Variables affecting outcomes after allogeneic hematopoietic stem cell transplant for cerebral adrenoleukodystrophy.

Robert Chiesa, Jaap Jan Boelens, Christine N Duncan, Jörn-Sven Kühl, Caroline Sevin, Neena Kapoor, Vinod K Prasad, Caroline A Lindemans, Simon A Jones, Hernan M Amartino, Mattia Algeri, Nancy Bunin, Cristina Diaz-de-Heredia, Daniel J Loes, Esther Shamir, Alison Timm, Elizabeth McNeil, Andrew C Dietz, Paul J Orchard

Journal: Blood advances 2022;6(5):1512-1524

PMID: 34781360

Abstract

Allogeneic hematopoietic stem cell transplantation (allo-HSCT) in early cerebral adrenoleukodystrophy can stabilize neurologic function and improve survival but has associated risks including transplant-related mortality (TRM), graft failure, and graft-versus-host disease (GVHD). An observational study of 59 patients with median age at allo-HSCT of 8 years addressed impact of donor source, donor match, conditioning regimen, and cerebral disease stage on first allo-HSCT outcomes. Efficacy analyses included 53 patients stratified by disease category: advanced disease (AD; n = 16) with Loes score >9 or neurological function score (NFS) >1 and 2 early disease (ED) cohorts (ED1 [Loes ≤4 and NFS ≤1; n = 24] and ED2 [Loes >4-9 and NFS ≤1; n = 13]). Survival free of major functional disabilities and without second allo-HSCT at 4 years was significantly higher in the ED (66%) vs AD (41%) cohort (P = .015) and comparable between ED1 and ED2 cohorts (P = .991). The stabilization of neurologic function posttransplant was greater in the ED vs AD cohort, with a median change from baseline at 24 months after allo-HSCT in NFS and Loes score, respectively, of 0 and 0.5 in ED1 (n = 13), 0.5 and 0 in ED2 (n = 6), and 2.5 and 3.0 (n = 4) in AD cohort. TRM was lower in the ED (7%) compared with the AD (22%) cohort; however, the difference was not significant (P = .094). Transplant-related safety outcomes were also affected by transplant-related characteristics: graft failure incidence was significantly higher with unrelated umbilical cord grafts vs matched related donors (P = .039), and acute GVHD and graft failure incidences varied by conditioning regimen. This study was registered at www://clinicaltrials.gov as #NCT02204904.

© 2022 by The American Society of Hematology. Licensed under Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International (CC BY-NC-ND 4.0), permitting only noncommercial, nonderivative use with attribution. All other rights reserved.

Address: Bone Marrow Transplant Department, Great Ormond Street Hospital for Children, London, UK.; Stem Cell Transplantation andCellular Therapies, Department of Pediatrics, Memorial Sloan-Kettering Cancer Center, New York, NY.; Department of Pediatric Oncology, Boston Children's Hospital and Dana-Farber Cancer Institute, Boston, MA.; Stem Cell Transplantation, Department of Pediatric Oncology, Hematology and Hemostasis, University Hospital Leipzig, Leipzig, Germany.; Pediatric Neurology Department, Leukodystrophies Reference Center, Hôpital Universitaire Hôpital Bicêtre-Hôpitaux Universitaires Paris Sud, Paris, France.; Hematology, Oncology and Blood & Marrow Transplantation, Department of Pediatrics, Children's Hospital Los Angeles, Los Angeles, CA.; Division of Pediatric Transplant and Cellular Therapy, Department of Pediatrics, Duke University Medical Center, Durham, NC.; Pediatric Blood and Bone Marrow Transplantation Program, Princess Máxima Center for Pediatric Oncology, Utrecht, the Netherlands.; Department of Pediatrics, University Medical Center Utrecht, UU, Utrecht, the Netherlands.; Paediatric Inborn Errors of Metabolism, Manchester University NHS Foundation Trust, Manchester, UK.; Child Neurology Service, Hospital Universitario Austral, Buenos Aires, Argentina.; Department ofPediatric Hematology and Oncology, Cell and Gene Therapy,Bambino GesùChildren's Hospital,IRRCS, Rome, Italy.; Cellular Therapy and Transplant Section, Division of Oncology, Children's Hospital of Philadelphia, Philadelphia, PA.; Paediatric Oncology and Haematology Department, Hospital Universitari Vall d'Hebron and Vall d'Hebron Institut de Recerca, Barcelona, Spain.; Midwest Radiology, Minneapolis, MN.; bluebird bio, Inc., Cambridge, MA; and.; Blood and Marrow Transplantation Program, Department of Pediatrics, University of Minnesota.
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