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Serum concentration and safety of intravenous drip versus subcutaneous administration of carboplatin in dogs
Carboplatin is used to treat certain cancers in dogs and cats and is routinely administered via intravenous drip (IVD). Subcutaneous (SC) administration has also been described. However, the toxicity, serum concentrations, and area under blood concentration-time curves (AUCs) of SC carboplatin are u...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
The Japanese Society of Veterinary Science
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8182319/ https://www.ncbi.nlm.nih.gov/pubmed/33716231 http://dx.doi.org/10.1292/jvms.20-0653 |
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author | IWANO, Masataka SADAHIRO, Kohei MARUO, Takuya KAWARAI, Shinpei KAYANUMA, Hideki ORITO, Kensuke |
author_facet | IWANO, Masataka SADAHIRO, Kohei MARUO, Takuya KAWARAI, Shinpei KAYANUMA, Hideki ORITO, Kensuke |
author_sort | IWANO, Masataka |
collection | PubMed |
description | Carboplatin is used to treat certain cancers in dogs and cats and is routinely administered via intravenous drip (IVD). Subcutaneous (SC) administration has also been described. However, the toxicity, serum concentrations, and area under blood concentration-time curves (AUCs) of SC carboplatin are unknown. This study aimed to compare serum carboplatin concentrations in dogs after SC and IVD and to monitor any adverse events. In this crossover study, five dogs received SC or IV carboplatin (300 mg/m(2)). After a minimum of 3 weeks, each dog received the other treatment. No gross skin toxicity or abnormal clinical signs were observed in any of the dogs. Blood test abnormalities were detected in most dogs. Decreased neutrophil and platelet counts, and increased C-reactive protein (CRP) levels were found. There was no significant difference in the neutropenia, thrombocytopenia, and CRP scores between the groups. Systemic toxicities of SC carboplatin were comparable to those of IVD carboplatin. The time to maximum carboplatin concentration after SC was longer than that after IVD (P<0.001). SC carboplatin remained in the serum longer than IVD carboplatin (P=0.008). The AUC of SC was less than that of IVD (P=0.002). The AUC and time taken to reach the maximum concentration of SC carboplatin were lower than those of IVD carboplatin. This study suggests that SC carboplatin may be an efficacious option for the treatment of tumors in dogs, particularly where IVD administration is challenging. |
format | Online Article Text |
id | pubmed-8182319 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | The Japanese Society of Veterinary Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-81823192021-06-09 Serum concentration and safety of intravenous drip versus subcutaneous administration of carboplatin in dogs IWANO, Masataka SADAHIRO, Kohei MARUO, Takuya KAWARAI, Shinpei KAYANUMA, Hideki ORITO, Kensuke J Vet Med Sci Internal Medicine Carboplatin is used to treat certain cancers in dogs and cats and is routinely administered via intravenous drip (IVD). Subcutaneous (SC) administration has also been described. However, the toxicity, serum concentrations, and area under blood concentration-time curves (AUCs) of SC carboplatin are unknown. This study aimed to compare serum carboplatin concentrations in dogs after SC and IVD and to monitor any adverse events. In this crossover study, five dogs received SC or IV carboplatin (300 mg/m(2)). After a minimum of 3 weeks, each dog received the other treatment. No gross skin toxicity or abnormal clinical signs were observed in any of the dogs. Blood test abnormalities were detected in most dogs. Decreased neutrophil and platelet counts, and increased C-reactive protein (CRP) levels were found. There was no significant difference in the neutropenia, thrombocytopenia, and CRP scores between the groups. Systemic toxicities of SC carboplatin were comparable to those of IVD carboplatin. The time to maximum carboplatin concentration after SC was longer than that after IVD (P<0.001). SC carboplatin remained in the serum longer than IVD carboplatin (P=0.008). The AUC of SC was less than that of IVD (P=0.002). The AUC and time taken to reach the maximum concentration of SC carboplatin were lower than those of IVD carboplatin. This study suggests that SC carboplatin may be an efficacious option for the treatment of tumors in dogs, particularly where IVD administration is challenging. The Japanese Society of Veterinary Science 2021-03-15 2021-05 /pmc/articles/PMC8182319/ /pubmed/33716231 http://dx.doi.org/10.1292/jvms.20-0653 Text en ©2021 The Japanese Society of Veterinary Science https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution Non-Commercial No Derivatives (by-nc-nd) License. (CC-BY-NC-ND 4.0: https://creativecommons.org/licenses/by-nc-nd/4.0/) |
spellingShingle | Internal Medicine IWANO, Masataka SADAHIRO, Kohei MARUO, Takuya KAWARAI, Shinpei KAYANUMA, Hideki ORITO, Kensuke Serum concentration and safety of intravenous drip versus subcutaneous administration of carboplatin in dogs |
title | Serum concentration and safety of intravenous drip versus subcutaneous administration of carboplatin in dogs |
title_full | Serum concentration and safety of intravenous drip versus subcutaneous administration of carboplatin in dogs |
title_fullStr | Serum concentration and safety of intravenous drip versus subcutaneous administration of carboplatin in dogs |
title_full_unstemmed | Serum concentration and safety of intravenous drip versus subcutaneous administration of carboplatin in dogs |
title_short | Serum concentration and safety of intravenous drip versus subcutaneous administration of carboplatin in dogs |
title_sort | serum concentration and safety of intravenous drip versus subcutaneous administration of carboplatin in dogs |
topic | Internal Medicine |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8182319/ https://www.ncbi.nlm.nih.gov/pubmed/33716231 http://dx.doi.org/10.1292/jvms.20-0653 |
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