impact factor: 6.998