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Long-Term Outcomes of Cord Blood Transplantation from an HLA-Identical Sibling for Patients with Bone Marrow Failure Syndromes: A Report From Eurocord, Cord Blood Committee and Severe Aplastic Anemia Working Party of the European Society for Blood and Marrow Transplantation.
Pagliuca, Simona; Peffault de Latour, Régis; Volt, Fernanda; Locatelli, Franco; Zecca, Marco; Dalle, Jean-Hugues; Comoli, Patrizia; Vettenranta, Kim; Diaz, Miguel Angel; Reuven, Or; Bertrand, Yves; Diaz de Heredia, Cristina; Nagler, Arnon; Ghavamzadeh, Ardeshir; Sufliarska, Sabina; Lawson, Sarah; Kenzey, Chantal; Rocha, Vanderson; Dufour, Carlo; Gluckman, Eliane; Passweg, Jakob; Ruggeri, Annalisa.
Afiliação
  • Pagliuca S; Hôpital Saint-Louis-Assistance Publique-Hôpitaux de Paris, Paris, France.
  • Peffault de Latour R; Hôpital Saint-Louis-Assistance Publique-Hôpitaux de Paris, Paris, France.
  • Volt F; Eurocord, Hôpital Saint Louis, Paris, France; Monacord, Monacord, Centre Scientifique de Monaco, Monaco.
  • Locatelli F; Oncoematologia Pediatrica e Medicina Trasfusionale IRCCS Ospedale Pediatrico Bambino Gesù, Università di Pavia, Rome, Italy.
  • Zecca M; Oncoematologia Pediatrica and Cell Factory, Fondazione IRCCS Policlinico S. Matteo, Pavia, Italy.
  • Dalle JH; Pediatric Haematology Immunology, Robert Debre Hospital, Paris, France and Paris Diderot University, Paris, France.
  • Comoli P; Oncoematologia Pediatrica and Cell Factory, Fondazione IRCCS Policlinico S. Matteo, Pavia, Italy.
  • Vettenranta K; University of Helsinki Children's Hospital, Helsinki, Finland.
  • Diaz MA; Niño Jesus Children's Hospital, Madrid, Spain.
  • Reuven O; Department of Bone Marrow Transplantation, Hadassah Hebrew University Medical Center, Jerusalem, Israel.
  • Bertrand Y; Institut d'Hématologie et Oncologie Pédiatrique, CHU Lyon, Lyon, France.
  • Diaz de Heredia C; Servicio de Hematologia y Oncologia Pediátrica, Hospital Universitario Vall d'Hebron, Barcelona, Spain.
  • Nagler A; Hematology Division, Chaim Sheba Medical Center and Tel Aviv University, Tel-Hashomer, Ramat-Gan, Israel.
  • Ghavamzadeh A; Hematology-Oncology and Stem Cell Transplantation Research Center, Tehran University of Medical Sciences, Tehran, Iran.
  • Sufliarska S; Bone Marrow Transplantation Unit, Comenius University Children's Hospital, Bratislava, Slovakia.
  • Lawson S; Department of Haematology, Birmingham Children's Hospital, Birmingham, United Kingdom.
  • Kenzey C; Eurocord, Hôpital Saint Louis, Paris, France; Monacord, Monacord, Centre Scientifique de Monaco, Monaco.
  • Rocha V; Eurocord, Hôpital Saint Louis, Paris, France; Churchill Hospital, Oxford University, Oxford, United Kingdom.
  • Dufour C; Hematology Unit, Giannina Gaslini Children's Hospital, Genoa, Italy.
  • Gluckman E; Eurocord, Hôpital Saint Louis, Paris, France; Monacord, Monacord, Centre Scientifique de Monaco, Monaco.
  • Passweg J; Klinik für Hämatologie Bereich Innere Medizin Universitätsspital Basel, Basel, Switzerland.
  • Ruggeri A; Eurocord, Hôpital Saint Louis, Paris, France; Monacord, Monacord, Centre Scientifique de Monaco, Monaco; Service d'Hématologie et Thérapie Cellulaire, Hôpital Saint-Antoine, Paris, France. Electronic address: annalisa.ruggeri@aphp.fr.
Biol Blood Marrow Transplant ; 23(11): 1939-1948, 2017 Nov.
Article em En | MEDLINE | ID: mdl-28797779
ABSTRACT
Cord blood transplantation (CBT) from HLA-identical siblings is an attractive option for patients with bone marrow failure (BMF) syndrome because of the low risk of graft-versus-host disease (GVHD) and the absence of risk to the donor. We analyzed outcomes of 117 patients with inherited or acquired BMF syndrome who received CBT from a related HLA-identical donor in European Society for Blood and Marrow Transplantation centers between 1988 and 2014. Ninety-seven patients had inherited and 20 patients acquired BMF syndrome. Eighty-two patients received a single cord blood (CB) unit, whereas 35 patients received a combination of CB and bone marrow cells from the same donor. Median age at CBT was 6.7 years, and median follow-up was 86.7 months. The cumulative incidence function (CIF) of neutrophil recovery was 88.8% (95% CI, 83.1% to 94.9%), 100-day CIF of grades II to IV acute GVHD was 15.2%, and 7-year CIF of chronic GVHD was 14.5%. Overall survival at 7 years was 87.9% (95% CI, 80.8% to 92.6%), 89% for inherited and 81% for acquired BMF syndromes (P = .66). Results of this study are consistent with outcomes of bone marrow transplantation shown by previous series in the same setting and indicate that in pediatric patients with BMF syndrome, CBT from an HLA-identical sibling donor is associated with excellent long-term outcomes and that collection of CB unit at birth of a new sibling is strongly recommended.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Doenças da Medula Óssea / Transplante de Células-Tronco de Sangue do Cordão Umbilical / Hemoglobinúria Paroxística / Antígenos HLA / Anemia Aplástica Limite: Adolescent / Child / Child, preschool / Female / Humans / Infant / Male País como assunto: Europa Idioma: En Ano de publicação: 2017 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Doenças da Medula Óssea / Transplante de Células-Tronco de Sangue do Cordão Umbilical / Hemoglobinúria Paroxística / Antígenos HLA / Anemia Aplástica Limite: Adolescent / Child / Child, preschool / Female / Humans / Infant / Male País como assunto: Europa Idioma: En Ano de publicação: 2017 Tipo de documento: Article