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Alternative donor transplantation for severe aplastic anemia: a comparative study of the SAAWP EBMT.
Montoro, Juan; Eikema, Dirk-Jan; Tuffnell, Joe; Potter, Victoria; Kalwak, Krzysztof; Halkes, Constantijn J M; Kulagin, Alexander; Collin, Matthew; Wynn, Robert F; Robinson, Stephen; Nicholson, Emma; Sengeloev, Henrik; Clay, Jennifer; Halahleh, Khalid; Skorobogatova, Elena; Sanz, Jaime; Passweg, Jakob; Mielke, Stephan; Ryhänen, Samppa; Carpenter, Ben; Gedde-Dahl, Tobias; Tholouli, Eleni; Fanin, Renato; Lewalle, Philippe; Kulasekararaj, Austin; Risitano, Antonio; Peffault de Latour, Régis.
Afiliación
  • Montoro J; Department of Hematology, Hospital Universitario y Politécnico La Fe, Valencia, Valencia, Spain.
  • Eikema DJ; Universidad Católica de Valencia, Valencia, Spain.
  • Tuffnell J; EBMT Leiden Study Unit, Leiden, The Netherlands.
  • Potter V; EBMT Leiden Study Unit, Leiden, The Netherlands.
  • Kalwak K; Department of Haematological Medicine, Kings College Hospital, London, United Kingdom.
  • Halkes CJM; Fundacja Na Ratunek Dzieciom z Choroba Nowotworowa, Wroclaw, Poland.
  • Kulagin A; Leiden University Hospital, Leiden, The Netherlands.
  • Collin M; RM Gorbacheva Research Institute, Pavlov University, St. Petersburg, Russia.
  • Wynn RF; Northern Centre for Bone Marrow Transplantation, Newcastle, United Kingdom.
  • Robinson S; Royal Manchester Children's Hospital, Manchester, United Kingdom.
  • Nicholson E; Bristol Royal Hospital for Children, Bristol, United Kingdom.
  • Sengeloev H; Royal Marsden Hospital, London, United Kingdom.
  • Clay J; Rigshospitalet, Copenhagen, Denmark.
  • Halahleh K; Yorkshire Blood and Marrow Transplant Programme, Leeds, United Kingdom.
  • Skorobogatova E; King Hussein Cancer Centre Adult Blood and Bone Marrow Transplantation Program, Amman, Jordan.
  • Sanz J; The Russian Federation Children's Research Hospital, Moscow, Russia.
  • Passweg J; Department of Hematology, Hospital Universitario y Politécnico La Fe, Valencia, Valencia, Spain.
  • Mielke S; University Hospital Basel, Basel, Switzerland.
  • Ryhänen S; Karolinska Institute and University Hospital, Stockholm, Sweden.
  • Carpenter B; Hospital for Children and Adolescent, University of Helsinki, Helsinki, Finland.
  • Gedde-Dahl T; University College London Hospital, London, United Kingdom.
  • Tholouli E; Oslo University Hospital, Rikshospitalet, Oslo, Norway.
  • Fanin R; Manchester Royal Infirmary, Manchester, United Kingdom.
  • Lewalle P; Azienda Ospedaliero Universitaria di Udine, Udine, Italy.
  • Kulasekararaj A; Institut Jules Bordet, Brussels, Belgium.
  • Risitano A; Department of Haematological Medicine, Kings College Hospital, London, United Kingdom.
  • Peffault de Latour R; University of Naples, Avellino, Italy.
Blood ; 144(3): 323-333, 2024 Jul 18.
Article en En | MEDLINE | ID: mdl-38643511
ABSTRACT
ABSTRACT Selecting the most suitable alternative donor becomes challenging in severe aplastic anemia (SAA) when a matched sibling donor (MSD) is unavailable. We compared outcomes in patients with SAA undergoing stem cell transplantation (SCT) from matched unrelated donors (MUD) (n = 1106), mismatched unrelated donors (MMUD) (n = 340), and haploidentical donors (Haplo) (n = 206) registered in the European Society for Blood and Marrow Transplantation database (2012-2021). For Haplo SCT, only those receiving posttransplant cyclophosphamide for graft-versus-host disease (GVHD) prophylaxis were included. Median age was 20 years, and the median time from diagnosis to transplantation 8.7 months. Compared with MUD, MMUD (hazard ratio [HR], 2.93; 95% confidence interval [CI], 1.52-5.6) and Haplo (HR, 5.15; 95% CI, 2.5-10.58) showed significantly higher risks of primary graft failure. MUD had lower rates of acute GVHD compared with MMUD and Haplo (grade 2-4 13%, 22%, and 19%, respectively; P < .001; grade 3-4 5%, 9%, and 7%, respectively; P = .028). The 3-year nonrelapse mortality rate was 14% for MUD, 19% for MMUD, and 27% for Haplo (P < .001), whereas overall survival and GVHD and relapse-free survival (GRFS) rates were 81% and 73% for MUD, 74% and 65% for MMUD, and 63% and 54% for Haplo, respectively (P < .001). In addition to donor type, multivariable analysis identified other factors associated with GRFS such as patient age, performance status, and interval between diagnosis and transplantation. For patients with SAA lacking an MSD, our findings support MUDs as the preferable alternative donor option. However, selecting between an MMUD and Haplo donor remains uncertain and requires further exploration.
Asunto(s)

Texto completo: 1 Bases de datos: MEDLINE Asunto principal: Trasplante de Células Madre Hematopoyéticas / Donante no Emparentado / Enfermedad Injerto contra Huésped / Anemia Aplásica Límite: Adolescent / Adult / Child / Child, preschool / Female / Humans / Male / Middle aged Idioma: En Revista: Blood Año: 2024 Tipo del documento: Article País de afiliación: España

Texto completo: 1 Bases de datos: MEDLINE Asunto principal: Trasplante de Células Madre Hematopoyéticas / Donante no Emparentado / Enfermedad Injerto contra Huésped / Anemia Aplásica Límite: Adolescent / Adult / Child / Child, preschool / Female / Humans / Male / Middle aged Idioma: En Revista: Blood Año: 2024 Tipo del documento: Article País de afiliación: España