Balancing Benefits and Risks: A Literature Review on Hypersensitivity Reactions to Human G-CSF (Granulocyte Colony-Stimulating Factor)

Int J Mol Sci. 2024 Apr 28;25(9):4807. doi: 10.3390/ijms25094807.

Abstract

Human granulocyte colony-stimulating factor (G-CSF) is a granulopoietic growth factor used in the treatment of neutropenia following chemotherapy, myeloablative treatment, or healthy donors preparing for allogeneic transplantation. Few hypersensitivity reactions (HRs) have been reported, and its true prevalence is unknown. We aimed to systematically characterize G-CSF-induced HRs while including a comprehensive list of adverse reactions. We reviewed articles published before January 2024 by searching in the PubMed, Embase, Cochrane Library, and Web of Science databases using a combination of the keywords listed, selected the ones needed, and extracted relevant data. The search resulted in 68 entries, 17 relevant to our study and 7 others found from manually searching bibliographic sources. A total of 40 cases of G-CSF-induced HR were described and classified as immediate (29) or delayed (11). Immediate ones were mostly caused by filgrastim (13 minimum), with at least 9 being grade 5 on the WAO anaphylaxis scale. Delayed reactions were mostly maculopapular exanthemas and allowed for the continuation of G-CSF. Reactions after first exposure frequently appeared and were present in at least 11 of the 40 cases. Only five desensitization protocols have been found concerning the topic at hand in the analyzed data. We believe this study brings to light the research interest in this topic that could benefit from further exploration, and propose regular updating to include the most recently published evidence.

Keywords: G-CSF/granulocyte colony-stimulating factor; allergy; anaphylaxis; drug hypersensitivity reactions; filgrastim; hypersensitivity; lenograstim.

Publication types

  • Review

MeSH terms

  • Drug Hypersensitivity* / epidemiology
  • Drug Hypersensitivity* / etiology
  • Granulocyte Colony-Stimulating Factor* / adverse effects
  • Granulocyte Colony-Stimulating Factor* / therapeutic use
  • Humans

Substances

  • Granulocyte Colony-Stimulating Factor

Grants and funding

Publication of this paper was supported by the University of Medicine and Pharmacy Carol Davila through the institutional program Publish not Perish.