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European LeukemiaNet 2017 risk stratification for acute myeloid leukemia: validation in a risk-adapted protocol.
Bataller, Alex; Garrido, Ana; Guijarro, Francesca; Oñate, Guadalupe; Diaz-Beyá, Marina; Arnan, Montserrat; Tormo, Mar; Vives, Susana; de Llano, María Paz Queipo; Coll, Rosa; Gallardo, David; Vall-Llovera, Ferran; Escoda, Lourdes; Garcia-Guiñon, Antonio; Salamero, Olga; Sampol, Antònia; Merchan, Brayan M; Bargay, Joan; Castaño-Díez, Sandra; Esteban, Daniel; Oliver-Caldés, Aina; Rivero, Andrea; Mozas, Pablo; López-Guerra, Mònica; Pratcorona, Marta; Zamora, Lurdes; Costa, Dolors; Rozman, Maria; Nomdedéu, Josep F; Colomer, Dolors; Brunet, Salut; Sierra, Jorge; Esteve, Jordi.
Afiliación
  • Bataller A; Hematology Department, Hospital Clínic de Barcelona, August Pi i Sunyer Biomedical Research Institute (IDIBAPS), University of Barcelona (UB), Barcelona, Spain.
  • Garrido A; Josep Carreras Leukemia Research Institute, Barcelona, Spain.
  • Guijarro F; Josep Carreras Leukemia Research Institute, Barcelona, Spain.
  • Oñate G; Hematology Department, Hospital de la Santa Creu i Sant Pau, Universitat Autònoma de Barcelona (UAB), Barcelona, Spain.
  • Diaz-Beyá M; Hematology Department, Hospital Clínic de Barcelona, August Pi i Sunyer Biomedical Research Institute (IDIBAPS), University of Barcelona (UB), Barcelona, Spain.
  • Arnan M; Josep Carreras Leukemia Research Institute, Barcelona, Spain.
  • Tormo M; Hematology Department, Hospital de la Santa Creu i Sant Pau, Universitat Autònoma de Barcelona (UAB), Barcelona, Spain.
  • Vives S; Hematology Department, Hospital Clínic de Barcelona, August Pi i Sunyer Biomedical Research Institute (IDIBAPS), University of Barcelona (UB), Barcelona, Spain.
  • de Llano MPQ; Hematology Department, Catalan Institute of Oncology (ICO)-Hospital Duran i Reynals, L'Hospitalet de Llobregat, Spain.
  • Coll R; Hematology Department, Hospital Clínico Universitario de Valencia, Valencia, Spain.
  • Gallardo D; Hematology Department, Catalan Institute of Oncology (ICO)-Hospital Germans Trias i Pujol, Badalona, Spain.
  • Vall-Llovera F; Hematology Department, Hospital Virgen de la Victoria, Málaga, Spain.
  • Escoda L; Hematology Department, Catalan Institute of Oncology (ICO)-Hospital Universitari Dr. Josep Trueta, Girona, Spain.
  • Garcia-Guiñon A; Hematology Department, Catalan Institute of Oncology (ICO)-Hospital Universitari Dr. Josep Trueta, Girona, Spain.
  • Salamero O; Hematology Department, Hospital Universitari Mútua de Terrassa, Terrassa, Spain.
  • Sampol A; Hematology Department, Catalan Institute of Oncology (ICO)-Hospital Universitari Joan XXIII, Tarragona, Spain.
  • Merchan BM; Hematology Department, Hospital Arnau de Vilanova, Lleida, Spain.
  • Bargay J; Hematology Department, Hospital Universitari Vall d'Hebron, Barcelona, Spain.
  • Castaño-Díez S; Hematology Department, Hospital Universitari Son Espases, Palma de Mallorca, Spain.
  • Esteban D; Hematology Department, Hospital del Mar, Barcelona, Spain.
  • Oliver-Caldés A; Hematology Department, Hospital Universitari Son Llàtzer, Palma de Mallorca, Spain.
  • Rivero A; Hematology Department, Hospital Clínic de Barcelona, August Pi i Sunyer Biomedical Research Institute (IDIBAPS), University of Barcelona (UB), Barcelona, Spain.
  • Mozas P; Hematology Department, Hospital Clínic de Barcelona, August Pi i Sunyer Biomedical Research Institute (IDIBAPS), University of Barcelona (UB), Barcelona, Spain.
  • López-Guerra M; Hematology Department, Hospital Clínic de Barcelona, August Pi i Sunyer Biomedical Research Institute (IDIBAPS), University of Barcelona (UB), Barcelona, Spain.
  • Pratcorona M; Hematology Department, Hospital Clínic de Barcelona, August Pi i Sunyer Biomedical Research Institute (IDIBAPS), University of Barcelona (UB), Barcelona, Spain.
  • Zamora L; Hematology Department, Hospital Clínic de Barcelona, August Pi i Sunyer Biomedical Research Institute (IDIBAPS), University of Barcelona (UB), Barcelona, Spain.
  • Costa D; Hematopathology Section, Hospital Clínic de Barcelona, August Pi i Sunyer Biomedical Research Institute (IDIBAPS), University of Barcelona (UB), Barcelona, Spain; and.
  • Rozman M; Centro de Investigación Biomédica en Red en Oncología, Madrid, Spain.
  • Nomdedéu JF; Josep Carreras Leukemia Research Institute, Barcelona, Spain.
  • Colomer D; Hematology Department, Hospital de la Santa Creu i Sant Pau, Universitat Autònoma de Barcelona (UAB), Barcelona, Spain.
  • Brunet S; Josep Carreras Leukemia Research Institute, Barcelona, Spain.
  • Sierra J; Hematology Department, Catalan Institute of Oncology (ICO)-Hospital Germans Trias i Pujol, Badalona, Spain.
  • Esteve J; Hematopathology Section, Hospital Clínic de Barcelona, August Pi i Sunyer Biomedical Research Institute (IDIBAPS), University of Barcelona (UB), Barcelona, Spain; and.
Blood Adv ; 6(4): 1193-1206, 2022 02 22.
Article en En | MEDLINE | ID: mdl-34911079
ABSTRACT
The 2017 European LeukemiaNet (ELN 2017) guidelines for the diagnosis and management of acute myeloid leukemia (AML) have become fundamental guidelines to assess the prognosis and postremission therapy of patients. However, they have been retrospectively validated in few studies with patients included in different treatment protocols. We analyzed 861 patients included in the Cooperativo Para el Estudio y Tratamiento de las Leucemias Agudas y Mielodisplasias-12 risk-adapted protocol, which indicates cytarabine-based consolidation for patients allocated to the ELN 2017 favorable-risk group, whereas it recommends allogeneic stem cell transplantation (alloSCT) as a postremission strategy for the ELN 2017 intermediate- and adverse-risk groups. We retrospectively classified patients according to the ELN 2017, with 327 (48%), 109 (16%), and 245 (36%) patients allocated to the favorable-, intermediate-, and adverse-risk group, respectively. The 2- and 5-year overall survival (OS) rates were 77% and 70% for favorable-risk patients, 52% and 46% for intermediate-risk patients, and 33% and 23% for adverse-risk patients, respectively. Furthermore, we identified a subgroup of patients within the adverse group (inv(3)/t(3;3), complex karyotype, and/or TP53 mutation/17p abnormality) with a particularly poor outcome, with a 2-year OS of 15%. Our study validates the ELN 2017 risk stratification in a large cohort of patients treated with an ELN-2017 risk-adapted protocol based on alloSCT after remission for nonfavorable ELN subgroups and identifies a genetic subset with a very poor outcome that warrants investigation of novel strategies.
Asunto(s)

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Leucemia Mieloide Aguda / Trasplante de Células Madre Hematopoyéticas Tipo de estudio: Diagnostic_studies / Etiology_studies / Guideline / Observational_studies / Prognostic_studies / Risk_factors_studies Límite: Humans Idioma: En Revista: Blood Adv Año: 2022 Tipo del documento: Article País de afiliación: España

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Leucemia Mieloide Aguda / Trasplante de Células Madre Hematopoyéticas Tipo de estudio: Diagnostic_studies / Etiology_studies / Guideline / Observational_studies / Prognostic_studies / Risk_factors_studies Límite: Humans Idioma: En Revista: Blood Adv Año: 2022 Tipo del documento: Article País de afiliación: España