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Survival improvement of patients with FLT3 mutated acute myeloid leukemia: results from a prospective 9 years cohort.
Oñate, Guadalupe; Pratcorona, Marta; Garrido, Ana; Artigas-Baleri, Alicia; Bataller, Alex; Tormo, Mar; Arnan, Montserrat; Vives, Susana; Coll, Rosa; Salamero, Olga; Vall-Llovera, Ferran; Sampol, Antònia; Garcia, Antoni; Cervera, Marta; Avila, Sara Garcia; Bargay, Joan; Ortín, Xavier; Nomdedéu, Josep F; Esteve, Jordi; Sierra, Jorge.
Affiliation
  • Oñate G; Hospital de la Santa Creu i Sant Pau. Institut d'investigació Biomèdica Sant Pau (IIB SANT PAU) Department of Medicine, Universitat Autonoma of Barcelona, Barcelona, Spain.
  • Pratcorona M; Hospital de la Santa Creu i Sant Pau. Institut d'investigació Biomèdica Sant Pau (IIB SANT PAU) Department of Medicine, Universitat Autonoma of Barcelona, Barcelona, Spain.
  • Garrido A; Hospital de la Santa Creu i Sant Pau. Institut d'investigació Biomèdica Sant Pau (IIB SANT PAU) Department of Medicine, Universitat Autonoma of Barcelona, Barcelona, Spain.
  • Artigas-Baleri A; Hospital de la Santa Creu i Sant Pau. Institut d'investigació Biomèdica Sant Pau (IIB SANT PAU) Department of Medicine, Universitat Autonoma of Barcelona, Barcelona, Spain.
  • Bataller A; Hospital Clinic. August Pi i Sunyer Biomedical Research Institute (IDIBAPS), University of Barcelona, Barcelona, Spain.
  • Tormo M; Hospital Clinico Universitario, Biomedical Research Institute INCLIVA, Valencia, Spain.
  • Arnan M; Institut Catala d'Oncologia, Hospital Duran i Reynals, Institut d'Investigacio Biomèdica de Bellvitge (IDIBELL), L'Hospitalet de Llobregat, University of Barcelona, Barcelona, Spain.
  • Vives S; Institut Catala d'Oncologia, Hospital Germans Trias i Pujol. Josep Carreras Leukemia Research Institute, Badalona, Universitat Autonoma of Barcelona, Barcelona, Spain.
  • Coll R; Institut Català d'Oncologia, Hospital Josep Trueta, Girona, Spain.
  • Salamero O; Hospital Universitari Vall d'Hebron and Institute of Oncology (VHIO), Universitat Autonoma of Barcelona, Barcelona, Spain.
  • Vall-Llovera F; Hospital Universitari Mutua de Terrassa, Barcelona, Spain.
  • Sampol A; Hospital Universitari Son Espases, Palma de Mallorca, Spain.
  • Garcia A; Hospital Arnau de Vilanova, Lleida, Spain.
  • Cervera M; Institut Catala d'Oncologia, Hospital Joan XXIII, Tarragona, Spain.
  • Avila SG; Hospital del Mar, Barcelona, Spain.
  • Bargay J; Hospital Son Llatzer, Palma de Mallorca, Spain.
  • Ortín X; Hospital Verge de la Cinta, Tortosa, Spain.
  • Nomdedéu JF; Hospital de la Santa Creu i Sant Pau. Institut d'investigació Biomèdica Sant Pau (IIB SANT PAU) Department of Medicine, Universitat Autonoma of Barcelona, Barcelona, Spain.
  • Esteve J; Hospital Clinic. August Pi i Sunyer Biomedical Research Institute (IDIBAPS), University of Barcelona, Barcelona, Spain.
  • Sierra J; Hospital de la Santa Creu i Sant Pau. Institut d'investigació Biomèdica Sant Pau (IIB SANT PAU) Department of Medicine, Universitat Autonoma of Barcelona, Barcelona, Spain. jsierra@santpau.cat.
Blood Cancer J ; 13(1): 69, 2023 05 05.
Article in En | MEDLINE | ID: mdl-37147301
ABSTRACT
Midostaurin added to intensive chemotherapy is the standard of care for acute myeloid leukemia (AML) with FLT3 mutations (FLT3mut). We analyzed the impact of midostaurin in 227 FLT3mut-AML patients included in the AML-12 prospective trial for fit patients ≤70 years (#NCT04687098). Patients were divided into an early (2012-2015) and late (2016-2020) cohorts. They were uniformly treated except for the addition of midostaurin in 71% of late group patients. No differences were observed in response rates or the number of allotransplants between groups. Outcome was improved in the late period 2-year relapse incidence decreased from 42% vs 29% in early vs late group (p = 0.024) and 2-year overall survival (OS) improved from 47% vs 61% (p = 0.042), respectively. The effect of midostaurin was evident in NPM1mut patients (n = 151), with 2-yr OS of 72% (exposed) vs 50% (naive) patients (p = 0.011) and mitigated FLT3-ITD allelic ratio prognostic value 2-yr OS with midostaurin was 85% and 58% in low and high ratio patients (p = 0.049) vs 67% and 39% in naive patients (p = 0.005). In the wild-type NPM1 subset (n = 75), we did not observe significant differences between both study periods. In conclusion, this study highlights the improved outcome of FLT3mut AML fit patients with the incorporation of midostaurin.
Subject(s)

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Leukemia, Myeloid, Acute / Nucleophosmin Type of study: Observational_studies / Prognostic_studies / Risk_factors_studies Limits: Humans Language: En Journal: Blood Cancer J Year: 2023 Document type: Article Affiliation country: España

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Leukemia, Myeloid, Acute / Nucleophosmin Type of study: Observational_studies / Prognostic_studies / Risk_factors_studies Limits: Humans Language: En Journal: Blood Cancer J Year: 2023 Document type: Article Affiliation country: España