Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
. 2024 Jun 1;109(6):1792-1799.
doi: 10.3324/haematol.2023.283826.

Granulocyte transfusions in severe aplastic anemia

Affiliations

Granulocyte transfusions in severe aplastic anemia

Roma V Rajput et al. Haematologica. .

Abstract

Patients with severe aplastic anemia (SAA) are at high risk of morbidity and mortality due to severe infections. We aimed to characterize the role of granulocyte transfusions (GT) in SAA. Primary outcomes were survival after the first GT, including overall survival (OS) at last follow up, survival to discharge, and receipt of a hematopoietic stem cell transplant (HSCT) Secondary outcomes included evaluation of clinical response at 7 and 30 days after initiation of GT, using a clinical scoring system incorporating microbiological and radiographic response. Twenty-eight SAA patients underwent 30 GT courses with a per-dose median of 1.28x109 granulocytes/kilogram (range, 0.45-4.52x109). OS from initial GT to median last follow up (551 days) was 50%, with 39% (11/28) alive at last follow up. Sixty-four percent (18/28) of all patients survived to hospital discharge. Patients with a complete or partial response, or stable infection, at 30 days had significantly better OS compared to non-responders (P=0.0004). Eighty-six percent (18/21) of patients awaiting HSCT during GT underwent a transplant and 62% (13/21) survived to post-HSCT discharge. Sex, type of infection, and percentage of days with absolute neutrophil count >0.2x109/L during the course of GT were not predictive of survival (P=0.52, P=0.7 and P=0.28, respectively). Nine of 28 (32%) patients developed new or increased human leukocyte antigen alloimmunization during their GT course. GT in SAA may have an impact on survival in those patients with improvement or stabilization of their underlying infection. Alloimmunization can occur and OS in this population remains poor, but GT may be a useful tool to bridge patients to curative treatment with HSCT.

PubMed Disclaimer

Figures

Figure 1.
Figure 1.
Overall survival of patients with severe aplastic anemia who received granulocyte transfusions. (A) Overall survival from the initial granulocyte transfusion. (B) Overall survival from the initial granulocyte transfusion based on overall response at 30 days after the granulocyte transfusions. C: complete response; P/S: partial response or stable infection; Pr: progression.

References

    1. Quillen K, Wong E, Scheinberg P, et al. . Granulocyte transfusions in severe aplastic anemia: an eleven-year experience. Haematologica. 2009;94(12):1661-1668. - PMC - PubMed
    1. Wang H, Wu Y, Fu R, et al. . Granulocyte transfusion combined with granulocyte colony stimulating factor in severe infection patients with severe aplastic anemia: a single center experience from China. PLoS One. 2014;9(2):e88148. - PMC - PubMed
    1. Price TH, Boeckh M, Harrison RW, et al. . Efficacy of transfusion with granulocytes from G-CSF/dexamethasone-treated donors in neutropenic patients with infection. Blood. 2015;126(18):2153-2161. - PMC - PubMed
    1. Center for Disease Control and Prevention. The National Healthcare Safety Network (NHSN) Biovigilance Component Hemovigilance Module Surveillance Protocol. https://www.cdc.gov/nhsn/pdfs/biovigilance/bv-hv-protocol-current.pdf. Accessed November 20, 2023.
    1. Valdez JM, Scheinberg P, Nunez O, et al. . Decreased infection-related mortality and improved survival in severe aplastic anemia in the past two decades. Clin Infect Dis. 2011;52(6):726-735. - PMC - PubMed

Publication types