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Pharmacokinetic study and evaluation of the safety of taurolidine for dogs with osteosarcoma

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...

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Autores principales: Marley, Kevin, Helfand, Stuart C, Simpson, Jennifer, Mata, John E, Tracewell, William G, Brownlee, Lisa, Bracha, Shay, Séguin, Bernard
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3852505/
https://www.ncbi.nlm.nih.gov/pubmed/24422857
http://dx.doi.org/10.1186/1756-9966-32-74
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author Marley, Kevin
Helfand, Stuart C
Simpson, Jennifer
Mata, John E
Tracewell, William G
Brownlee, Lisa
Bracha, Shay
Séguin, Bernard
author_facet Marley, Kevin
Helfand, Stuart C
Simpson, Jennifer
Mata, John E
Tracewell, William G
Brownlee, Lisa
Bracha, Shay
Séguin, Bernard
author_sort Marley, Kevin
collection PubMed
description 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/m(2) doxorubicin in dogs is not recommended but taurolidine in combination with carboplatin (300 mg/m(2)) appears safe.
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spelling pubmed-38525052013-12-06 Pharmacokinetic study and evaluation of the safety of taurolidine for dogs with osteosarcoma Marley, Kevin Helfand, Stuart C Simpson, Jennifer Mata, John E Tracewell, William G Brownlee, Lisa Bracha, Shay Séguin, Bernard J Exp Clin Cancer Res Research 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/m(2) doxorubicin in dogs is not recommended but taurolidine in combination with carboplatin (300 mg/m(2)) appears safe. BioMed Central 2013-10-11 /pmc/articles/PMC3852505/ /pubmed/24422857 http://dx.doi.org/10.1186/1756-9966-32-74 Text en Copyright © 2013 Marley et al.; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research
Marley, Kevin
Helfand, Stuart C
Simpson, Jennifer
Mata, John E
Tracewell, William G
Brownlee, Lisa
Bracha, Shay
Séguin, Bernard
Pharmacokinetic study and evaluation of the safety of taurolidine for dogs with osteosarcoma
title Pharmacokinetic study and evaluation of the safety of taurolidine for dogs with osteosarcoma
title_full Pharmacokinetic study and evaluation of the safety of taurolidine for dogs with osteosarcoma
title_fullStr Pharmacokinetic study and evaluation of the safety of taurolidine for dogs with osteosarcoma
title_full_unstemmed Pharmacokinetic study and evaluation of the safety of taurolidine for dogs with osteosarcoma
title_short Pharmacokinetic study and evaluation of the safety of taurolidine for dogs with osteosarcoma
title_sort pharmacokinetic study and evaluation of the safety of taurolidine for dogs with osteosarcoma
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3852505/
https://www.ncbi.nlm.nih.gov/pubmed/24422857
http://dx.doi.org/10.1186/1756-9966-32-74
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