Publication

Peritransplantation Red Blood Cell Transfusion Is Associated with Increased Risk of Graft-versus-Host Disease after Allogeneic Hematopoietic Stem Cell Transplantation

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Last modified
  • 05/22/2025
Type of Material
Authors
    Sakura Hosoba, Emory UniversityEdmund K Waller, Emory UniversityNeeta Shenvi, Emory UniversityMichael Graiser, Emory UniversityKirk Easley, Emory UniversityZaid Al-Kadhimi, Emory UniversityAkira Andoh, Shiga University of Medical ScienceAna G Antun, Emory UniversitySheliagh Barclay, Emory UniversityCassandra D Josephson, Emory UniversityJean Louise Koff, Emory UniversityH.Jean Khoury, Emory UniversityAmelia A Langston, Emory UniversityJames Zimring, Emory UniversityJohn D Roback, Emory UniversityCynthia R Giver, Emory University
Language
  • English
Date
  • 2018-05-01
Publisher
  • Elsevier: 12 months
Publication Version
Copyright Statement
  • © 2018 The American Society for Blood and Marrow Transplantation
License
Final Published Version (URL)
Title of Journal or Parent Work
ISSN
  • 1083-8791
Volume
  • 24
Issue
  • 5
Start Page
  • 973
End Page
  • 982
Grant/Funding Information
  • This study received funding from NIH NHLBI Program Project Grant P01 HL086773
Supplemental Material (URL)
Abstract
  • More than 90% of allogeneic hematopoietic stem cell transplantation (allo-HSCT) recipients receive red blood cell (RBC) or platelet transfusions in the peritransplantation period. We tested the hypothesis that transfusions are associated with the development of severe (grade III-IV) acute graft-versus-host disease (aGVHD) or mortality after allo-HSCT in a retrospective study of 322 consecutive patients receiving an allogeneic bone marrow or granulocyte colony-stimulating factor-mobilized blood stem cell graft for a hematologic malignancy. Counting transfused RBC and platelet units between day −7 pretransplantation and day +27 post-transplantation, but excluding transfusions administered after a diagnosis of aGVHD, yielded medians of 5 RBC units and 2 platelet units transfused. Sixty-three patients (20%) developed a maximal grade III-IV aGVHD with onset up to day +150 post-transplantation (median aGVHD onset of 28 days). HLA mismatch (hazard ratio [HR], 2.4; 95% confidence interval [CI], 1.2 to 4.7; P =.01), and transfusion of more than the median number of RBC units (HR, 2.1; 95% CI, 1.1 to 3.7; P =.02) were independently associated with greater risk of grade III-IV aGVHD in a multivariable analysis model. Disease risk strata (HR, 1.7; 95% CI, 1.2 to 2.4 for high risk versus low risk; P =.005) and transfusion of more than the median number of RBC units (HR, 1.4; 95% CI, 1.0 to 2.0; P =.054) were independently associated with inferior overall survival. These data support our hypothesis that peritransplantation RBC transfusions are associated with the risk of developing severe aGVHD and worse overall survival following allo-HSCT, and suggest that strategies to reduce routine RBC transfusion may favorably reduce the incidence and severity of GVHD.
Author Notes
  • Cynthia R. Giver, Emory Winship Cancer Institute, Hematology and Medical Oncology, 1365B Clifton Road NE, Suite B5106, Atlanta, GA 30322, Tel: 404-778-5806, Fax: 404-778-3110, cgiver@emory.edu.
Keywords
Research Categories
  • Health Sciences, Medicine and Surgery
  • Health Sciences, Pathology

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