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Published in: Journal of Clinical Immunology 8/2023

16-07-2023 | Graft-Versus-Host Disease | Original Article

An International Survey of Allogeneic Hematopoietic Cell Transplantation for X-Linked Agammaglobulinemia

Authors: Akira Nishimura, Ramya Uppuluri, Revathi Raj, Venkateswaran Vellaichamy Swaminathan, Yifei Cheng, Rolla F. Abu-Arja, Bin Fu, Alexandra Laberko, Michael H. Albert, Fabian Hauck, Giorgia Bucciol, Venetia Bigley, Suzanne Elcombe, Gaurav Kharya, Cornelis Jan H Pronk, Claudia Wehr, Bénédicte Neven, Klaus Warnatz, Isabelle Meyts, Tomohiro Morio, Andrew R. Gennery, Hirokazu Kanegane

Published in: Journal of Clinical Immunology | Issue 8/2023

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Abstract

Purpose

X-linked agammaglobulinemia (XLA) is an inborn error of immunity caused by variants in Bruton’s tyrosine kinase (BTK). XLA patients require lifelong immunoglobulin replacement therapy (IgRT). Only few XLA patients are indicated for allogeneic hematopoietic cell transplantation (HCT) because of severe complications. Accordingly, the published transplantation experience in XLA is minimal. We aimed to collect clinical data of XLA patients who received HCT in an international framework and to establish appropriate transplantation criteria and methods for XLA patients.

Methods

XLA patients were recruited through a questionnaire and a literature review. The data are on patient characteristics and transplantation methods and outcomes.

Results

In this study, twenty-two XLA patients who underwent HCT were recruited. The indication for HCT was recurrent or life-threatening infection in sixteen patients, malignancy in three, and other factors in three. A myeloablative conditioning, reduced toxicity myeloablative conditioning (RT-MAC), and reduced intensity conditioning (RIC) were selected in four, ten, and eight patients, respectively. Engraftment was achieved in 21 patients (95%). In all patients, 2-year overall survival (OS) and event-free survival (EFS) were 86% and 77%, respectively. In patients who received RT-MAC or RIC using treosulfan, busulfan, or melphalan, 2-year OS and EFS were 82% and 71%, respectively. Finally, twenty-one patients (95%) obtained complete or stable high-level mixed chimerism (50–95%), and the 1-year discontinuation rate of IgRT was 89%.

Conclusion

Based on the concept in which IgRT is the standard treatment for XLA, HCT may be an effective and safe alternative treatment option for XLA patients, and IgRT can be discontinued following transplantation. It is ideal to perform HCT in XLA patients for whom transplantation is indicated before they develop organ damage.
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Metadata
Title
An International Survey of Allogeneic Hematopoietic Cell Transplantation for X-Linked Agammaglobulinemia
Authors
Akira Nishimura
Ramya Uppuluri
Revathi Raj
Venkateswaran Vellaichamy Swaminathan
Yifei Cheng
Rolla F. Abu-Arja
Bin Fu
Alexandra Laberko
Michael H. Albert
Fabian Hauck
Giorgia Bucciol
Venetia Bigley
Suzanne Elcombe
Gaurav Kharya
Cornelis Jan H Pronk
Claudia Wehr
Bénédicte Neven
Klaus Warnatz
Isabelle Meyts
Tomohiro Morio
Andrew R. Gennery
Hirokazu Kanegane
Publication date
16-07-2023
Publisher
Springer US
Published in
Journal of Clinical Immunology / Issue 8/2023
Print ISSN: 0271-9142
Electronic ISSN: 1573-2592
DOI
https://doi.org/10.1007/s10875-023-01551-2

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