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Solid organ transplantation after hematopoietic stem cell transplantation in childhood: A multicentric retrospective survey.
Faraci, Maura; Bertaina, Alice; Dalissier, Arnaud; Ifversen, Marianne; Schulz, Ansgar; Gennery, Andrew; Burkhardt, Birgit; Badell Serra, Isabel; Diaz-de-Heredia, Cristina; Lanino, Edoardo; Lankester, Arjan C; Gruhn, Bernd; Matthes-Martin, Susanne; Kühl, Joern S; Varotto, Stefania; Paillard, Catherine; Guilmatre, Audrey; Sastre, Ana; Abecasis, Manuel; Garwer, Birgit; Sedlacek, Petr; Boelens, Jaap J; Beohou, Eric; Bader, Peter.
Afiliação
  • Faraci M; Hematopoietic Stem Cell Transplantation Unit, Hematology-Oncology, Istituto G Gaslini, Genova, Italy.
  • Bertaina A; Dipartimento di Onco-Ematologia Pediatrica, IRCSS Ospedale Pediatrico Bambino Gesù, Rome, Italy.
  • Dalissier A; Division of Stem Cell Transplantation and Regenerative Medicine, Department of Pediatrics, School of Medicine, Stanford University, Stanford, California.
  • Ifversen M; European Society for Blood and Marrow Transplantation Pediatric Disease Working Party, Paris, France.
  • Schulz A; Department for Children and Adolescents, Rigshospitalet, Copenhagen University Hospital, Copenhagen, Denmark.
  • Gennery A; Department of Pediatrics, University Medical Center, Ulm, Germany.
  • Burkhardt B; Institute of Cellular Medicine, Pediatric Immunology Department, Newcastle University, Great North Children's Hospital, Newcastle-upon-Tyne, UK.
  • Badell Serra I; Pediatric Hematology and Oncology, University Hospital Münster, Muenster, Germany.
  • Diaz-de-Heredia C; Pediatric Hematopoietic Transplant Unit, Sant Pau Hospital, Barcelona, Spain.
  • Lanino E; Department of Pediatric Oncology and Hematology, Hospital Universitario Vall d'Hebron, Barcelona, Spain.
  • Lankester AC; Hematopoietic Stem Cell Transplantation Unit, Hematology-Oncology, Istituto G Gaslini, Genova, Italy.
  • Gruhn B; Department of Pediatrics Stem Cell Transplantation Program, Leiden University Medical Center, Leiden, The Netherlands.
  • Matthes-Martin S; Department of Pediatrics, Jena University Hospital, Jena, Germany.
  • Kühl JS; St Anna Children's Hospital, Medical University of Vienna, Vienna, Austria.
  • Varotto S; Department Pediatric Hematology, Oncology, Hemostaseology, Universitätsklinikum Leipzig, Leipzig, Germany.
  • Paillard C; Clinic of Pediatric Hemato-Oncology, Department of Women's and Children's Health, University Hospital of Padova, Padova, Italy.
  • Guilmatre A; Hematology, Oncology and Stem Cell Transplantation, Department of Pediatrics, Hôpital Hautepierre, Strasbourg, France.
  • Sastre A; Service of Pediatric Hematology-Oncology, Hôpital Armand Trousseau, Paris, France.
  • Abecasis M; Unidad de Hematología y Oncología Pediátrica, Hospital Universitario La Paz, Madrid, Spain.
  • Garwer B; Instute Portugues Oncologia Lisboa, Lisboa, Portugal.
  • Sedlacek P; University Hospital Eppendorf, Hamburg, Germany.
  • Boelens JJ; University Hospital Motol, Prague, Czech Republic.
  • Beohou E; Pediatric Blood and Marrow Transplantation Program, Laboratory for Translational Immunology Tumor-immunology, University Medical Center, Utrecht, The Netherlands.
  • Bader P; Stem Cell Transplant and Cellular Therapies Pediatrics, Memorial Sloan Kettering Cancer Center, New York, New York.
Am J Transplant ; 19(6): 1798-1805, 2019 06.
Article em En | MEDLINE | ID: mdl-30586230
We report data obtained from a retrospective multicenter pediatric survey on behalf of the European Society for Blood and Marrow Transplantation (EBMT). Information on solid organ transplantation (SOT) performed in pediatric recipients of either autologous or allogeneic hematopoietic stem cell transplantation (HSCT) between 1984 and 2016 was collected in 20 pediatric EBMT Centers (25.6%). Overall, we evaluated data on 44 SOTs following HSCT including 20 liver (LTx), 12 lung (LuTx), 6 heart (HTx), and 6 kidney (KTx) transplantations. The indication for SOT was organ failure related to intractable graft-vs-host disease in 16 children (36.3%), acute or chronic HSCT-related toxicity in 18 (40.9%), and organ dysfunction related to the underlying disease in 10 (22.8%). The median follow-up was 10.9 years (95% confidence interval: 1.7-29.5). The overall survival rate at 1 and 5 years after SOT was 85.7% and 80.4%, respectively: it was 74% and 63.2% after LTx, 83.2% after HTx, and 100% equally after LuTx and KTx. This multicenter survey confirms that SOT represents a promising option in children with severe organ failure occurring after HSCT. Additional studies are needed to further establish the effectiveness of SOT after HSCT and to better understand the mechanism underlying this encouraging success.
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Texto completo: 1 Bases de dados: MEDLINE Assunto principal: Transplante de Órgãos / Transplante de Células-Tronco Hematopoéticas / Doença Enxerto-Hospedeiro Tipo de estudo: Etiology_studies / Incidence_studies / Observational_studies / Prognostic_studies / Risk_factors_studies Limite: Adolescent / Child / Child, preschool / Female / Humans / Infant / Male País/Região como assunto: Europa Idioma: En Revista: Am J Transplant Assunto da revista: TRANSPLANTE Ano de publicação: 2019 Tipo de documento: Article País de afiliação: Itália

Texto completo: 1 Bases de dados: MEDLINE Assunto principal: Transplante de Órgãos / Transplante de Células-Tronco Hematopoéticas / Doença Enxerto-Hospedeiro Tipo de estudo: Etiology_studies / Incidence_studies / Observational_studies / Prognostic_studies / Risk_factors_studies Limite: Adolescent / Child / Child, preschool / Female / Humans / Infant / Male País/Região como assunto: Europa Idioma: En Revista: Am J Transplant Assunto da revista: TRANSPLANTE Ano de publicação: 2019 Tipo de documento: Article País de afiliação: Itália