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

Authors :
Michael H. Albert
Tiarlan Sirait
Dirk-Jan Eikema
Katerina Bakunina
Claudia Wehr
Felipe Suarez
Maria Laura Fox
Nizar Mahlaoui
Andrew R. Gennery
Arjan C. Lankester
Rita Beier
Maria Ester Bernardo
Venetia Bigley
Caroline A. Lindemans
Siobhan O. Burns
Ben Carpenter
Jaroslaw Dybko
Tayfun Güngör
Fabian Hauck
Su Han Lum
Dmitry Balashov
Roland Meisel
Despina Moshous
Ansgar Schulz
Carsten Speckmann
Mary A. Slatter
Brigitte Strahm
Duygu Uckan-Cetinkaya
Isabelle Meyts
Tanja C. Vallée
Robert Wynn
Bénédicte Neven
Emma C. Morris
Alessandro Aiuti
Alexei Maschan
Mahmoud Aljurf
Tobias Gedde-Dahl
Gunhan Gurman
Victoria Bordon
Gergely Kriván
Franco Locatelli
Fulvio Porta
David Valcárcel
Yves Beguin
Maura Faraci
Nicolaus Kröger
Aleksandr Kulagin
Peter J. Shaw
Joan Hendrik Veelken
Cristina Diaz de Heredia
Franca Fagioli
Matthias Felber
Bernd Gruhn
Wolfgang Holter
Claudia Rössig
Petr Sedlacek
Jane Apperley
Mouhab Ayas
Ivana Bodova
Goda Choi
J.J. Cornelissen
Anne Sirvent
Anjum Khan
Alphan Kupesiz
Stig Lenhoff
Hakan Ozdogu
Nicolas von der Weid
Montserrat Rovira
Rik Schots
Donald C. Vinh
Clinical sciences
Hematology
Source :
Blood. 140:1635-1649
Publication Year :
2022
Publisher :
American Society of Hematology, 2022.

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. ispartof: BLOOD vol:140 issue:14 pages:1635-1649 ispartof: location:United States status: published

Details

ISSN :
15280020, 00064971, and 16351649
Volume :
140
Database :
OpenAIRE
Journal :
Blood
Accession number :
edsair.doi.dedup.....8134ee0ffbc2da88fe54670c0b6c8bbe