Please use this identifier to cite or link to this item: http://ahro.austin.org.au/austinjspui/handle/1/12929
Title: Blood-brain barrier disruption and methotrexate in the treatment of a readily transplantable intracerebral osteogenic sarcoma of rats.
Authors: Cosolo, W;Christophidis, N
Affiliation: Clinical Pharmacology and Therapeutics Unit, Austin Hospital, Heidelberg, Australia
Issue Date: 1-Dec-1987
Citation: Cancer Research; 47(23): 6225-8
Abstract: An animal model of intracerebral osteogenic sarcoma has been developed to evaluate blood-brain barrier disruption as an adjunct to chemotherapy of intracerebral tumors. Adult Sprague-Dawley rats (n = 225) were inoculated intracerebrally with transplantable, methotrexate sensitive, osteogenic sarcoma cells and 3 days later randomized to receive either no treatment or methotrexate with or without blood-brain barrier disruption using intracarotid mannitol. Methotrexate was administered i.v., i.p., or directly into the carotid artery (i.c.) in doses of 2.5, 10, 20, 50, or 100 mg/kg. Survival was the study's end point. Surgery, anaesthesia, or blood-brain barrier disruption with mannitol did not affect survival. However, there was a significant effect of dose and route of administration of methotrexate on survival. The shortest survival was in rats receiving no treatment in which death occurred reproducibly at 7.6 +/- 0.2 days (n = 29) and the longest survival was 12.7 +/- 0.3 day (p less than 0.001) in those given methotrexate 50 mg/kg i.c. (n = 6). The i.c. route was most effective in prolonging survival followed by i.v. and the least effective was the i.p. route of methotrexate administration. Blood-brain barrier disruption followed by methotrexate (i.v. or i.c.) was deleterious to survival (two-way analysis of variance, p less than 0.003 and p less than 0.011, respectively) and the reduced survival was in part related to early complications such as intratumor hemorrhage or possibly a methotrexate induced encephalopathy. It is concluded that this is a useful model for the study of the chemotherapy of cerebral tumors, that blood-brain barrier disruption did not appear to improve the dose-response curve but resulted in reduced survival. We caution against the use of this procedure in the treatment of cerebral tumor in humans.
Internal ID Number: 3119195
URI: http://ahro.austin.org.au/austinjspui/handle/1/12929
URL: http://www.ncbi.nlm.nih.gov/pubmed/3119195
Type: Journal Article
Subjects: Animals
Blood-Brain Barrier.drug effects
Brain Neoplasms.drug therapy
Carotid Arteries
Injections, Intra-Arterial
Injections, Intraperitoneal
Injections, Intravenous
Mannitol.administration & dosage.pharmacology
Methotrexate.administration & dosage.therapeutic use
Neoplasm Transplantation
Osteosarcoma.drug therapy
Rats
Rats, Inbred Strains
Appears in Collections:Journal articles

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