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Thiotepa-busulfan-fludarabine (TBF) conditioning regimen in patients undergoing allogeneic hematopoietic cell transplantation for myelofibrosis: an outcome analysis from the Chronic Malignancies Working Party of the EBMT.
Battipaglia, Giorgia; Mauff, Katya; Wendel, Lotus; Angelucci, Emanuele; Mohty, Mohamad; Arcese, William; Santarone, Stella; Rubio, Marie Therese; Kroger, Nicolaus; Fox, Maria Laura; Blaise, Didier; Iori, Anna Paola; Fanin, Renato; Chalandon, Yves; Pioltelli, Pietro; Marotta, Giuseppe; Chiusolo, Patrizia; Sever, Matjaz; Solano, Carlos; Contentin, Nathalie; de Wreede, Liesbeth C; Czerw, Tomasz; Hernandez-Boluda, Juan Carlos; Hayden, Patrick; McLornan, Donal; Yakoub-Agha, Ibrahim.
Afiliación
  • Battipaglia G; Department of Clinical Medicine and Surgery, Federico II University of Naples, Naples, Italy. giorgicchia@gmail.com.
  • Mauff K; EBMT Statistical Unit, Leiden, Netherlands.
  • Wendel L; EBMT Data Office, Leiden, Netherlands.
  • Angelucci E; IRCCS Ospedale Policlinico San Martino, Genova, Italy.
  • Mohty M; Department of Clinical Hematology and Cellular Therapy, Saint-Antoine Hospital, AP-HP, Sorbonne University, Paris, France.
  • Arcese W; Hematology, Stem Cell Transplant Unit, University Tor Vergata, Rome, Italy.
  • Santarone S; Ospedale Civile Dipartimento di Ematologia, Medicina Trasfusionale e Biotecnologie, Pescara, Italy.
  • Rubio MT; Department of Hematology, Hôpital Brabois, CHRU Nancy and CNRS UMR 7365, Biopole del'Université del Lorraine, Vendoeuvre les Nancy, France.
  • Kroger N; Department of Stem Cell Transplantation, Medical Center Hamburg-Eppendorf, Hamburg, Germany.
  • Fox ML; Department of Hematology, Vall d'Hebron Institute of Oncology (VHIO), University Hospital Vall d'Hebron, Barcelona, Spain.
  • Blaise D; Department of Hematology, Institut Paoli Calmettes, Marseille, France.
  • Iori AP; Hematology, Department of Translational and Precision Medicine, University Sapienza, Rome, Italy.
  • Fanin R; Division of Hematology and Stem Cell Transplantation, Azienda Sanitaria Universitaria Integrata di Udine, Udine, Italy.
  • Chalandon Y; Division of Hematology, University of Geneva Hospitals, Geneva, Switzerland.
  • Pioltelli P; Hematology Division and Bone Marrow Transplantation Unit, San Gerardo Hospital, Monza, Italy.
  • Marotta G; Department of Oncology, UOSA Transplant and Cellular Therapy Center, Azienda Ospedaliera Universitaria Senese, Siena, Italy.
  • Chiusolo P; Fondazione Policlinico A. Gemelli IRCCS, Roma, Italy.
  • Sever M; Istituto di Ematologia, Università Cattolica del Sacro Cuore, Roma, Italy.
  • Solano C; Department of Hematology, University Medical Centre Ljubljana, Ljubljana, Slovenia.
  • Contentin N; Faculty of Medicine, University of Ljubljana, Ljubljana, Slovenia.
  • de Wreede LC; Hematology Service, Hospital Clínico Universitario, INCLIVA Research Institute, Valencia, Spain.
  • Czerw T; Centre Henri Becquerel, Rouen, France.
  • Hernandez-Boluda JC; Department of Biomedical Data Sciences, Leiden University Medical Center, Leiden, The Netherlands.
  • Hayden P; Department of Bone Marrow Transplantation and Onco-Hematology, Maria Sklodowska-Curie National Research Institute of Oncology, Gliwice Branch, Poland.
  • McLornan D; Hematology Service, Hospital Clínico Universitario, INCLIVA Research Institute, Valencia, Spain.
  • Yakoub-Agha I; Department of Haematology, Trinity College Dublin, St. James's Hospital, Dublin, Ireland.
Bone Marrow Transplant ; 56(7): 1593-1602, 2021 07.
Article en En | MEDLINE | ID: mdl-33526919
ABSTRACT
Allogeneic hematopoietic cell transplantation (allo-HCT) remains the only curative option in MF. There is no consensus on the optimal conditioning regimen. We report outcomes of 187 patients with MF transplanted between 2010 and 2017 conditioned with TBF. Median age was 58 years. Median interval from diagnosis to allo-HCT was 44 months. Donors were haploidentical (41%), unrelated (36%) or HLA-identical siblings (23%). Stem cell source was PB in 60%. Conditioning was myeloablative in 48% of cases. Antithymocyte globulin (ATG) was used in 41% of patients. At 100 days, neutrophil and platelet engraftment were 91% and 63% after a median of 21 and 34 days, respectively. Grade II-IV and III-IV acute GVHD occurred in 24% and 12%, while at 3 years, all grade chronic GVHD and chronic extensive GVHD had been diagnosed in 38% and 11%. At 3 years, OS, RFS and GRFS were 55%, 49% and 43%, respectively. RI and NRM were 17% and 33%. On multivariate analysis, poor KPS and the use of unrelated donors were associated with worse GRFS and a higher grade II-IV acute GVHD, respectively. Neither donor type nor intensity of the conditioning regimen influenced survival outcomes. TBF is a feasible conditioning regimen in allo-HCT for MF in all donor settings although longer term outcomes are required.
Asunto(s)

Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Trasplante de Células Madre Hematopoyéticas / Mielofibrosis Primaria / Enfermedad Injerto contra Huésped / Neoplasias Tipo de estudio: Observational_studies / Risk_factors_studies Límite: Humans / Middle aged Idioma: En Revista: Bone Marrow Transplant Asunto de la revista: TRANSPLANTE Año: 2021 Tipo del documento: Article País de afiliación: Italia

Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Trasplante de Células Madre Hematopoyéticas / Mielofibrosis Primaria / Enfermedad Injerto contra Huésped / Neoplasias Tipo de estudio: Observational_studies / Risk_factors_studies Límite: Humans / Middle aged Idioma: En Revista: Bone Marrow Transplant Asunto de la revista: TRANSPLANTE Año: 2021 Tipo del documento: Article País de afiliación: Italia