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Long-term survival of patients with CLL after allogeneic transplantation: a report from the European Society for Blood and Marrow Transplantation.
van Gelder, M; de Wreede, L C; Bornhäuser, M; Niederwieser, D; Karas, M; Anderson, N S; Gramatzki, M; Dreger, P; Michallet, M; Petersen, E; Bunjes, D; Potter, M; Beelen, D; Cornelissen, J J; Yakoub-Agha, I; Russell, N H; Finke, J; Schoemans, H; Vitek, A; Urbano-Ispízua, Á; Blaise, D; Volin, L; Chevallier, P; Caballero, D; Putter, H; van Biezen, A; Henseler, A; Schönland, S; Kröger, N; Schetelig, J.
Afiliação
  • van Gelder M; Department of Internal Medicine/Hematology, University Hospital Maastricht, Maastricht, The Netherlands.
  • de Wreede LC; DKMS, gemeinnützige GmbH, Tübingen, Germany.
  • Bornhäuser M; Department of Medical Statistics and Bioinformatics, Leiden University Medical Center, Leiden, The Netherlands.
  • Niederwieser D; Medizinische Klinik und Poliklinik I, Universitätsklinikum Dresden, Technische Universität Dresden, Dresden, Germany.
  • Karas M; Division of Hematology, Oncology and Hemostasiology, University Hospital Leipzig, Leipzig, Germany.
  • Anderson NS; Department of Hematology/Oncology, Charles University Hospital, Pilsen, Czech Republic.
  • Gramatzki M; BMT Unit, Department of Hematology, Rigshospitalet, Copenhagen, Denmark.
  • Dreger P; Division of Stem Cell Transplantation and Immunotherapy, University Hospital Schleswig-Holstein, Kiel, Germany.
  • Michallet M; Medizinische Klinik und Poliklinik V, University of Heidelberg, Heidelberg, Germany.
  • Petersen E; Center Hospitalier Lyon-Sud - Hématologie, Lyon, France.
  • Bunjes D; Department of Haematology, University Medical Center, Utrecht, The Netherlands.
  • Potter M; Klinik fuer Innere Medizin III, Universitätsklinikum Ulm, Ulm, Germany.
  • Beelen D; Leukaemia Myeloma Units, Royal Marsden Hospital, London, Surrey, UK.
  • Cornelissen JJ; Department of Bone Marrow Transplantation, University Hospital, Essen, Germany.
  • Yakoub-Agha I; Erasmus MC-Daniel den Hoed Cancer Center, Rotterdam, The Netherlands.
  • Russell NH; Hôpital HURIEZ, UAM allo-CSH, CHRU, Lille, France.
  • Finke J; Nottingham City Hospital, Nottingham, UK.
  • Schoemans H; Department of Medicine-Hematology, Oncology, University of Freiburg, Freiburg, Germany.
  • Vitek A; Department of Hematology, University Hospital Gasthuisberg, Leuven, Belgium.
  • Urbano-Ispízua Á; Institute of Hematology and Blood Transfusion, Prague, Czech Republic.
  • Blaise D; Hospital Clinic, Institute of Hematology and Oncology, Department of Hematology, Barcelona, Spain.
  • Volin L; Programme de Transplantation and Therapie Cellulaire, Centre de Recherche en Cancérologie de Marseille, Institut Paoli Calmettes, Marseille, France.
  • Chevallier P; Stem Cell Transplantation Unit, Helsinki University Hospital Comprehensive Cancer Center, Helsinki, Finland.
  • Caballero D; Department D'Hematologie, CHU Nantes, Nantes, France.
  • Putter H; Servicio de Hematología, Hospital Clínico, Salamanca, Spain.
  • van Biezen A; Department of Medical Statistics and Bioinformatics, Leiden University Medical Center, Leiden, The Netherlands.
  • Henseler A; Department of Medical Statistics and Bioinformatics, Leiden University Medical Center, Leiden, The Netherlands.
  • Schönland S; Department of Medical Statistics and Bioinformatics, Leiden University Medical Center, Leiden, The Netherlands.
  • Kröger N; Medizinische Klinik und Poliklinik V, University of Heidelberg, Heidelberg, Germany.
  • Schetelig J; Bone Marrow Transplantation Center, University Hospital Eppendorf, Hamburg, Germany.
Bone Marrow Transplant ; 52(3): 372-380, 2017 Mar.
Article em En | MEDLINE | ID: mdl-27941763
Even with the availability of targeted drugs, allogeneic hematopoietic cell transplantation (allo-HCT) is the only therapy with curative potential for patients with CLL. Cure can be assessed by comparing long-term survival of patients to the matched general population. Using data from 2589 patients who received allo-HCT between 2000 and 2010, we used landmark analyses and methods from relative survival analysis to calculate excess mortality compared with an age-, sex- and calendar year-matched general population. Estimated event-free survival, overall survival and non-relapse mortality (NRM) 10 years after allo-HCT were 28% (95% confidence interval (CI), 25-31), 35% (95% CI, 32-38) and 40% (95% CI, 37-42), respectively. Patients who passed the 5-year landmark event-free survival (N=394) had a 79% probability (95% CI, 73-85) of surviving the subsequent 5 years without an event. Relapse and NRM contributed equally to treatment failure. Five-year mortality for 45- and 65-year-old reference patients who were event-free at the 5-year landmark was 8% and 47% compared with 3% and 14% in the matched general population, respectively. The prospect of long-term disease-free survival remains an argument to consider allo-HCT for young patients with high-risk CLL, and programs to understand and prevent late causes of failure for long-term survivors are warranted, especially for older patients.
Assuntos

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Leucemia Linfocítica Crônica de Células B / Transplante de Células-Tronco Hematopoéticas Tipo de estudo: Clinical_trials / Observational_studies / Prognostic_studies / Risk_factors_studies Limite: Adolescent / Adult / Aged / Child / Female / Humans / Male / Middle aged País/Região como assunto: Europa Idioma: En Ano de publicação: 2017 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Leucemia Linfocítica Crônica de Células B / Transplante de Células-Tronco Hematopoéticas Tipo de estudo: Clinical_trials / Observational_studies / Prognostic_studies / Risk_factors_studies Limite: Adolescent / Adult / Aged / Child / Female / Humans / Male / Middle aged País/Região como assunto: Europa Idioma: En Ano de publicação: 2017 Tipo de documento: Article