Lomustine (CCNU) In Dogs & Cats: Uses, Dosage and Side Effects
Overview
- Interferes with the synthesis and function of DNA, RNA and proteins.
- Antitumour activity correlates best with formation of interstrand cross-linking of DNA.
- Lomustine is highly lipid-soluble, allowing rapid transport across the blood–brain barrier.
Uses of Lomustine (CCNU)
- Reported to have some efficacy in the treatment of brain tumours, mast cell tumours, refractory lymphoma, histiocytic sarcoma and epitheliotrophic lymphoma.
- Component of the modified CHOP protocol for treatment of T-cell lymphoma.
Dose of Lomustine (CCNU) in Dogs and Cats
Dogs:
- All uses: 60–80 mg/m2 p.o. q3–4wk.
Cats:
- All uses: A dose of 30–60 mg/m2 p.o. q4–6wk has been suggested but is not well established.
- If using this drug in the cat, specialist advice should be sought, as dosing intervals may need to be increased.
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Side Effects of Lomustine (CCNU) in Dogs and Cats
- Myelosuppression is the dose-limiting toxicity, with neutropenia developing 7–14 days after administration (although the onset of myelosuppression can range from 1–6 weeks and can be particularly delayed in cats).
- Neutropenia may be severe and life-threatening at the higher end of the dose range in some dogs.
- Thrombocytopenia can also be seen, often with no other concurrent cytopenias.
- GI and cumulative dose-related and potentially irreversible hepatic toxicity have been reported in the dog.
Contraindications of Lomustine (CCNU) in Dogs and Cats
- Bone marrow suppression.
- Pre-existing liver disease.
Some Notes:
- Do not use it with other myelosuppressive agents.
- Lomustine requires hepatic microsomal enzyme hydroxylation for the production of antineoplastic metabolites.
- It should be used with caution in dogs being treated with agents that induce liver enzyme activity, e.g. phenobarbital.
- In humans, cimetidine enhances the toxicity of lomustine.
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