High mitomycin C concentration in tumour tissue can be achieved by isolated liver perfusion in rats View Full Text


Ontology type: schema:ScholarlyArticle     


Article Info

DATE

1991-03

AUTHORS

Andreas Marinelli, Dirk H. A. Pons, Jacqueline A. C. Vreeken, Suresh K. Nagesser, Peter J. K. Kuppen, Ubbo R. Tjaden, Cornelis J. H. van de Velde

ABSTRACT

To enable the treatment of hepatic metastasis with higher, theoretically more effective, doses of systemically toxic anticancer drugs, an isolated liver perfusion (ILP) technique was developed in WAG/Ola rats. First, in a toxicity study the maximally tolerated dose (MTD) of mitomycin C (MMC) was determined for a 25-min ILP and for hepatic artery infusion (HAI) after the administration of a bolus dose. The MTD in the ILP setting (4.8 mg/kg) was 4 times that using HAI (1.2 mg/kg). Subsequently, in a rat colorectal hepatic-metastasis model, concentrations of MMC in tumour, liver, plasma and perfusate were measured during a 25-min ILP to investigate the expected pharmacokinetic advantage of ILP. The mean plasma level determined after ILP (1.2 as well as 4.8 mg/kg MMC) was significantly lower (P less than 0.001) than that obtained following HAI. This may explain both the absence of severe systemic toxicity and the higher MTD in ILP-treated groups. No significant difference in mean tumour and liver tissue concentrations of MMC were found when the groups treated with 1.2 mg/kg drug via HAI vs ILP were compared. The mean MMC concentration in tumour tissue was significantly higher (almost 5 times; P less than 0.05) in rats treated by ILP with the MTD (4.8 mg/kg) than in those treated via HAI with the MTD (1.2 mg/kg). ILP of MMC can be safely performed using a dose 4 times higher than the MTD in the HAI setting, leading to an almost 5-fold concentration of MMC in hepatic metastasis. ILP of MMC may therefore represent a promising therapy for metastasis confined to the liver. More... »

PAGES

109-114

References to SciGraph publications

Identifiers

URI

http://scigraph.springernature.com/pub.10.1007/bf00689698

DOI

http://dx.doi.org/10.1007/bf00689698

DIMENSIONS

https://app.dimensions.ai/details/publication/pub.1013813775

PUBMED

https://www.ncbi.nlm.nih.gov/pubmed/1905590


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