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Comparative therapeutic value of post-remission approaches in patients with acute myeloid leukemia aged 40-60 years.
Cornelissen, J J; Versluis, J; Passweg, J R; van Putten, W L J; Manz, M G; Maertens, J; Beverloo, H B; Valk, P J M; van Marwijk Kooy, M; Wijermans, P W; Schaafsma, M R; Biemond, B J; Vekemans, M-C; Breems, D A; Verdonck, L F; Fey, M F; Jongen-Lavrencic, M; Janssen, J J W M; Huls, G; Kuball, J; Pabst, T; Graux, C; Schouten, H C; Gratwohl, A; Vellenga, E; Ossenkoppele, G; Löwenberg, B.
Afiliação
  • Cornelissen JJ; Department of Hematology, Erasmus University medical center Cancer Institute, Rotterdam, The Netherlands.
  • Versluis J; Department of Hematology, Erasmus University medical center Cancer Institute, Rotterdam, The Netherlands.
  • Passweg JR; Stem Cell Transplant Team, University Hospital Basel, Basel, Switzerland.
  • van Putten WL; HOVON Data Center and Department of Trials and Statistics, Rotterdam, The Netherlands.
  • Manz MG; Division of Hematology, University Hospital Zürich, Zürich, Switzerland.
  • Maertens J; Department of Hematology, University Hospital Gasthuisberg, Leuven, Belgium.
  • Beverloo HB; Department of Clinical Genetics, Erasmus University Medical Center Rotterdam, Rotterdam, The Netherlands.
  • Valk PJ; Department of Hematology, Erasmus University medical center Cancer Institute, Rotterdam, The Netherlands.
  • van Marwijk Kooy M; Department of Internal medicine, Isala Hospital, Zwolle, The Netherlands.
  • Wijermans PW; Department of Hematology, Haga Hospital, The Hague, The Netherlands.
  • Schaafsma MR; Department of Hematology, Medisch Spectrum Twente, Enschede, The Netherlands.
  • Biemond BJ; Department of Hematology, Academic Medical Center, University of Amsterdam, Amsterdam, The Netherlands.
  • Vekemans MC; Department of Hematology, Hôpital St Luc, Brussels, Belgium.
  • Breems DA; Department of Hematology, Stuivenberg Hospital, Antwerp, Belgium.
  • Verdonck LF; Departments of Immunology and Hematology, University Medical Center, Utrecht, The Netherlands.
  • Fey MF; Department of Medical Oncology, Inselspital, Bern University Hospital, Bern, Switzerland.
  • Jongen-Lavrencic M; Department of Hematology, Erasmus University medical center Cancer Institute, Rotterdam, The Netherlands.
  • Janssen JJ; Department of Hematology, VU University Medical Center, Amsterdam, The Netherlands.
  • Huls G; Department of Hematology, University Medical Center Groningen, Groningen, The Netherlands.
  • Kuball J; Departments of Immunology and Hematology, University Medical Center, Utrecht, The Netherlands.
  • Pabst T; Department of Medical Oncology, Inselspital, Bern University Hospital, Bern, Switzerland.
  • Graux C; Department of Hematology, Mont-Godinne, Yvoir, Belgium.
  • Schouten HC; Department of Hematology, University Hospital Maastricht, Maastricht, The Netherlands.
  • Gratwohl A; Stem Cell Transplant Team, University Hospital Basel, Basel, Switzerland.
  • Vellenga E; Department of Hematology, University Medical Center Groningen, Groningen, The Netherlands.
  • Ossenkoppele G; Department of Hematology, VU University Medical Center, Amsterdam, The Netherlands.
  • Löwenberg B; Department of Hematology, Erasmus University medical center Cancer Institute, Rotterdam, The Netherlands.
Leukemia ; 29(5): 1041-50, 2015 May.
Article em En | MEDLINE | ID: mdl-25428261
ABSTRACT
The preferred type of post-remission therapy (PRT) in patients with acute myeloid leukemia (AML) in first complete remission (CR1) is a subject of continued debate, especially in patients at higher risk of nonrelapse mortality (NRM), including patients >40 years of age. We report results of a time-dependent multivariable analysis of allogenic hematopoietic stem cell transplantation (alloHSCT) (n=337) versus chemotherapy (n=271) or autologous HSCT (autoHSCT) (n=152) in 760 patients aged 40-60 years with AML in CR1. Patients receiving alloHSCT showed improved overall survival (OS) as compared with chemotherapy (respectively, 57±3% vs 40±3% at 5 years, P<0.001). Comparable OS was observed following alloHSCT and autoHSCT in patients with intermediate-risk AML (60±4 vs 54±5%). However, alloHSCT was associated with less relapse (hazard ratio (HR) 0.51, P<0.001) and better relapse-free survival (RFS) (HR 0.74, P=0.029) as compared with autoHSCT in intermediate-risk AMLs. AlloHSCT was applied following myeloablative conditioning (n=157) or reduced intensity conditioning (n=180), resulting in less NRM, but comparable outcome with respect to OS, RFS and relapse. Collectively, these results show that alloHSCT is to be preferred over chemotherapy as PRT in patients with intermediate- and poor-risk AML aged 40-60 years, whereas autoHSCT remains a treatment option to be considered in patients with intermediate-risk AML.
Assuntos

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Leucemia Mieloide Aguda Tipo de estudo: Etiology_studies / Prognostic_studies / Risk_factors_studies Limite: Adult / Female / Humans / Male / Middle aged Idioma: En Revista: Leukemia Assunto da revista: HEMATOLOGIA / NEOPLASIAS Ano de publicação: 2015 Tipo de documento: Article País de afiliação: Holanda

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Leucemia Mieloide Aguda Tipo de estudo: Etiology_studies / Prognostic_studies / Risk_factors_studies Limite: Adult / Female / Humans / Male / Middle aged Idioma: En Revista: Leukemia Assunto da revista: HEMATOLOGIA / NEOPLASIAS Ano de publicação: 2015 Tipo de documento: Article País de afiliação: Holanda