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Outcomes after Haploidentical Stem Cell Transplantation with Post-Transplantation Cyclophosphamide in Patients with Primary Immunodeficiency Diseases.
Fernandes, Juliana Folloni; Nichele, Samantha; Arcuri, Leonardo Javier; Ribeiro, Lisandro; Zamperlini-Netto, Gabriele; Loth, Gisele; Rodrigues, Ana Luiza Melo; Kuwahara, Cilmara; Koliski, Adriana; Trennepohl, Joanna; Garcia, Julia Lopes; Daudt, Liane Esteves; Seber, Adriana; Gomes, Alessandra Araujo; Fasth, Anders; Pasquini, Ricardo; Hamerschlak, Nelson; Rocha, Vanderson; Bonfim, Carmem.
Afiliação
  • Fernandes JF; Hematopoietic Stem Cell Transplantation unit, Instituto de Tratamento do Câncer Infantil, Instituto da Criança, Hospital das Clínicas da Faculdade de Medicina da Universidade de São Paulo, Brazil; Hematology and Bone Marrow Transplantation Unit, Hospital Israelita Albert Einstein, São Paulo, Brazil;
  • Nichele S; Pediatric Blood and Marrow Transplantation Unit, Hospital de Clínicas da Universidade Federal do Paraná, Curitiba, Brazil; Pediatric Blood and Marrow Transplantation Unit, Hospital Nossa Senhora das Graças, Curitiba, Brazil.
  • Arcuri LJ; Hematology and Bone Marrow Transplantation Unit, Hospital Israelita Albert Einstein, São Paulo, Brazil.
  • Ribeiro L; Pediatric Blood and Marrow Transplantation Unit, Hospital de Clínicas da Universidade Federal do Paraná, Curitiba, Brazil; Pediatric Blood and Marrow Transplantation Unit, Hospital Nossa Senhora das Graças, Curitiba, Brazil.
  • Zamperlini-Netto G; Hematology and Bone Marrow Transplantation Unit, Hospital Israelita Albert Einstein, São Paulo, Brazil.
  • Loth G; Pediatric Blood and Marrow Transplantation Unit, Hospital de Clínicas da Universidade Federal do Paraná, Curitiba, Brazil; Hematopoietic Stem Cell Transplantation unit, Hospital Infantil Pequeno Príncipe, Curitiba, Brazil.
  • Rodrigues ALM; Hematopoietic Stem Cell Transplantation unit, Hospital Infantil Pequeno Príncipe, Curitiba, Brazil.
  • Kuwahara C; Hematopoietic Stem Cell Transplantation unit, Hospital Infantil Pequeno Príncipe, Curitiba, Brazil.
  • Koliski A; Pediatric Blood and Marrow Transplantation Unit, Hospital de Clínicas da Universidade Federal do Paraná, Curitiba, Brazil.
  • Trennepohl J; Pediatric Blood and Marrow Transplantation Unit, Hospital de Clínicas da Universidade Federal do Paraná, Curitiba, Brazil; Pediatric Blood and Marrow Transplantation Unit, Hospital Nossa Senhora das Graças, Curitiba, Brazil.
  • Garcia JL; Hematopoietic Stem Cell Transplantation unit, Instituto de Tratamento do Câncer Infantil, Instituto da Criança, Hospital das Clínicas da Faculdade de Medicina da Universidade de São Paulo, Brazil; Hematology and Bone Marrow Transplantation Unit, Hospital Israelita Albert Einstein, São Paulo, Brazil.
  • Daudt LE; Pediatric Blood and Marrow Transplantation Unit, Hospital de Clínicas de Porto Alegre, Universidade Federal do Rio Grande do Sul, Brazil.
  • Seber A; Pediatric Hematopoietic Cell Therapy Unit, Hospital Samaritano, São Paulo, Brazil.
  • Gomes AA; Hematopoietic Stem Cell Transplantation unit, Instituto de Tratamento do Câncer Infantil, Instituto da Criança, Hospital das Clínicas da Faculdade de Medicina da Universidade de São Paulo, Brazil; Hematopoietic Stem Cell Transplantation Unit, Hospital 9 de Julho, São Paulo, Brazil; Bone Marrow Trans
  • Fasth A; Department of Pediatrics, Sahlgrenska Academy, University of Gothenburg, Gothenburg, Sweden.
  • Pasquini R; Pediatric Blood and Marrow Transplantation Unit, Hospital de Clínicas da Universidade Federal do Paraná, Curitiba, Brazil; Pediatric Blood and Marrow Transplantation Unit, Hospital Nossa Senhora das Graças, Curitiba, Brazil.
  • Hamerschlak N; Hematology and Bone Marrow Transplantation Unit, Hospital Israelita Albert Einstein, São Paulo, Brazil.
  • Rocha V; Bone Marrow Transplantation Unit, Hospital Sírio Libanês, São Paulo, Brazil; Department of Hematology, Hospital das Clínicas da Universidade de São Paulo (LIM 31), São Paulo, Brazil.
  • Bonfim C; Pediatric Blood and Marrow Transplantation Unit, Hospital de Clínicas da Universidade Federal do Paraná, Curitiba, Brazil; Pediatric Blood and Marrow Transplantation Unit, Hospital Nossa Senhora das Graças, Curitiba, Brazil; Hematopoietic Stem Cell Transplantation unit, Hospital Infantil Pequeno Prí
Biol Blood Marrow Transplant ; 26(10): 1923-1929, 2020 10.
Article em En | MEDLINE | ID: mdl-32653621
Allogeneic hematopoietic stem cell transplantation (HCT) can cure primary immunodeficiency diseases (PID). When a HLA-matched donor is not available, a haploidentical family donor may be considered. The use of T cell-replete haploidentical HCT with post-transplantation cyclophosphamide (haplo-PTCy) in children with PID has been reported in few case series. A donor is usually readily available, and haplo-PTCy can be used in urgent cases. We studied the outcomes of 73 patients with PID who underwent haplo-PTCy, including 55 patients who did so as a first transplantation and 18 who did so as a salvage transplantation after graft failure of previous HCT. The median patient age was 1.6 years. Most of the children were male (n = 54) and had active infection at the time of transplantation (n = 50); 10 children had severe organ damage. The diagnosis was severe combined immunodeficiency (SCID) in 34 patients and non-SCID in 39 (Wiskott-Aldrich syndrome; n = 14; chronic granulomatous disease, n = 10; other PID, n = 15). The median duration of follow-up of survivors was 2 years. The cumulative incidence of neutrophil recovery was 88% in the SCID group and 84% in non-SCID group and was 81% for first transplantations and 83% after a salvage graft. At 100 days, the cumulative incidence of acute GVHD grade II-IV and III-IV was 33% and 14%, respectively. The majority of patients reached 200/µL CD4+ and 1000/µL CD3+ cell counts between 3 and 6 months. The estimated 2-year overall survival was 66%; it was 64% for SCID patients and 65% for non-SCID patients and 63% for first HCT and 77% for salvage transplantations. Twenty-five patients died, most of them due to infection early after transplantation (before 100 days). In conclusion, haplo-PTCy is a feasible procedure, can cure two-thirds of children with PID, and can be used as rescue treatment for previous graft failure. © 2020 American Society for Transplantation and Cellular Therapy. Published by Elsevier Inc.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Transplante de Células-Tronco Hematopoéticas / Doenças da Imunodeficiência Primária / Doença Enxerto-Hospedeiro Limite: Child / Female / Humans / Infant / Male Idioma: En Ano de publicação: 2020 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Transplante de Células-Tronco Hematopoéticas / Doenças da Imunodeficiência Primária / Doença Enxerto-Hospedeiro Limite: Child / Female / Humans / Infant / Male Idioma: En Ano de publicação: 2020 Tipo de documento: Article