NYMC Faculty Publications

DOI

10.1038/bmt.2016.265

Journal Title

Bone Marrow Transplantation

First Page

400

Last Page

408

Document Type

Article

Publication Date

3-1-2017

Department

Pediatrics

Keywords

Acute Disease, Adolescent, Antilymphocyte Serum administration & dosage, Child, Preschool child, Chronic DiseaseCord Blood Stem Cell Transplantation, Disease-Free Survival, Female, Graft vs Host Disease etiology, Graft vs Host Disease mortality, Graft vs Host Disease prevention & control, Humans, Newborn Infant, Leukemia mortality, Leukemia therapy, Male, Registries, Survival Rate, Transplantation Conditioning, antilymphocyte serum, multicenter study, clinical trial

Disciplines

Medicine and Health Sciences

Abstract

Using the Center for International Blood and Marrow Transplant Research (CIBMTR) registry, we analyzed 1404 umbilical cord bloodtransplantation (UCBT) patients (single (<18 years)=810, double (⩾18 years)=594) with acute leukemia to define the incidence of acuteGvHD (aGvHD) and chronic GvHD (cGvHD), analyze clinical risk factors and investigate outcomes. After single UCBT, 100-day incidence of grade II-IV aGvHD was 39% (95% confidence interval (CI), 36-43%), grade III-IV aGvHD was 18% (95% CI, 15-20%) and 1-year cGvHD was 27% (95% CI, 24-30%). After double UCBT, 100-day incidence of grade II-IV aGvHD was 45% (95% CI, 41-49%), grade III-IV aGvHD was 22% (95% CI, 19-26%) and 1-year cGvHD was 26% (95% CI, 22-29%). For single UCBT, multivariate analysis showed that absence of antithymocyte globulin (ATG) was associated with aGvHD, whereas prior aGvHD was associated with cGvHD. For double UCBT, absence of ATG and myeloablative conditioning were associated with aGvHD, whereas prior aGvHD predicted for cGvHD. Grade III-IV aGvHD led to worse survival, whereas cGvHD had no significant effect on disease-free or overall survival. GvHD is prevalent after UCBT with severe aGvHD leading to higher mortality. Future research in UCBT should prioritize prevention of GvHD.

Comments

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Publisher's Statement

This is a post-peer-review, pre-copyedit version of an article published in Bone Marrow Transplantation. The final authenticated version is available online at: https://doi.org/10.1038/bmt.2016.265

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