Variables Affecting Outcomes After Allogeneic Hematopoietic Stem Cell Transplant for Cerebral Adrenoleukodystrophy

Author:

Chiesa Robert1,Boelens Jaap Jan2ORCID,Duncan Christine N3,Kuehl Joern-Sven4,Sevin Caroline5,Kapoor Neena6,Prasad Vinod K7ORCID,Lindemans Caroline A.8,Jones Simon A.9,Amartino Herman M.10,Algeri Mattia11,Bunin Nancy J.12,Diaz de Heredia Cristina13ORCID,Loes Daniel J.14,Shamir Esther15,Timm Alison15,McNeil Elizabeth16,Dietz Andrew C15,Orchard Paul J.14ORCID

Affiliation:

1. Great Ormond Street Hospital, London, United Kingdom

2. Memorial Sloan Kettering Cancer Center, New York, New York, United States

3. Dana-Farber Cancer Institute, Boston, Massachusetts, United States

4. Pediatric Oncology, Hematology and Hemostaseology, University Hospital Leipzig, Leipzig, Germany

5. Hôpital Universitaire Hôpital Bicêtre-Hôpitaux Universitaires Paris Sud, Le Kremlin-Bicêtre, France

6. USC Childrens Hospital Los Angeles, Los Angeles, California, United States

7. Duke University Medical Center, Durham, North Carolina, United States

8. Prinses maxima Center and University Medical Center Utrecht, Utrecht, Netherlands

9. Manchester university NHS foundation trust, Manchester, United Kingdom

10. Hospital Universitario Austral, Buenos Aires, Argentina

11. IRCCS Bambino Gesù Children's Hospital, Rome, Italy

12. Children's Hospital of Philadelphia, Philadelphia, Pennsylvania, United States

13. Hospital Vall dï¿1/2Hebron, Barcelona, Spain

14. University of Minnesota, Minneapolis, Minnesota, United States

15. bluebird bio, Inc., Cambridge, Massachusetts, United States

16. Passage Bio, United States

Abstract

Allogeneic hematopoietic stem cell transplantation (allo-HSCT) in early cerebral adrenoleukodystrophy (CALD) 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 two 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%) versus AD (41%) cohort (p=0.015) and comparable between ED1 and ED2 cohorts (p=0.991). The stabilization of neurologic function post-transplant was greater in the ED versus AD cohort, with a median change from baseline at 24 months post-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 AD (22%) cohort, however the difference was not significant (p=0.094). Transplant-related safety outcomes were also impacted by transplant-related characteristics: graft failure incidence was significantly higher with unrelated umbilical cord grafts versus matched related donors (MRD) (p=0.039), and acute GVHD and graft failure incidences varied by conditioning regimen. The study is registered to https://clinicaltrials.gov as NCT02204904.

Publisher

American Society of Hematology

Subject

Hematology

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