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Validation of the revised IPSS at transplant in patients with myelodysplastic syndrome/transformed acute myelogenous leukemia receiving allogeneic stem cell transplantation: a retrospective analysis of the EBMT chronic malignancies working party.
Scheid, C; de Wreede, L; van Biezen, A; Koenecke, C; Göhring, G; Volin, L; Maertens, J; Finke, J; Passweg, J; Beelen, D; Cornelissen, J J; Itälä-Remes, M; Chevallier, P; Russell, N; Petersen, E; Milpied, N; Richard Espiga, C; Peniket, A; Sierra, J; Mufti, G; Crawley, C; Veelken, J H; Ljungman, P; Cahn, J Y; Alessandrino, E P; de Witte, T; Robin, M; Kröger, N.
Afiliação
  • Scheid C; Department of Medicine, University of Cologne, Cologne, Germany.
  • de Wreede L; Department of Medical Statistics and Bioinformatics, Leiden University Medical Center, Leiden, The Netherlands.
  • van Biezen A; DKMS, German Bone Marrow Donor Center, Dresden, Germany.
  • Koenecke C; Department of Medical Statistics and Bioinformatics, Leiden University Medical Center, Leiden, The Netherlands.
  • Göhring G; Department of Hematology, Hemostasis, Oncology and Stem Cell Transplantation, Hannover Medical School, Hannover, Germany.
  • Volin L; Institute of Cell and Molecular Pathology, Hannover Medical School, Hannover, Germany.
  • Maertens J; Stem Cell Transplantation Unit, HUCH Comprehensive Cancer Center, Helsinki, Finland.
  • Finke J; Department of Hematology, University Hospital Gasthuisberg, Leuven, Belgium.
  • Passweg J; Department of Medicine-Hematology, Oncology, University of Freiburg, Freiburg, Germany.
  • Beelen D; Hematology, University Hospital, Basel, Switzerland.
  • Cornelissen JJ; Department of Bone Marrow Transplantation, University Hospital, Essen, Germany.
  • Itälä-Remes M; Erasmus MC Cancer Institute, University Medical Center Rotterdam, Rotterdam, The Netherlands.
  • Chevallier P; TD7 (Stem Cell Transplant Unit), Turku University Hospital, Turku, Finland.
  • Russell N; Department D'Hematologie, CHU Nantes, Nantes, France.
  • Petersen E; Nottingham University, Nottingham, UK.
  • Milpied N; Department of Haematology, University Medical Centre, Utrecht, The Netherlands.
  • Richard Espiga C; CHU Bordeaux, Hôpital Haut-leveque, Pessac, France.
  • Peniket A; Servicio de Hematología-Hemoterapia, Hospital U. Marqués de Valdecilla, Santander, Spain.
  • Sierra J; Cancer and Haematology Centre, Churchill Hospital, Oxford, UK.
  • Mufti G; Hematology Department, Hospital Santa Creu i Sant Pau, Barcelona, Spain.
  • Crawley C; Department of Haematological Medicine, GKT School of Medicine, London, UK.
  • Veelken JH; Department of Haematology, Addenbrookes Hospital, Cambridge, UK.
  • Ljungman P; BMT Centre Leiden, Leiden University Hospital, Leiden, The Netherlands.
  • Cahn JY; Department of Hematology, Karolinska University Hospital, Stockholm, Sweden.
  • Alessandrino EP; Hématologie Clinique, Hopital A. Michallon, Grenoble, France.
  • de Witte T; Clinica Ematologica, Fondazione IRCCS Policlinico San Matteo, Pavia, Italy.
  • Robin M; Department of Hematology, Radboud University-Nijmegen Medical Centre, Nijmegen, The Netherlands.
  • Kröger N; Department of Hematology-BMT, Hopital St. Louis, Paris, France.
Bone Marrow Transplant ; 52(11): 1519-1525, 2017 Nov.
Article em En | MEDLINE | ID: mdl-28892084
ABSTRACT
The International Prognostic Scoring System has been revised (IPSS-R) to predict prognosis of patients with myelodysplastic syndromes at diagnosis. To validate the use of the IPSS-R assessed before transplant rather than at diagnosis we performed a retrospective analysis of the EBMT database. A total of 579 patients had sufficient information available to calculate IPSS-R at transplant. Median overall survival (OS) from transplant was significantly different according to IPSS-R very low 23.6 months, low 55.0 months, intermediate 19.7 months, high 13.5 months, very high 7.8 months (P<0.001). In a multivariate Cox model the following parameters were significant risk factors for OS IPSS-R, graft source, age and prior treatment. Median relapse free survival also showed significant differences according to IPSS-R very low 23.6 months, low 24.8 months, intermediate 10.6 months, high 7.9 months, very high 5.5 months (P<0.001). Multivariate risk factors for relapse-free survival (RFS) were IPSS-R, reduced intensity conditioning, graft source and prior treatment. A trend for an increased relapse incidence was noted for very high risk IPSS-R. We conclude that the IPSS-R at transplant is a useful prognostic score for predicting OS and RFS after transplantation, capturing both disease evolution and response to prior treatment before transplant.
Assuntos

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Prognóstico / Síndromes Mielodisplásicas / Leucemia Mieloide Aguda / Transplante de Células-Tronco Hematopoéticas Tipo de estudo: Etiology_studies / Observational_studies / Prognostic_studies / Risk_factors_studies Limite: Adolescent / Adult / Aged / Aged80 / Female / Humans / Male / Middle aged Idioma: En Revista: Bone Marrow Transplant Assunto da revista: TRANSPLANTE Ano de publicação: 2017 Tipo de documento: Article País de afiliação: Alemanha

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Prognóstico / Síndromes Mielodisplásicas / Leucemia Mieloide Aguda / Transplante de Células-Tronco Hematopoéticas Tipo de estudo: Etiology_studies / Observational_studies / Prognostic_studies / Risk_factors_studies Limite: Adolescent / Adult / Aged / Aged80 / Female / Humans / Male / Middle aged Idioma: En Revista: Bone Marrow Transplant Assunto da revista: TRANSPLANTE Ano de publicação: 2017 Tipo de documento: Article País de afiliação: Alemanha