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Trends in allogeneic haematopoietic cell transplantation for myelofibrosis in Europe between 1995 and 2018: a CMWP of EBMT retrospective analysis.
McLornan, D; Eikema, D J; Czerw, T; Kröger, N; Koster, L; Reinhardt, Hans Christian; Angelucci, E; Robin, M; Bornhäuser, M; Passweg, J; Clark, A; Vydra, J; Blau, I E; Niittyvuopio, R; Platzbecker, U; Cornelissen, J J; Chevallier, P; Srour, M; Stamatovic, D; Martinez-Lopez, J; de Wreede, L; Hayden, P; Hernández-Boluda, J C; Yakoub-Agha, I.
Afiliação
  • McLornan D; Department of Haematology, Guy's and St. Thomas' NHS Foundation Trust and University College Hospital, London, UK. donal.mclornan@nhs.net.
  • Eikema DJ; Department of Medical Statistics, Leiden University Medical Centre, Leiden, The Netherlands.
  • Czerw T; Maria Sklodowska-Curie Memorial Cencer Center and Institute of Oncology Gliwice Branch, Gliwice, Poland.
  • Kröger N; Division of Stem Cell Transplantation, University Hospital Eppendorf, Hamburg, Germany.
  • Koster L; EBMT Data Office, Leiden, The Netherlands.
  • Reinhardt HC; Department of Hematology and Stem Cell Transplantation, West German Cancer Center University Hospital Essen, Essen, Germany.
  • Angelucci E; Hematologia and Transplant Center, IRCCS Ospedale Policlinico San Martino, Genova, Italy.
  • Robin M; Hôpital Saint-Louis, Service d'Hématologie-Greffe, Assistance Publique Hôpitaux de Paris, Paris, France.
  • Bornhäuser M; Universitaetsklinikum Dresden, Dresden, Germany.
  • Passweg J; Klinik für Hämatologie,Bereich Innere Medizin, Universitätsspital Basel, Basel, Switzerland.
  • Clark A; Department of Haematology and Stem Cell Transplant, Beatson Centre, Glasgow, Scotland.
  • Vydra J; Institute of Hematology and Blood Transfusion, Prague, Czech Republic.
  • Blau IE; Charité Universitätsmedizin Berlin, Berlin, Germany.
  • Niittyvuopio R; HUCH Comprehensive Cancer Center, Helsinki, Finland.
  • Platzbecker U; University Hospital Leipzig, Leipzig, Germany.
  • Cornelissen JJ; Department of Haematology, Erasmus MC/Daniel den Hoed Cancer Center, Rottrdam, The Netherlands.
  • Chevallier P; CHU Nantes, Nantes, France.
  • Srour M; Centre Hospitalier Régional Universitaire de Lille, Hospital Claude Huriez, Huriez, France.
  • Stamatovic D; Department of Haematology, Military Medical Academy, Belgrade, Serbia.
  • Martinez-Lopez J; Hospital Universitario 12 de Octubre, Avd de Cordoba s/n, Madrid, Spain.
  • de Wreede L; Department of Medical Statistics, Leiden University Medical Centre, Leiden, The Netherlands.
  • Hayden P; Department of Haematology, St.James Hospital, Dublin, Ireland.
  • Hernández-Boluda JC; Hospital Clínico Universitario de Valencia, Valencia, Spain.
  • Yakoub-Agha I; Service des Maladies du Sang, CHRU de Lille, LIRIC, INSERM U995, Universite de Lille, Lille, France. ibrahim.yakoubagha@chru-lille.fr.
Bone Marrow Transplant ; 56(9): 2160-2172, 2021 09.
Article em En | MEDLINE | ID: mdl-33911203
ABSTRACT
We performed a retrospective assessment of patient- and transplant-specific characteristics and outcomes for 4142 patients undergoing allogeneic haematopoietic cell transplant for myelofibrosis between 1995 and 2018 across 278 centres. Activity increased steadily across the four analysed eras (<2006, 2006-2010, 2011-2014 and 2015-2018). Median recipient age increased over time between the earliest and most recent cohort (49.4 years (range, 20.1-68) versus 59.3 years (range, 18.1-78.1). Increasing number of patients with a Karnofsky performance status <90 underwent transplant over time. Increased utilisation of matched unrelated donors was apparent (<2006, 22.5% versus 2015-18, 45.2%; p < 0.001). Decreased use of myeloablative conditioning, increased use of busulphan-based platforms and anti-thymocyte globulin was evident. Of note, rates of acute (a)GVHD grade II-IV by day +100 decreased over time (p = 0.027) as did rates of chronic (c) GVHD, predominantly extensive cGVHD (<2006, 36% (31-41%) versus 2015-18, 23% (21-25%); p = 0.001). Overall, significant factors associated with worse overall survival and non-relapse mortality (NRM) remained older age, use of donors other than matched sibling, recipient CMV seropositivity and a lower Karnofsky performance status (<90). Multivariable analysis demonstrated improvements in overall survival and reductions in relapse risk over time with stable NRM rates despite increasing numbers of older, less fit patients and use of unrelated donors.
Assuntos

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Transplante de Células-Tronco Hematopoéticas / Mielofibrose Primária / Doença Enxerto-Hospedeiro Tipo de estudo: Observational_studies Limite: Adult / Aged / Humans / Middle aged Idioma: En Ano de publicação: 2021 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Transplante de Células-Tronco Hematopoéticas / Mielofibrose Primária / Doença Enxerto-Hospedeiro Tipo de estudo: Observational_studies Limite: Adult / Aged / Humans / Middle aged Idioma: En Ano de publicação: 2021 Tipo de documento: Article