Hematopoietic stem cell transplantation for adolescents and adults with inborn errors of immunity: an EBMT IEWP study

Author:

Albert Michael H.1ORCID,Sirait Tiarlan2,Eikema Dirk-Jan2,Bakunina Katerina2,Wehr Claudia34,Suarez Felipe5,Fox Maria Laura6ORCID,Mahlaoui Nizar7ORCID,Gennery Andrew R.89,Lankester Arjan C.10,Beier Rita11,Bernardo Maria Ester12,Bigley Venetia913ORCID,Lindemans Caroline A.1415,Burns Siobhan O.1617,Carpenter Ben18ORCID,Dybko Jaroslaw19,Güngör Tayfun20ORCID,Hauck Fabian1ORCID,Lum Su Han8,Balashov Dmitry21,Meisel Roland22ORCID,Moshous Despina23,Schulz Ansgar24,Speckmann Carsten325,Slatter Mary A.89,Strahm Brigitte25ORCID,Uckan-Cetinkaya Duygu26,Meyts Isabelle2728ORCID,Vallée Tanja C.1,Wynn Robert29,Neven Bénédicte23,Morris Emma C.161718,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,Fagioli Franca,Felber Matthias,Gruhn Bernd,Holter Wolfgang,Rössig Claudia,Sedlacek Petr,Apperley Jane,Ayas Mouhab,Bodova Ivana,Choi Goda,Cornelissen J.J.,Sirvent Anne,Khan Anjum,Kupesiz Alphan,Lenhoff Stig,Ozdogu Hakan,von der Weid Nicolas,Rovira Montserrat,Schots Rik,Vinh Donald C.

Affiliation:

1. 1Department of Pediatrics, Dr. von Hauner Children’s Hospital, University Hospital, Ludwig-Maximilians-Universität, Munich, Germany

2. 2Statistical Unit and Data Office, European Society for Blood and Marrow Transplantation (EBMT), Leiden, The Netherlands

3. 3Institute for Immunodeficiency, Center for Chronic Immunodeficiency, Faculty of Medicine, University of Freiburg, Freiburg, Germany

4. 4Department of Medicine I, Medical Center - University of Freiburg, Faculty of Medicine, University of Freiburg, Freiburg, Germany

5. 5Department of Adult Hematology, Necker-Enfants Malades University Hospital, Assistance Publique-Hôpitaux de Paris (AP-HP), Paris, France

6. 6Department of Hematology, Hospital Universitari Vall d’Hebron, Experimental Hematology, Vall d’Hebron Institute of Oncology (VHIO), Vall d’Hebron Hospital Campus, Barcelona, Spain

7. 7Pediatric Immuno-Hematology and Rheumatology Unit, Necker-Enfants University Hospital and French National Reference Center for Primary Immunodeficiencies (CEREDIH), AP-HP, Paris, France

8. 8Department of Pediatric Immunology & Haematopoietic Stem Cell Transplantation (HSCT), Great North Children’s Hospital, Newcastle upon Tyne, United Kingdom

9. 9Translational and Clinical Research Institute, Newcastle University, Newcastle upon Tyne, United Kingdom

10. 10Department of Pediatrics, Pediatric Stem Cell Transplantation Program, Willem-Alexander Children’s Hospital, Leiden University Medical Center, Leiden, The Netherlands

11. 11Department of Pediatric Hematology and Oncology, Medizinische Hochschule Hannover (MHH), Hannover, Germany

12. 12Department of Pediatric Immunohematology, Istituto Di Ricovero e Cura a Carattere Scientifico (IRCCS) Ospedale San Raffaele, Milan, Italy

13. 13Northern Center for Cancer Care, Newcastle upon Tyne Hospitals National Health Service (NHS) Foundation Trust, Newcastle upon Tyne, United Kingdom

14. 14Department of Pediatric Immunology, University Medical Center Utrecht, Utrecht, The Netherlands

15. 15Department of Pediatric Blood and Bone Marrow Transplantation, Princess Maxima Center, Utrecht, The Netherlands

16. 16Department of Immunology, Royal Free London Hospitals NHS Foundation Trust, London, United Kingdom

17. 17Institute of Immunity and Transplantation, University College London (UCL), London, United Kingdom

18. 18Department of Clinical Hematology, University College London Hospitals NHS Foundation Trust, London, United Kingdom

19. 19Department of Hematology and Cellular Transplantation, Lower Silesian Center of Oncology, Wroclaw, Poland

20. 20Department of Hematology/Oncology/Immunology, Gene-Therapy, and Stem Cell Transplantation, University Children's Hospital Zurich – Eleonore Foundation & Children's Research Center (CRC), Zürich, Switzerland

21. 21Department of Hematopoietic Stem Cell Transplantation, Dmitriy Rogachev National Center for Pediatric Hematology, Oncology, and Immunology, Moscow, Russian Federation

22. 22Division of Pediatric Stem Cell Therapy, Department of Paediatric Oncology, Hematology and Clinical Immunology, Medical Faculty, Heinrich-Heine-University, Düsseldorf, Germany

23. 23Department of Pediatric Immunology, Hematology, and Rheumatology, Necker-Enfants Malades University Hospital, AP-HP, Paris, France

24. 24Department of Pediatrics, University Medical Center Ulm, Ulm, Germany

25. 25Department of Pediatric Hematology and Oncology, Center for Pediatrics and Adolescent Medicine, Faculty of Medicine, University of Freiburg, Freiburg, Germany

26. 26Department of Pediatrics, Bone Marrow Transplantation (BMT) Unit, Hacettepe University, Faculty of Medicine, Ankara, Turkey

27. 27Department of Pediatrics, University Hospitals Leuven, Leuven, Belgium

28. 28Department of Microbiology, Immunology, and Transplantation, Katholieke Universiteit (KU) Leuven, Leuven, Belgium

29. 29Blood and Marrow Transplant Program, Royal Manchester Children’s Hospital, Manchester, United Kingdom

Abstract

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.

Publisher

American Society of Hematology

Subject

Cell Biology,Hematology,Immunology,Biochemistry

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