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Hematopoietic stem cell transplantation for adolescents and adults with inborn errors of immunity: an EBMT IEWP study.
Albert, Michael H; Sirait, Tiarlan; Eikema, Dirk-Jan; Bakunina, Katerina; Wehr, Claudia; Suarez, Felipe; Fox, Maria Laura; Mahlaoui, Nizar; Gennery, Andrew R; Lankester, Arjan C; Beier, Rita; Bernardo, Maria Ester; Bigley, Venetia; Lindemans, Caroline A; Burns, Siobhan O; Carpenter, Ben; Dybko, Jaroslaw; Güngör, Tayfun; Hauck, Fabian; Lum, Su Han; Balashov, Dmitry; Meisel, Roland; Moshous, Despina; Schulz, Ansgar; Speckmann, Carsten; Slatter, Mary A; Strahm, Brigitte; Uckan-Cetinkaya, Duygu; Meyts, Isabelle; Vallée, Tanja C; Wynn, Robert; Neven, Bénédicte; Morris, Emma C; Aiuti, Alessandro; Maschan, Alexei; Aljurf, Mahmoud; Gedde-Dahl, Tobias; Gurman, Gunhan; Bordon, Victoria; Kriván, Gergely; Locatelli, Franco; Porta, Fulvio; Valcárcel, David; Beguin, Yves; Faraci, Maura; Kröger, Nicolaus; Kulagin, Aleksandr; Shaw, Peter J; Veelken, Joan Hendrik; Diaz de Heredia, Cristina.
Afiliação
  • Albert MH; Department of Pediatrics, Dr. von Hauner Children's Hospital, University Hospital, Ludwig-Maximilians-Universität, Munich, Germany.
  • Sirait T; Statistical Unit and Data Office, European Society for Blood and Marrow Transplantation (EBMT), Leiden, The Netherlands.
  • Eikema DJ; Statistical Unit and Data Office, European Society for Blood and Marrow Transplantation (EBMT), Leiden, The Netherlands.
  • Bakunina K; Statistical Unit and Data Office, European Society for Blood and Marrow Transplantation (EBMT), Leiden, The Netherlands.
  • Wehr C; Institute for Immunodeficiency, Center for Chronic Immunodeficiency, Faculty of Medicine, University of Freiburg, Freiburg, Germany.
  • Suarez F; Department of Medicine I, Medical Center - University of Freiburg, Faculty of Medicine, University of Freiburg, Freiburg, Germany.
  • Fox ML; Department of Adult Hematology, Necker-Enfants Malades University Hospital, Assistance Publique-Hôpitaux de Paris (AP-HP), Paris, France.
  • Mahlaoui N; Department of Hematology, Hospital Universitari Vall d'Hebron, Experimental Hematology, Vall d'Hebron Institute of Oncology (VHIO), Vall d'Hebron Hospital Campus, Barcelona, Spain.
  • Gennery AR; Pediatric Immuno-Hematology and Rheumatology Unit, Necker-Enfants University Hospital and French National Reference Center for Primary Immunodeficiencies (CEREDIH), AP-HP, Paris, France.
  • Lankester AC; Department of Pediatric Immunology & Haematopoietic Stem Cell Transplantation (HSCT), Great North Children's Hospital, Newcastle upon Tyne, United Kingdom.
  • Beier R; Translational and Clinical Research Institute, Newcastle University, Newcastle upon Tyne, United Kingdom.
  • Bernardo ME; Department of Pediatrics, Pediatric Stem Cell Transplantation Program, Willem-Alexander Children's Hospital, Leiden University Medical Center, Leiden, The Netherlands.
  • Bigley V; Department of Pediatric Hematology and Oncology, Medizinische Hochschule Hannover (MHH), Hannover, Germany.
  • Lindemans CA; Department of Pediatric Immunohematology, Istituto Di Ricovero e Cura a Carattere Scientifico (IRCCS) Ospedale San Raffaele, Milan, Italy.
  • Burns SO; Translational and Clinical Research Institute, Newcastle University, Newcastle upon Tyne, United Kingdom.
  • Carpenter B; Northern Center for Cancer Care, Newcastle upon Tyne Hospitals National Health Service (NHS) Foundation Trust, Newcastle upon Tyne, United Kingdom.
  • Dybko J; Department of Pediatric Immunology, University Medical Center Utrecht, Utrecht, The Netherlands.
  • Güngör T; Department of Pediatric Blood and Bone Marrow Transplantation, Princess Maxima Center, Utrecht, The Netherlands.
  • Hauck F; Department of Immunology, Royal Free London Hospitals NHS Foundation Trust, London, United Kingdom.
  • Lum SH; Institute of Immunity and Transplantation, University College London (UCL), London, United Kingdom.
  • Balashov D; Department of Clinical Hematology, University College London Hospitals NHS Foundation Trust, London, United Kingdom.
  • Meisel R; Department of Hematology and Cellular Transplantation, Lower Silesian Center of Oncology, Wroclaw, Poland.
  • Moshous D; Department of Hematology/Oncology/Immunology, Gene-Therapy, and Stem Cell Transplantation, University Children's Hospital Zurich - Eleonore Foundation & Children's Research Center (CRC), Zürich, Switzerland.
  • Schulz A; Department of Pediatrics, Dr. von Hauner Children's Hospital, University Hospital, Ludwig-Maximilians-Universität, Munich, Germany.
  • Speckmann C; Department of Pediatric Immunology & Haematopoietic Stem Cell Transplantation (HSCT), Great North Children's Hospital, Newcastle upon Tyne, United Kingdom.
  • Slatter MA; Department of Hematopoietic Stem Cell Transplantation, Dmitriy Rogachev National Center for Pediatric Hematology, Oncology, and Immunology, Moscow, Russian Federation.
  • Strahm B; Division of Pediatric Stem Cell Therapy, Department of Paediatric Oncology, Hematology and Clinical Immunology, Medical Faculty, Heinrich-Heine-University, Düsseldorf, Germany.
  • Uckan-Cetinkaya D; Department of Pediatric Immunology, Hematology, and Rheumatology, Necker-Enfants Malades University Hospital, AP-HP, Paris, France.
  • Meyts I; Department of Pediatrics, University Medical Center Ulm, Ulm, Germany.
  • Vallée TC; Institute for Immunodeficiency, Center for Chronic Immunodeficiency, Faculty of Medicine, University of Freiburg, Freiburg, Germany.
  • Wynn R; Department of Pediatric Hematology and Oncology, Center for Pediatrics and Adolescent Medicine, Faculty of Medicine, University of Freiburg, Freiburg, Germany.
  • Neven B; Department of Pediatric Immunology & Haematopoietic Stem Cell Transplantation (HSCT), Great North Children's Hospital, Newcastle upon Tyne, United Kingdom.
  • Morris EC; Translational and Clinical Research Institute, Newcastle University, Newcastle upon Tyne, United Kingdom.
  • Aiuti A; Department of Pediatric Hematology and Oncology, Center for Pediatrics and Adolescent Medicine, Faculty of Medicine, University of Freiburg, Freiburg, Germany.
  • Maschan A; Department of Pediatrics, Bone Marrow Transplantation (BMT) Unit, Hacettepe University, Faculty of Medicine, Ankara, Turkey.
  • Aljurf M; Department of Pediatrics, University Hospitals Leuven, Leuven, Belgium.
  • Gedde-Dahl T; Department of Microbiology, Immunology, and Transplantation, Katholieke Universiteit (KU) Leuven, Leuven, Belgium.
  • Gurman G; Department of Pediatrics, Dr. von Hauner Children's Hospital, University Hospital, Ludwig-Maximilians-Universität, Munich, Germany.
  • Bordon V; Blood and Marrow Transplant Program, Royal Manchester Children's Hospital, Manchester, United Kingdom.
  • Kriván G; Department of Pediatric Immunology, Hematology, and Rheumatology, Necker-Enfants Malades University Hospital, AP-HP, Paris, France.
  • Locatelli F; Department of Immunology, Royal Free London Hospitals NHS Foundation Trust, London, United Kingdom.
  • Porta F; Institute of Immunity and Transplantation, University College London (UCL), London, United Kingdom.
  • Valcárcel D; Department of Clinical Hematology, University College London Hospitals NHS Foundation Trust, London, United Kingdom.
Blood ; 140(14): 1635-1649, 2022 10 06.
Article em En | MEDLINE | ID: mdl-35344580
ABSTRACT
Allogeneic hematopoietic stem cell transplantation (HSCT) is the gold standard curative therapy for infants and children with many inborn errors of immunity (IEI), but adolescents and adults with IEI are rarely referred for transplant. Lack of published HSCT outcome data outside small, single-center studies and perceived high risk of transplant-related mortality have delayed the adoption of HSCT for IEI patients presenting or developing significant organ damage later in life. This large retrospective, multicenter HSCT outcome study reports on 329 IEI patients (age range, 15-62.5 years at HSCT). Patients underwent first HSCT between 2000 and 2019. Primary endpoints were overall survival (OS) and event-free survival (EFS). We also evaluated the influence of IEI-subgroup and IEI-specific risk factors at HSCT, including infections, bronchiectasis, colitis, malignancy, inflammatory lung disease, splenectomy, hepatic dysfunction, and systemic immunosuppression. At a median follow-up of 44.3 months, the estimated OS at 1 and 5 years post-HSCT for all patients was 78% and 71%, and EFS was 65% and 62%, respectively, with low rates of severe acute (8%) or extensive chronic (7%) graft-versus-host disease. On univariate analysis, OS and EFS were inferior in patients with primary antibody deficiency, bronchiectasis, prior splenectomy, hepatic comorbidity, and higher hematopoietic cell transplant comorbidity index scores. On multivariable analysis, EFS was inferior in those with a higher number of IEI-associated complications. Neither age nor donor had a significant effect on OS or EFS. We have identified age-independent risk factors for adverse outcome, providing much needed evidence to identify which patients are most likely to benefit from HSCT.
Assuntos

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Bronquiectasia / Transplante de Células-Tronco Hematopoéticas / Doença Enxerto-Hospedeiro Idioma: En Ano de publicação: 2022 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Bronquiectasia / Transplante de Células-Tronco Hematopoéticas / Doença Enxerto-Hospedeiro Idioma: En Ano de publicação: 2022 Tipo de documento: Article