Peer-reviewed veterinary case report
Toceranib phosphate (Palladia) for treating canine carcinomatosis
By Hicks, Kelly A et al.·Published in Veterinary and comparative oncology·2024·Carlson College of Veterinary Medicine, United States·View original on PubMed →
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Original publication title: Retrospective evaluation of toceranib phosphate (Palladia) in the treatment of canine carcinomatosis and mesothelioma.
- Species:
- dog
Plain-English summary
A group of dogs diagnosed with aggressive cancers called carcinomatosis and mesothelioma were treated with a medication called toceranib phosphate (Palladia). Many of these dogs had fluid buildup in their abdomen, which is a common symptom. The treatment showed some effectiveness, with about 30% of the dogs experiencing a reduction in tumor size, and most dogs had stable disease for several months. While some dogs experienced mild side effects like diarrhea or decreased appetite, the treatment was generally well tolerated. On average, dogs lived around 10 months after starting treatment, with some living much longer.
People also search for: dog mesothelioma treatment · toceranib phosphate for dogs · canine carcinomatosis prognosis
Abstract
Canine carcinomatosis (CC) and mesothelioma (CM) are rare but aggressive neoplasms that historically have been associated with poor prognoses. There is limited information regarding treatment for CC and CM. The purpose of this retrospective study was to evaluate the efficacy and tolerability of toceranib phosphate (Palladia) in dogs with CC and CM. Cases were solicited from the American College of Veterinary Internal Medicine (ACVIM) Oncology listserv and retrospectively reviewed. For eligibility, a cytologic and/or histopathologic diagnosis of CC or CM was required. A total of 23 cases were included (CC = 14, CM = 8, both = 1). Eighty-two percent (19/23) of dogs presented with effusion. The best overall response rate (BORR) was 30.4% (13% complete response [CR], 17.3% partial response [PR]). Stable disease (SD) was appreciated in 14 dogs (60.8%) including the four dogs without effusion. The most common toceranib-related adverse events were either Grade 1 and 2 diarrhea or hyporexia. The median progression-free survival (PFS) was 171 days (range, 7-519 days) and overall median survival time (MST) was 301 days (range, 49-875 days) for all dogs. When evaluating dogs solely with effusion, the median PFS and overall MST were 171 days (range, 7-519 days) and 285 days (range, 49-875 days), respectively. This report demonstrates that toceranib is both well tolerated and a potential treatment for CC and CM. A randomised, controlled, prospective study would be needed to objectively assess the survival benefit of toceranib in the management of CC and CM, with and without effusion.
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Search related cases →Original publication on PubMed: https://pubmed.ncbi.nlm.nih.gov/38622074/