Peer-reviewed veterinary case report
Toceranib treatment results for dogs with high-risk adrenal tumors
By Chalfon, C et al.·Published in The Journal of small animal practice·2025·Centro Veterinario Torinese, Italy·View original on PubMed →
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Original publication title: Toceranib phosphate for the treatment of dogs with high-risk adrenal gland tumours: 16 cases (2019-2023).
- Species:
- dog
Plain-English summary
Sixteen dogs with high-risk adrenal gland tumors, including adrenocortical carcinoma and pheochromocytoma, were treated with a medication called toceranib phosphate. Most dogs with pheochromocytoma showed improvement, with many maintaining stable disease for several months. Half of the dogs with adrenocortical carcinoma were euthanized due to disease progression, while the other half remained healthy and cancer-free for over a year after starting treatment. Overall, toceranib was well-tolerated and may help improve outcomes for dogs with these serious tumors.
People also search for: dog adrenal gland tumor treatment · toceranib for dogs · pheochromocytoma in dogs · adrenocortical carcinoma prognosis
Abstract
OBJECTIVES: The aims of this study were to evaluate the response rate, time to progression (TTP) and survival times of dogs with high-risk adrenal gland tumours (ATs) treated with toceranib phosphate, in both macroscopic and microscopic setting, and to report the adverse event (AE) profiles. MATERIALS AND METHODS: Medical records of dogs diagnosed with a high-risk adrenocortical carcinoma (ACC) or phaeochromocytoma (PCC), treated with toceranib, were retrospectively reviewed. High-risk ATs were defined as inoperable and/or metastatic ATs or cortical tumours with high Utrecht score. Endpoints were response rate, TTP and overall progression-free survival time (PFST). Adverse events were reported according to VCOG-CTCAE. RESULTS: Sixteen dogs were included: 10 diagnosed with PCC and six with ACC. All dogs with ACC received adjuvant toceranib due to a high Utrecht score or metastatic disease, while all dogs with PCC were treated with toceranib in the macroscopic setting. A clinical benefit was detected in 80% of dogs with PCC: four achieved stable disease for a median TTP of 176.5 days, and two achieved partial response for 182 and >100 days, respectively. Median PFST for dogs with PCC was 112 days. Among dogs with ACC, 3 (50%) progressed and were euthanized after 237, 364 and 273 days; the remaining 3 (50%) dogs were alive and disease free 382, 508 and 583 days after starting toceranib. Overall, toceranib was well-tolerated. CLINICAL SIGNIFICANCE: Toceranib may offer clinical benefit and improve outcome in dogs with high-risk ATs in both the macroscopic and microscopic disease setting.
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Search related cases →Original publication on PubMed: https://pubmed.ncbi.nlm.nih.gov/39973216/