Second allogeneic hematopoietic stem cell transplantation in patients with inborn errors of immunity

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Alexandra Laberko
Elvira Sultanova
Aishat Idarmacheva
Yulia Skvortsova
Larisa Shelikhova
Alexei Nechesnyuk
Daria Kobyzeva
Anna Shcherbina
Michael Maschan
Alexei Maschan
Dmitry Balashov
机构
[1] Oncology and Immunology,Department of Immunology, Dmitry Rogachev National Medical Research Center of Pediatric Hematology
[2] Newcastle University,Translational and Clinical Research Institute
[3] Oncology and Immunology,Department of Hematopoietic Stem Cell Transplantation, Dmitry Rogachev National Medical Research Center of Pediatric Hematology
[4] Oncology and Immunology,Department of Radiation Therapy, Dmitry Rogachev National Medical Research Center of Pediatric Hematology
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Graft failure (GF) remains a serious issue of hematopoietic stem cell transplantation (HSCT) in inborn errors of immunity (IEI). Second HSCT is the only salvage therapy for GF. There are no uniform strategies for the second HSCTs and limited data are available on the second HSCT outcomes. 48 patients with various IEI received second allogeneic HSCT from 2013 to 2020. Different conditioning regimens were used, divided into two main groups: containing myeloablative doses of busulfan/treosulfan (n = 19) and lymphoid irradiation 2–6 Gy (n = 22). Irradiation-containing conditioning was predominantly used in suspected immune-mediated rejection of the first graft. Matched unrelated donor was used in 28 patients, mismatched related in 18, and matched related in 1. 35 patients received TCRαβ/CD19 graft depletion. The median follow-up time was 2.4 years post-HSCT. One patient died at conditioning. The OS was 0.63 (95% CI: 0.41–0.85) after busulfan/treosulfan and 0.68 (95% CI: 0.48–0.88) after irradiation-based conditioning, p = 0.66. Active infection at HSCT significantly influenced OS: 0.43 (95% CI: 0.17–0.69) versus 0.73 (95% CI: 0.58–0.88) without infection, p = 0.004. The cumulative incidence of GF was 0.15 (95% CI: 0.08–0.29). To conclude, an individualized approach is required for the second HSCT in IEI. Low-dose lymphoid irradiation in suspected immune-mediated GF may be a feasible option.
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页码:273 / 281
页数:8
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