Your browser doesn't support javascript.
loading
Allogeneic Hematopoietic Cell Transplantation in Patients Aged 50Years or Older with Severe Aplastic Anemia.
Rice, Carmel; Eikema, Dirk-Jan; Marsh, Judith C W; Knol, Cora; Hebert, Kyle; Putter, Hein; Peterson, Eefke; Deeg, H Joachim; Halkes, Stijn; Pidala, Joseph; Anderlini, Paolo; Tischer, Johanna; Kroger, Nicolaus; McDonald, Andrew; Antin, Joseph H; Schaap, Nicolaas P; Hallek, Michael; Einsele, Herman; Mathews, Vikram; Kapoor, Neena; Boelens, Jaap-Jan; Mufti, Ghulam J; Potter, Victoria; Pefault de la Tour, Régis; Eapen, Mary; Dufour, Carlo.
Afiliação
  • Rice C; Department of Haematology, King's College Hospital, London, United Kingdom.
  • Eikema DJ; EBMT Statistical Unit, Leiden, Netherlands.
  • Marsh JCW; Department of Haematology, King's College Hospital, London, United Kingdom; Department of Haematology, King's College London, London, United Kingdom. Electronic address: Judith.marsh@nhs.net.
  • Knol C; EBMT Data Office, Leiden, Netherlands.
  • Hebert K; Center for International Blood and Marrow Transplant Research, Department of Medicine, Medical College of Wisconsin, Milwaukee, Wisconsin.
  • Putter H; Department of Biomedical Data Sciences, Leiden University Medical Center, Leiden, the Netherlands.
  • Peterson E; University Medical Center Utrecht, Utrecht, Netherlands.
  • Deeg HJ; Fred Hutchinson Cancer Center, Seattle, Washinton.
  • Halkes S; Leiden University Medical Centre, Leiden, Netherlands.
  • Pidala J; H. Lee Moffitt Cancer Center, Tampa, Florida.
  • Anderlini P; MD Anderson Cancer Center, Houston, Texas.
  • Tischer J; Klinikum Grosshadern, Munich, Germany.
  • Kroger N; University Hospital Eppendorf, Hamburg, Germany.
  • McDonald A; Albert Stem Cell Transplantation Centre, Pretoria Gauteng, South Africa.
  • Antin JH; Dana Farber Cancer Institute, Boston, Massachusetts.
  • Schaap NP; Radboud University, Nijmegen Medical Centre, Netherlands.
  • Hallek M; University of Cologne, Cologne, Germany.
  • Einsele H; Universitätsklinikum Würzburg, Würzburg, Germany.
  • Mathews V; Christian Medical College Hospital, Vellore, India.
  • Kapoor N; Children's Hospital of Los Angeles, Los Angeles, California.
  • Boelens JJ; University Medical Center Utrecht, Utrecht, Netherlands.
  • Mufti GJ; Department of Haematology, King's College Hospital, London, United Kingdom; Department of Haematology, King's College London, London, United Kingdom.
  • Potter V; Department of Haematology, King's College Hospital, London, United Kingdom.
  • Pefault de la Tour R; Hopital St. Louis, Paris, France.
  • Eapen M; Center for International Blood and Marrow Transplant Research, Department of Medicine, Medical College of Wisconsin, Milwaukee, Wisconsin.
  • Dufour C; Instituto Giannina Gaslini, Genova, Italy.
Biol Blood Marrow Transplant ; 25(3): 488-495, 2019 03.
Article em En | MEDLINE | ID: mdl-30194027
We report on 499 patients with severe aplastic anemia aged ≥ 50years who underwent hematopoietic cell transplantation (HCT) from HLA-matched sibling (n = 275, 55%) or HLA-matched (8/8) unrelated donors (n = 187, 37%) between 2005 and 2016. The median age at HCT was 57.8 years; 16% of patients were 65 to 77years old. Multivariable analysis confirmed higher mortality risks for patients with performance score less than 90% (hazard ratio [HR], 1.41; 95% confidence interval [CI], 1.03 to 1.92; P = .03) and after unrelated donor transplantation (HR, 1.47; 95% CI, 1 to 2.16; P = .05). The 3-year probabilities of survival for patients with performance scores of 90 to 100 and less than 90 after HLA-matched sibling transplant were 66% (range, 57% to 75%) and 57% (range, 47% to 76%), respectively. The corresponding probabilities after HLA-matched unrelated donor transplantation were 57% (range, 48% to 67%) and 48% (range, 36% to 59%). Age at transplantation was not associated with survival, but grades II to IV acute graft-versus-host disease (GVHD) risks were higher for patients aged 65years or older (subdistribution HR [sHR], 1.7; 95% confidence interval, 1.07 to 2.72; P = .026). Chronic GVHD was lower with the GVHD prophylaxis regimens calcineurin inhibitor (CNI) + methotrexate (sHR, .52; 95% CI, .33 to .81; P = .004) and CNI alone or with other agents (sHR, .27; 95% CI, .14 to .53; P < .001) compared with CNI + mycophenolate. Although donor availability is modifiable only to a limited extent, choice of GVHD prophylaxis and selection of patients with good performance scores are key for improved outcomes.
Assuntos
Palavras-chave

Texto completo: 1 Coleções: 01-internacional Contexto em Saúde: 1_ASSA2030 / 6_ODS3_enfermedades_notrasmisibles Base de dados: MEDLINE Assunto principal: Transplante de Células-Tronco Hematopoéticas / Anemia Aplástica Tipo de estudo: Etiology_studies Limite: Aged / Female / Humans / Male / Middle aged Idioma: En Revista: Biol Blood Marrow Transplant Ano de publicação: 2019 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Contexto em Saúde: 1_ASSA2030 / 6_ODS3_enfermedades_notrasmisibles Base de dados: MEDLINE Assunto principal: Transplante de Células-Tronco Hematopoéticas / Anemia Aplástica Tipo de estudo: Etiology_studies Limite: Aged / Female / Humans / Male / Middle aged Idioma: En Revista: Biol Blood Marrow Transplant Ano de publicação: 2019 Tipo de documento: Article