Peer-reviewed veterinary case report
Safety of gemcitabine and carboplatin chemo in cats with carcinomas
By Martinez-Ruzafa, I et al.·Published in Journal of veterinary internal medicine·2009·Department of Small Animal Clinical Sciences, United States·View original on PubMed →
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Original publication title: Tolerability of gemcitabine and carboplatin doublet therapy in cats with carcinomas.
- Species:
- cat
Plain-English summary
A group of 20 cats with cancer received a combination of two chemotherapy drugs, gemcitabine and carboplatin, to see how well they tolerated the treatment. Some cats experienced serious side effects like low white blood cell counts and gastrointestinal issues, but overall, the combination was moderately well tolerated. One cat with pancreatic cancer had a complete response to the treatment, while another with squamous cell carcinoma showed partial improvement. The study suggests that while this treatment can be used, exploring different schedules or combinations may be beneficial for better outcomes.
People also search for: cat cancer treatment options · gemcitabine side effects in cats · carboplatin for cats with tumors
Abstract
BACKGROUND: This study was performed to determine the toxicity of gemcitabine-carboplatin doublet therapy in cats with carcinomas. HYPOTHESIS: Gemcitabine and carboplatin are safe in tumor-bearing cats. ANIMALS: Twenty cats with spontaneously occurring carcinomas. METHODS: A cohort of 6 cats received gemcitabine (2 mg/kg IV) on days 1, 8, and 15 and carboplatin (10 mg/kg IV) immediately after gemcitabine on day 1 of a 21-day cycle. A 2nd cohort of 14 cats received carboplatin 4 hours after gemcitabine on day 1 and gemcitabine on day 8 but not day 15. The cycles were repeated every 21 days. RESULTS: Cats in the 1st cohort received a median of 3.75 cycles per animal (range, 1-6). Two cats (33.3%) developed grade 3 or 4 neutropenia, 1 (16.7%) grade 4 thrombocytopenia, and 1 (16.7%) grade 3 gastrointestinal toxicity. Gemcitabine dose reductions and treatment delays occurred in 1 and 4 cats, respectively. Cats in the 2nd cohort received a median of 2 cycles per animal (range, 0.5-10). Two cats (14.3%) had grade 3 or 4 neutropenia and 1 (7.1%) had grade 3 and 4 gastrointestinal toxicity. One cat required gemcitabine dose reduction and 6 had treatment delays. In the 2nd cohort, of 11 cats with measurable tumors, there was 1 complete response (pancreatic carcinoma) and 1 partial response (squamous cell carcinoma, receiving concurrent nonsteroidal anti-inflammatory drugs). CONCLUSIONS AND CLINICAL IMPORTANCE: Gemcitabine-carboplatin combination appears moderately well tolerated in tumor-bearing cats. Minimal patient benefit suggests that alternative schedules or combinations of gemcitabine with other agents should be explored.
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Search related cases →Original publication on PubMed: https://pubmed.ncbi.nlm.nih.gov/19298611/