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Peer-reviewed veterinary case report

Safety and blood levels of taurolidine in dogs with bone cancer

By Marley, Kevin et al.·Published in Journal of experimental & clinical cancer research : CR·2013·View original on PubMed

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Original publication title: Pharmacokinetic study and evaluation of the safety of taurolidine for dogs with osteosarcoma.

Species:
dog
OsteosarcomaMovement & jointsDogs

Plain-English summary

A group of dogs with osteosarcoma (a type of bone cancer) were treated with taurolidine, a drug that has shown promise in fighting this disease. The study found that taurolidine was safe for healthy dogs, but when combined with doxorubicin (a common cancer drug), it led to some serious side effects like heart and kidney issues. However, when taurolidine was used with carboplatin, another chemotherapy drug, it appeared to be safer. Overall, while taurolidine may not be suitable with doxorubicin, it could be a safer option when paired with carboplatin for dogs battling osteosarcoma.

People also search for: dog osteosarcoma treatment · taurolidine for dogs cancer · doxorubicin side effects in dogs

Abstract

BACKGROUND: Osteosarcoma in dogs and humans share many similarities and the dog has been described as an excellent model to study this disease. The median survival in dogs has not improved in the last 25 years. Taurolidine has been shown to be cytotoxic to canine and human osteosarcoma in vitro. The goals of this study were to determine the pharmacokinetics and safety of taurolidine in healthy dogs and the safety of taurolidine in combination with doxorubicin or carboplatin in dogs with osteosarcoma. METHODS: Two percent taurolidine was infused into six healthy dogs (150 mg/kg) over a period of two hours and blood samples were taken periodically. One dog received taurolidine with polyvinylpyrrolidone (PVP) as its carrier and later received PVP-free taurolidine as did all other dogs in this study. Serum taurolidine concentrations were determined using high-performance liquid chromatography (HPLC) online coupled to ESI-MS/MS in the multiple reaction monitoring mode. Subsequently, the same dose of taurolidine was infused to seven dogs with osteosarcoma also treated with doxorubicin or carboplatin. RESULTS: Taurolidine infusion was safe in 6 healthy dogs and there were no significant side effects. Maximum taurolidine serum concentrations ranged between 229 to 646 μM. The dog that received taurolidine with PVP had an immediate allergic reaction but recovered fully after the infusion was stopped. Three additional dogs with osteosarcoma received doxorubicin and taurolidine without PVP. Toxicities included dilated cardiomyopathy, protein-losing nephropathy, renal insufficiency and vasculopathy at the injection site. One dog was switched to carboplatin instead of doxorubicin and an additional 4 dogs with osteosarcoma received taurolidine-carboplatin combination. One incidence of ototoxicity occurred with the taurolidine- carboplatin combination. Bone marrow and gastro-intestinal toxicity did not appear increased with taurolidine over doxorubicin or carboplatin alone. CONCLUSIONS: Taurolidine did not substantially exacerbate bone marrow or gastro-intestinal toxicity however, it is possible that taurolidine increased other toxicities of doxorubicin and carboplatin. Administering taurolidine in combination with 30 mg/m2 doxorubicin in dogs is not recommended but taurolidine in combination with carboplatin (300 mg/m2) appears safe.

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Original publication on PubMed: https://pubmed.ncbi.nlm.nih.gov/24422857/