Peer-reviewed veterinary case report
Survival rates in dogs with mast cell tumors treated with masitinib
By Hahn, Kevin A et al.·Published in American journal of veterinary research·2010·Gulf Coast Veterinary Specialists, United States·View original on PubMed →
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Original publication title: Evaluation of 12- and 24-month survival rates after treatment with masitinib in dogs with nonresectable mast cell tumors.
- Species:
- dog
Plain-English summary
A group of 132 dogs with nonresectable mast cell tumors (a type of skin cancer) were treated with a medication called masitinib to see how it affected their survival. After 12 months, about 62% of the dogs receiving masitinib were still alive, compared to only 36% of those given a placebo. By 24 months, the survival rates were 40% for the masitinib group versus 15% for the placebo group. The study found that controlling the tumors after 6 months was a good indicator of longer survival, suggesting that masitinib can be an effective treatment for these tumors in dogs.
People also search for: dog mast cell tumor treatment · masitinib for dogs · dog skin cancer survival rates
Abstract
OBJECTIVE: To evaluate the effectiveness of masitinib for the treatment of nonresectable mast cell tumors (MCTs) in dogs at 12 and 24 months after onset of treatment. ANIMALS: 132 dogs with nonresectable grade 2 or 3 MCTs. PROCEDURES: Dogs received masitinib (12.5 mg/kg/d, PO; n = 106) or a placebo (26). After 6 months, treatment was extended with tumor assessments at 3-month intervals until detection of disease progression. Endpoints were tumor response and overall survival rate and time. RESULTS: In dogs with nonresectable MCTs, masitinib significantly improved survival rate, compared with results for the placebo, with 59 of 95 (62.1%) and 9 of 25 (36.0%) dogs alive at 12 months and 33 of 83 (39.8%) and 3 of 20 (15.0%) dogs alive at 24 months, respectively. Median overall survival time was 617 and 322 days, respectively. Tumor control at 6 months had a high predictive value for 24-month survival, with high specificity (88%) and sensitivity (76%), whereas short-term tumor response (within 6 weeks) had a poor predictive value. Complete responses at 24 months were observed in 6 of 67 (9.0%) dogs with nonresectable MCTs treated with masitinib. CONCLUSIONS AND CLINICAL RELEVANCE: Masitinib significantly increased survival rates at 12 and 24 months in dogs with nonresectable MCTs. Control of disease at 6 months, but not best response at 6 weeks, was predictive of long-term survival in dogs treated with masitinib, which suggested that short-term response may be irrelevant for assessing clinical efficacy of tyrosine kinase inhibitors for treatment of MCTs.
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Search related cases →Original publication on PubMed: https://pubmed.ncbi.nlm.nih.gov/21034327/