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Acute myeloid leukemia with NPM1 mutation and favorable European LeukemiaNet category: outcome after preemptive intervention based on measurable residual disease.
Bataller, Alex; Oñate, Guadalupe; Diaz-Beyá, Marina; Guijarro, Francesca; Garrido, Ana; Vives, Susana; Tormo, Mar; Arnan, Montserrat; Salamero, Olga; Sampol, Antònia; Coll, Rosa; Vall-Llovera, Ferran; Oliver-Caldés, Aina; López-Guerra, Mònica; Pratcorona, Marta; Zamora, Lurdes; Villamon, Eva; Roué, Gaël; Blanco, Adoración; Nomdedeu, Josep F; Colomer, Dolors; Brunet, Salut; Sierra, Jorge; Esteve, Jordi.
Afiliação
  • Bataller A; Hematology Department, Hospital Clínic de Barcelona, IDIBAPS, University of Barcelona, Barcelona, Spain.
  • Oñate G; Hematology Department, Hospital de la Santa Creu i Sant Pau, UAB, Barcelona, Spain.
  • Diaz-Beyá M; Hematology Department, Hospital Clínic de Barcelona, IDIBAPS, University of Barcelona, Barcelona, Spain.
  • Guijarro F; Hematology Department, Hospital Clínic de Barcelona, IDIBAPS, University of Barcelona, Barcelona, Spain.
  • Garrido A; Hematology Department, Hospital de la Santa Creu i Sant Pau, UAB, Barcelona, Spain.
  • Vives S; Hematology Department, ICO - Hospital Germans Trias i Pujol, Badalona, Spain.
  • Tormo M; Hematology Department, Hospital Clínico Universitario de Valencia, Valencia, Spain.
  • Arnan M; Hematology Department, ICO - Hospital Duran i Reynals, L'Hospitalet de Llobregat, Barcelona, Spain.
  • Salamero O; Hematology Department, Hospital Universitari Vall d'Hebron, Barcelona, Spain.
  • Sampol A; Hematology Department, Hospital Universitari Son Espases, Palma de Mallorca, Spain.
  • Coll R; Hematology Department, ICO - Hospital Universitari Dr. Josep Trueta, Girona, Spain.
  • Vall-Llovera F; Hematology Department, Hospital Universitari Mútua de Terrassa, Terrassa, Spain.
  • Oliver-Caldés A; Hematology Department, Hospital Clínic de Barcelona, IDIBAPS, University of Barcelona, Barcelona, Spain.
  • López-Guerra M; Hematopathology Section, Hospital Clínic, IDIBAPS, CIBERONC, UB, Barcelona, Spain.
  • Pratcorona M; Hematology Department, Hospital de la Santa Creu i Sant Pau, UAB, Barcelona, Spain.
  • Zamora L; Hematology Department, ICO - Hospital Germans Trias i Pujol, Badalona, Spain.
  • Villamon E; Hematology Department, Hospital Clínico Universitario de Valencia, Valencia, Spain.
  • Roué G; Hematology Department, Hospital Universitari Vall d'Hebron, Barcelona, Spain.
  • Blanco A; Hematology Department, Hospital Universitari Vall d'Hebron, Barcelona, Spain.
  • Nomdedeu JF; Hematology Department, Hospital de la Santa Creu i Sant Pau, UAB, Barcelona, Spain.
  • Colomer D; Hematopathology Section, Hospital Clínic, IDIBAPS, CIBERONC, UB, Barcelona, Spain.
  • Brunet S; Hematology Department, Hospital de la Santa Creu i Sant Pau, UAB, Barcelona, Spain.
  • Sierra J; Hematology Department, Hospital de la Santa Creu i Sant Pau, UAB, Barcelona, Spain.
  • Esteve J; Hematology Department, Hospital Clínic de Barcelona, IDIBAPS, University of Barcelona, Barcelona, Spain.
Br J Haematol ; 191(1): 52-61, 2020 10.
Article em En | MEDLINE | ID: mdl-32510599
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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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Proteínas Nucleares / Leucemia Mieloide Aguda / Quimioterapia de Indução / Mutação / Proteínas de Neoplasias Tipo de estudo: Prognostic_studies Limite: Adolescent / Adult / Aged / Female / Humans / Male / Middle aged País como assunto: Europa Idioma: En Ano de publicação: 2020 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Proteínas Nucleares / Leucemia Mieloide Aguda / Quimioterapia de Indução / Mutação / Proteínas de Neoplasias Tipo de estudo: Prognostic_studies Limite: Adolescent / Adult / Aged / Female / Humans / Male / Middle aged País como assunto: Europa Idioma: En Ano de publicação: 2020 Tipo de documento: Article