Cyclophosphamide: Uses, Dosage and Side Effects
Overview
Cross-linking of DNA by metabolic byproducts inhibits both DNA synthesis and its activity.
Uses of Cyclophosphamide
- Treatment of lymphoproliferative and myeloproliferative diseases.
- May play a role in the treatment of certain sarcomas and carcinomas when used in metronomic chemotherapy protocols.
Dose of Cyclophosphamide in Dogs and Cats
Dogs:
- Lymphoid neoplasia: generally 50 mg/m2 p.o. q48h or 3–4 consecutive days/week; or 200–250 mg/m2 p.o or i.v. q3wk.
- Metronomic chemotherapy: 10–15 mg/m2 p.o. q24h.
- Multiple myeloma in patients refractory to melphalan: 1 mg/kg p.o. q24h.
- Macroglobulinaemia in patients refractory to chlorambucil: 1 mg/kg p.o. q24h.
Cats:
Lymphoid neoplasia: as for dogs, except 200–300 mg/m2 in ‘high dose’ COP regimes.
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Side Effects of Cyclophosphamide in Dogs and Cats
- Myelosuppression, with the nadir usually 5–14 days after therapy so, WBC monitoring is advised.
- A cyclophosphamide metabolite (acrolein) can induce sterile hemorrhagic cystitis.
- Persistent cystitis can cause bladder fibrosis and transitional cell carcinoma.
- Water consumption and furosemide can lower this risk by increasing urine production.
- Vomiting, diarrhea, hepatotoxicity, nephrotoxicity, pulmonary infiltrates and fibrosis, and hair growth reduction are also consequences.
Contraindications of Cyclophosphamide in Dogs and Cats
No information is available.
Some Notes:
- Use with caution in patients with kidney failure; the dose may need to be lowered.
- Cyclophosphamide is no longer recommended as a drug to suppress the immune system.
- Concomitant thiazide diuretics increase myelosuppression risk.
- Oral digoxin absorption may reduce days after dosing.
- Barbiturates enhance cyclophosphamide toxicity by metabolizing faster.
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