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Comparative value of post-remission treatment in cytogenetically normal AML subclassified by NPM1 and FLT3-ITD allelic ratio.
Versluis, J; In 't Hout, F E M; Devillier, R; van Putten, W L J; Manz, M G; Vekemans, M-C; Legdeur, M-C; Passweg, J R; Maertens, J; Kuball, J; Biemond, B J; Valk, P J M; van der Reijden, B A; Meloni, G; Schouten, H C; Vellenga, E; Pabst, T; Willemze, R; Löwenberg, B; Ossenkoppele, G; Baron, F; Huls, G; Cornelissen, J J.
Afiliación
  • Versluis J; Department of Hematology, Erasmus University Medical Center Cancer Institute, Rotterdam, The Netherlands.
  • In 't Hout FE; Department of Hematology, Radboud University Medical Center, Nijmegen, The Netherlands.
  • Devillier R; Department of Laboratory medicine, Laboratory of Hematology, Radboud University Medical Center, Nijmegen, The Netherlands.
  • van Putten WL; Department of Hematology, Erasmus University Medical Center Cancer Institute, Rotterdam, The Netherlands.
  • Manz MG; HOVON Data Center, Erasmus University Medical Center Cancer Institute-Clinical Trial Center, Rotterdam, The Netherlands.
  • Vekemans MC; Division of Hematology, University Hospital Zürich, Zürich, Switzerland.
  • Legdeur MC; Department of Hematology, Hôpital St Luc, Brussels, Belgium.
  • Passweg JR; Department of Hematology, Medisch Spectrum Twente, Enschede, The Netherlands.
  • Maertens J; Stem Cell Transplant Team, University Hospital Basel, Basel, Switzerland.
  • Kuball J; Department of Hematology, University Hospital Gasthuisberg, Leuven, Belgium.
  • Biemond BJ; Department of Immunology and Hematology, University Medical Center, Utrecht, The Netherlands.
  • Valk PJ; Department of Hematology, Academic Medical Center, University of Amsterdam, Amsterdam, The Netherlands.
  • van der Reijden BA; Department of Hematology, Erasmus University Medical Center Cancer Institute, Rotterdam, The Netherlands.
  • Meloni G; Department of Laboratory medicine, Laboratory of Hematology, Radboud University Medical Center, Nijmegen, The Netherlands.
  • Schouten HC; Department of Cellular Biotechnologies and Hematology, 'Sapienza' University, Rome, Italy.
  • Vellenga E; Department of Hematology, University Hospital Maastricht, Maastricht, The Netherlands.
  • Pabst T; Department of Hematology, University Medical Center Groningen, Groningen, The Netherlands.
  • Willemze R; Department of Medical Oncology, Inselspital, Bern University Hospital, Bern, Switzerland.
  • Löwenberg B; Department of Hematology, Leiden University Medical Center, Leiden, The Netherlands.
  • Ossenkoppele G; Department of Hematology, Erasmus University Medical Center Cancer Institute, Rotterdam, The Netherlands.
  • Baron F; Department of Hematology, VU University Medical Center, Amsterdam, The Netherlands.
  • Huls G; Department of Hematology, University of Liège, Liège, Belgium.
  • Cornelissen JJ; Department of Hematology, Radboud University Medical Center, Nijmegen, The Netherlands.
Leukemia ; 31(1): 26-33, 2017 01.
Article en En | MEDLINE | ID: mdl-27416910
ABSTRACT
Post-remission treatment (PRT) in patients with cytogenetically normal (CN) acute myeloid leukemia (AML) in first complete remission (CR1) is debated. We studied 521 patients with CN-AML in CR1, for whom mutational status of NPM1 and FLT3-ITD was available, including the FLT3-ITD allelic ratio. PRT consisted of reduced intensity conditioning (RIC) allogeneic hematopoietic stem cell transplantation (alloHSCT) (n=68), myeloablative conditioning (MAC) alloHSCT (n=137), autologous hematopoietic stem cell transplantation (autoHSCT) (n=168) or chemotherapy (n=148). Favorable overall survival (OS) was found for patients with mutated NPM1 without FLT3-ITD (71±4%). Outcome in patients with a high FLT3-ITD allelic ratio appeared to be very poor with OS and relapse-free survival (RFS) of 23±8% and 12±6%, respectively. Patients with wild-type NPM1 without FLT3-ITD or with a low allelic burden of FLT3-ITD were considered as intermediate-risk group because of similar OS and RFS at 5 years, in which PRT by RIC alloHSCT resulted in better OS and RFS as compared with chemotherapy (hazard ratio (HR) 0.56, P=0.022 and HR 0.50, P=0.004, respectively) or autoHSCT (HR 0.60, P=0.046 and HR 0.60, P=0.043, respectively). The lowest cumulative incidence of relapse (23±4%) was observed following MAC alloHSCT. These results suggest that alloHSCT may be preferred in patients with molecularly intermediate-risk CN-AML, while the choice of conditioning type may be personalized according to risk for non-relapse mortality.
Asunto(s)

Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Proteínas Nucleares / Leucemia Mieloide Aguda / Trasplante de Células Madre Hematopoyéticas / Tirosina Quinasa 3 Similar a fms Tipo de estudio: Etiology_studies / Prognostic_studies / Risk_factors_studies Límite: Adolescent / Adult / Female / Humans / Male / Middle aged Idioma: En Revista: Leukemia Asunto de la revista: HEMATOLOGIA / NEOPLASIAS Año: 2017 Tipo del documento: Article País de afiliación: Países Bajos

Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Proteínas Nucleares / Leucemia Mieloide Aguda / Trasplante de Células Madre Hematopoyéticas / Tirosina Quinasa 3 Similar a fms Tipo de estudio: Etiology_studies / Prognostic_studies / Risk_factors_studies Límite: Adolescent / Adult / Female / Humans / Male / Middle aged Idioma: En Revista: Leukemia Asunto de la revista: HEMATOLOGIA / NEOPLASIAS Año: 2017 Tipo del documento: Article País de afiliación: Países Bajos