Cj. Henry et al., VETERINARY USES OF RECOMBINANT HUMAN GRANULOCYTE-COLONY-STIMULATING FACTOR - PART I - ONCOLOGY, The Compendium on continuing education for the practicing veterinarian, 20(6), 1998, pp. 728
Recombinant human granulocyte colony-stimulating factor (rhG-CSF) caus
es an initial increase in leukocyte counts:in small animals. A subsequ
ent decline in leukocyte count is attributed to the development-dt neu
tralizing antibody to the rhG-CSF. According to the findings presented
in this article, however, neutralizing antibodies against rhG-CSF did
not develop in dogs or cats that received chemotherapy. Consequently,
rhG-CSF might be useful for ameliorating chemotherapy-induced myelosu
ppression in small animals, thus permitting more aggressive chemothera
py protocols. Until further studies are completed, veterinarians shoul
d avoid administering rhG-CSF within 24 hours before or after chemothe
rapy. Giving the agent when neutrophil counts are less than,1000 cells
/mu l is Sufficient to decrease the severity of myelosuppression. Shor
t courses (three to six doses) may be sufficient to treat patients wit
h severe myelosuppression. Long-term administration of rhG-CSF to norm
al dogs and cats might lead to the formation of antibodies to endogeno
us granolocyte colony-stimulating factor (G-CSF). Clients should be in
formed about the cost of therapy (approximately $0.72/mu g) versus the
potential risks of withholding therapy.The; true-risks of withholding
G-CSF therapy from neutropenic animals will not be clear until contro
lled randomized studies that involve tumor-bearing animals: are comple
ted. the first part of this two-part article discusses the history of
GL-CSF use in veterinary medicine and considers recommendations for ad
ministering G-CSF to chemotherapy patients. Part II will deal with the
use of G-CSF in patients with infectious disease, such as canine parv
ovirus.