Impact of center volume on outcomes in allogeneic hematopoietic cell transplantation for children
- PMID: 40211066
- PMCID: PMC12151867
- DOI: 10.1038/s41409-025-02569-3
Impact of center volume on outcomes in allogeneic hematopoietic cell transplantation for children
Abstract
The impact of center volume on outcomes in pediatric hematopoietic cell transplantation (HCT) is not well established. We retrospectively analyzed data from a nationwide registry, including 6966 pediatric patients who underwent their first allogeneic HCT at 123 centers in Japan between 2001 and 2020. Centers were categorized by transplant volume as low volume centers (C1, the smallest number of transplantation), medium-low volume centers (C2), medium-high volume centers (C3), and high volume centers (C4, the greatest number of transplantation), and outcomes were compared across these categories. The analysis revealed no statistically significant differences in HCT outcomes among center categories. The 5-year OS by center category was 66.8% (95% CI 64.4-69.0%) for C1, 66.8% (95% CI 64.5-69.0%) for C2, 67.9% (95% CI 65.6-70.2%) for C3, and 68.3% (95% CI 65.9-70.6%) for C4. These results were consistent even when analysis was restricted to malignant and nonmalignant diseases. Our findings suggest that, unlike in adult HCT, outcomes for pediatric HCT are not significantly affected by center volume. These results indicate the consistent quality of care across centers, supporting the accessibility of HCT at various institutions for pediatric patients.
© 2025. The Author(s).
Conflict of interest statement
Competing interests: The authors declare no competing interests.
Figures
References
-
- Kato M. Recent progress in pediatric lymphoblastic leukemia. Int J Hematol. 2023;117:155–61. - PubMed
-
- Bacigalupo A. How I treat acquired aplastic anemia. Blood. 2017;129:1428–36. - PubMed
-
- Vallee TC, Glasmacher JS, Buchner H, Arkwright PD, Behrends U, Bondarenko A, et al. Wiskott-Aldrich syndrome: a study of 577 patients defines the genotype as a biomarker for disease severity and survival. Blood. 2024;143:2504–16. - PubMed
-
- Goebel GA, de Assis CS, Cunha LAO, Minafra FG, Pinto JA. Survival after hematopoietic stem cell transplantation in severe combined immunodeficiency (SCID): a worldwide review of the prognostic variables. Clin Rev Allergy Immunol. 2024;66:192–209. - PubMed
Publication types
MeSH terms
Grants and funding
LinkOut - more resources
Full Text Sources
Miscellaneous
