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Peer-reviewed veterinary case report

Chemotherapy for nasal tumors in 29 dogs using carboplatin

By Woodruff, Matthew J et al.·Published in Veterinary and comparative oncology·2019·Department of Medicine, Australia·View original on PubMed

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Original publication title: Canine intranasal tumours treated with alternating carboplatin and doxorubin in conjunction with oral piroxicam: 29 cases.

Species:
dog

Plain-English summary

A group of dogs with confirmed intranasal tumors received a combination of chemotherapy drugs, carboplatin and doxorubicin, along with oral piroxicam, to see how well it would work as a treatment. The dogs showed varying survival times, with those having adenocarcinoma or carcinoma living an average of about 280 days, while some types of tumors had shorter survival times. Most dogs tolerated the treatment well, although some experienced side effects. This study suggests that chemotherapy could be a beneficial option for dogs with certain types of intranasal tumors.

People also search for: dog nasal tumor treatment · chemotherapy for dog cancer · intranasal tumor survival rate in dogs

Abstract

Few veterinary studies have evaluated the response to chemotherapy treatment of canine intranasal tumours, while many have focused on the efficacy of radiation therapy. Given the higher costs and limited access to radiation therapy, alternative treatment options are needed. The study describes a cohort of dogs with histologically confirmed intranasal tumours treated with chemotherapy as a sole therapy. This retrospective study was conducted using data from the Melbourne Veterinary Specialist Centre (MVSC) database between 2004 and 2017. Dogs with a histologically confirmed intranasal tumour who received chemotherapy treatment were included. Signalment, presenting signs, tumour type, chemotherapy details, adverse events (AEs) and survival times were reviewed. Twenty-nine dogs met the inclusion criteria. Overall median survival time for dogs in the study was 234 days (range 12-1698 days). Median survival for dogs with adenocarcinoma or carcinoma (n = 12) was 280 days, transitional cell carcinoma (n = 6) 163 days, squamous cell carcinoma, anaplastic carcinoma or undifferentiated carcinoma (n = 7) 59 days and all sarcomas (n = 4) 448 days. Adverse events were reported following 28% of treatments and 69% of dogs experienced at least one AE. Twenty four per cent of all dogs experienced grade 3 or 4 toxicities. The chemotherapy protocol was generally well tolerated. The study suggests potential benefit in the use of chemotherapy for dogs with adenocarcinoma, carcinoma and sarcoma.

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Original publication on PubMed: https://pubmed.ncbi.nlm.nih.gov/30146732/