G-CSF and G-CSF-related vasculitis: a systematic review of the literature and intriguing future research perspectives

Future Oncol. 2021 Nov;17(33):4619-4634. doi: 10.2217/fon-2021-0701. Epub 2021 Aug 25.

Abstract

Background: There are several case reports suggesting that G-CSFs may, in rare conditions, produce serious side effects, such as vasculitis. Materials & methods: A systematic search was conducted in Medline via PubMed, Embase and Cochrane Library to describe this unusual side effect to raise awareness among clinicians for early recognition and treatment. Results: Fifty-seven patients were analyzed. The most prevalent cancer type was breast cancer (47%). Long-acting G-CSF was used in 38 patients (67%). Only 47% of patients were treated with steroids. Conclusion: Although the benefit of G-CSF treatment outweighs the potential damage, oncologists should consider the possibility of triggering a vascular toxicity and try to identify patients at increased risk for this side effect.

Keywords: G-CSF; G-CSF-related vasculitis; IL-6; antineutrophil cytoplasmic antibodies; neutropenia recovery; neutrophil; review; side effect.

Plain language summary

Lay abstract Background: Several case reports suggest that a type of drug called granulocyte colony-stimulating factor (G-CSFs) may, in rare cases, produce serious side effects, such as vasculitis. Materials & methods: A systematic search was conducted to describe this unusual side effect. Results: Fifty-seven patients were analyzed. The most prevalent cancer type in which this side effect was observed was breast cancer (47%). Only 47% of patients were treated with steroids. The main symptoms, such as fever, chest/epigastric pain and general malaise, are nonspecific and cannot be used to diagnose the side effect; laboratory findings are suggestive of inflammation. Conclusion: Accurate assessment of what causes this adverse event is extremely important. Although the benefit of G-CSF treatment outweighs the potential damage, oncologists should consider the possibility of triggering vascular toxicity and try to identify patients at increased risk.

Publication types

  • Systematic Review

MeSH terms

  • Antineoplastic Combined Chemotherapy Protocols / adverse effects*
  • Chemotherapy-Induced Febrile Neutropenia / drug therapy*
  • Diagnosis, Differential
  • Filgrastim / administration & dosage
  • Filgrastim / adverse effects*
  • Glucocorticoids / administration & dosage
  • Glucocorticoids / adverse effects
  • Humans
  • Neoplasms / blood
  • Neoplasms / drug therapy*
  • Polyethylene Glycols / administration & dosage
  • Polyethylene Glycols / adverse effects*
  • Vasculitis / chemically induced*
  • Vasculitis / diagnosis
  • Vasculitis / epidemiology
  • Vasculitis / prevention & control

Substances

  • Glucocorticoids
  • pegfilgrastim
  • Polyethylene Glycols
  • Filgrastim