Peer-reviewed veterinary case report
Testing higher doses of vinblastine chemotherapy in dogs with cancer
By Bailey, D B et al.·Published in Journal of veterinary internal medicine·2008·Department of Clinical Sciences, United States·View original on PubMed →
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Original publication title: Phase I dose escalation of single-agent vinblastine in dogs.
- Species:
- dog
Plain-English summary
A group of 23 dogs with lymphoma or skin tumors received a chemotherapy drug called vinblastine to see how much they could tolerate. The starting dose was 3.0 mg/m2, and it was increased to find the maximum safe dosage, which turned out to be 3.5 mg/m2. While most dogs handled the treatment well, some experienced severe drops in white blood cell counts, which can lead to serious infections. Despite this, two dogs showed early signs of improvement in their cancer. The study suggests that vinblastine can be safely given every two weeks, with antibiotics recommended to prevent infections.
People also search for: dog lymphoma treatment · vinblastine dosage for dogs · chemotherapy side effects in dogs
Abstract
BACKGROUND: Vinblastine (VBL) is commonly used in dogs at a dosage of 2.0 mg/m2. The minimal toxicity observed at this dosage indicates that higher dosages might be well tolerated. HYPOTHESIS: The maximum tolerated dosage (MTD) for a single VBL treatment is higher than the previously published dosage of 2.0 mg/m2. ANIMALS: Twenty-three dogs with lymphoma or cutaneous mast cell tumors. METHODS: Dogs received 1 single-agent VBL treatment IV. The starting dosage was 3.0 mg/m2, and dosages were increased in increments of 0.5 mg/m2 in cohorts of 3 dogs. Hematologic toxicity was assessed with weekly CBCs. Gastrointestinal toxicity was assessed from medical histories from owners. Once the MTD was determined, additional dogs were treated with VBL at that dosage. Dogs whose cancers responded to VBL continued to receive treatments q2-3 weeks. RESULTS: VBL dosages ranged from 3.0 to 4.0 mg/m2. Neutropenia was the dose-limiting toxicity, with the nadir identified 7 days after treatment and resolving by 14 days after treatment. The MTD was 3.5 mg/m2. Sixteen dogs were treated at this dosage, and 3 experienced severe toxicity characterized by asymptomatic grade 4 neutropenia, febrile grade 4 neutropenia, and death. Gastrointestinal toxicity was mild and self-limiting. Preliminary evidence of antitumor activity was identified in 2 of 12 dogs with lymphoma treated at the MTD. CONCLUSIONS AND CLINICAL IMPORTANCE: In dogs, single-agent VBL is well tolerated at a dosage of 3.5 mg/m2 IV. At this dosage, the minimum safe treatment interval is q2 weeks, and adjunct treatment with prophylactic antibiotics should be considered.
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Search related cases →Original publication on PubMed: https://pubmed.ncbi.nlm.nih.gov/19000250/