Mitotane in Canine Adrenal Disease and Adrenocortical Tumours
- Entry kind
- Generic drug
- Product family
- Adrenocorticolytic agents
Quick summary
mitotane (o,p′-DDD) is covered as adrenocorticolytic agents; hazardous antineoplastic medicine, with species, evidence, regulatory, safety, interaction and monitoring boundaries for a veterinarian-led decision.
What it is
Adrenocorticolytic agents; hazardous antineoplastic medicine. Mitotane.
Active ingredients / formula
Mitotane.
Mechanism / rationale
Mitotane is a DDT derivative with selective cytotoxic effects on adrenal cortical cells and inhibition of steroid production.
How it is discussed in tumor care
Its core veterinary role is adrenal cortical suppression in hyperadrenocorticism and selected adrenocortical tumours. It is not general chemotherapy for unrelated masses and should be linked to endocrine diagnosis and hormone assessment.
Potential role
Its core veterinary role is adrenal cortical suppression in hyperadrenocorticism and selected adrenocortical tumours. It is not general chemotherapy for unrelated masses and should be linked to endocrine diagnosis and hormone assessment.
Typical use context
Oral hazardous medicine under close veterinary endocrine or oncology supervision
Evidence snapshot
Use is established in canine endocrine practice, while evidence for tumour control depends on resectability, functional status and disease extent. Hormone normalisation is not identical to eradication of an adrenal tumour.
Safety notes
Gastrointestinal signs, weakness, central nervous system depression, dermatitis and potentially dangerous adrenal insufficiency are recognised. Over-suppression can become an emergency.
Interactions / cautions
Other glucocorticoid-modifying medicines, surgery, stress, electrolyte disorders and concurrent chemotherapy require coordinated planning. Caregivers need a clinic-issued emergency plan, not a website taper or dose.
Regulatory status
No FDA-approved canine or feline oncology indication was established for this medicine in this audit. In the United States, veterinary oncology use of an approved human or animal formulation is extra-label and must occur under a veterinarian within AMDUCA conditions and a valid VCPR.
Regions, labels and market differences
Multi-region specialist use; product availability, extra-label prescribing law and pharmacy handling vary by jurisdiction.
Monitoring plan
The veterinarian confirms adrenal diagnosis and functional status, reviews electrolytes and organ function and uses hormone testing and clinical signs to guide treatment. Weakness, collapse, vomiting, diarrhoea or loss of appetite can indicate urgent adrenal or drug toxicity.
Questions to ask your veterinarian
- Does the confirmed diagnosis and species match the evidence population?
- What is labelled, conditionally authorised or extra-label in this region?
- Which objective findings will define benefit, toxicity and a change in plan?
- What household handling, waste and urgent-contact instructions apply?