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Peer-reviewed veterinary case report

Dacarbazine treatment for dogs with advanced histiocytic sarcoma

By Kezer, K A et al.·Published in Veterinary and comparative oncology·2018·Department of Clinical Sciences, United States·View original on PubMed

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Original publication title: Efficacy of dacarbazine as a rescue agent for histiocytic sarcoma in dogs.

Species:
dog
Behaviour & energyDogs

Plain-English summary

A group of dogs diagnosed with histiocytic sarcoma (a type of aggressive cancer) received a chemotherapy drug called dacarbazine after their initial treatment with another medication didn't work. Out of 17 dogs, three showed some improvement, with a partial remission rate of about 17.6%. Those that responded to the treatment lived an average of 70 days without worsening symptoms, while the overall survival without progression was about 21 days. Side effects from dacarbazine were generally mild and went away on their own.

People also search for: dog histiocytic sarcoma treatment · dacarbazine for dogs cancer · dog chemotherapy side effects

Abstract

BACKGROUND: Canine histiocytic sarcoma (HS) is an aggressive neoplasm that is generally associated with a poor prognosis. CCNU is considered first-line medical therapy, although the majority of dogs ultimately develop progressive disease. The objective of this study was to evaluate the efficacy of dacarbazine as a rescue agent for HS. MATERIALS AND METHODS: Medical records of dogs diagnosed with HS that received at least one dose of dacarbazine were reviewed. Information collected and analyzed included signalment, disease distribution, treatment history, dacarbazine treatments (including dose, interval and total number of cycles), adverse events, and response to treatment. RESULTS: Seventeen dogs were included, all of which had disseminated or metastatic disease and had received prior treatment with CCNU. Three dogs achieved partial remission for an overall response rate of 17.6%. The overall median event-free survival (EFS) was 21 days. For dogs that experienced an objective response, the EFS was 70 days. Toxicity secondary to dacarbazine was generally mild and self-limiting. CONCLUSION: In the setting of advanced disease, dacarbazine appears to have modest activity against HS and warrants further investigation.

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Original publication on PubMed: https://pubmed.ncbi.nlm.nih.gov/28419676/