Peer-reviewed veterinary case report
DNA vaccine treatment for malignant melanoma on dogs' toes
By Manley, C A et al.·Published in Journal of veterinary internal medicine·2011·Donaldson-Atwood Cancer Clinic, United States·View original on PubMed →
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Original publication title: Xenogeneic murine tyrosinase DNA vaccine for malignant melanoma of the digit of dogs.
- Species:
- dog
Plain-English summary
A group of 58 dogs with malignant melanoma on their toes received a new DNA vaccine designed to help their immune system fight the cancer. The dogs who were treated with this vaccine, along with other local treatments, had a median survival time of about 476 days, and many lived for over a year. Those without metastasis (spread of cancer) had a much better outcome, surviving an average of 533 days compared to just 105 days for those with metastasis. The vaccine was found to be safe and could be a promising option for treating this aggressive cancer in dogs.
People also search for: dog melanoma treatment · canine cancer vaccine · dog toe tumor survival rate
Abstract
BACKGROUND: Malignant melanoma of dogs is a highly aggressive neoplasm and is the 2nd most common digit tumor. Metastatic disease is a common sequela for which few effective treatment options exist. Studies show that xenogeneic tyrosinase DNA vaccination yields immune responses and prolongation of survival in dogs with oral malignant melanoma. OBJECTIVES/HYPOTHESIS: Describe clinical findings and tumor characteristics of a cohort of dogs with digit malignant melanoma, and evaluate the prognostic utility of a proposed staging system. Determine if a novel xenogeneic DNA vaccine is safe and potentially effective for treatment of dogs with digit melanoma. ANIMALS: Fifty-eight dogs with digit malignant melanoma treated at the Animal Medical Center between 2004 and 2007. METHODS: Retrospective, medical records review of dogs with digit melanoma treated with xenogeneic DNA vaccine. RESULTS: Overall median survival time (MST) for dogs treated with loco-regional control and xenogeneic DNA vaccine was 476 days with a 1-year survival rate of 63%. MST for dogs presenting with metastasis was 105 days versus 533 days for dogs presenting without metastasis (P < .0001). Forty-eight percent of the dogs in the latter group were alive at 2 and 3 years. A proposed staging system proved prognostic with stages I-IV dogs surviving >952, >1,093, 321, and 76 days, respectively. CONCLUSIONS AND CLINICAL IMPORTANCE: The xenogeneic murine tyrosinase DNA vaccine was safe and appears effective when used in conjunction with local and regional disease control. The proposed staging system was prognostic in this study and future studies might benefit from utilizing this staging system.
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Search related cases →Original publication on PubMed: https://pubmed.ncbi.nlm.nih.gov/21143299/