In Vivo Combination of Misonidazole and the Chemotherapeutic Agent CCNU
Overview
Authors
Affiliations
The response of intramuscularly growing KHT sarcomas to the chemotherapeutic agent (1-(2-cloroethyl)-3-cyclohexyl-1-nitrosourea (CCNU) alone or simultaneously with the chemical radio-sensitizer misonidazole (MISO) was assessed using either a tumour growth-delay assay or an in vivo-in vitro tumour-excision assay. Median tumour growth delay following the combination of 20 mg/kg CCNU and either 0.5 or 1.0 mg/g MISO was 19.5 and 21.5 days, compared to 10 days for this CCNU dose alone. A similar degree of enhanced tumour response by MISO (factor of approximately 2 in tumour growth delay) was seen in RIF-1 tumours treated with 20 mg/kg CCNU plus 1.0 mg/g MISO. Clonogenic cell-survival studies with KHT sarcomas demonstrated that MISO at doses of 0.25, 0.5 or 1.0 mg/g given simultaneously with a range of CCNU doses produced dose-modifying factors (DMFs) of 1.9, 2.1 and 2.4 respectively. Normal tissue toxicity assessed by an LD50/7 assay led to DMFs of 1.2 and 1.4 for CCNU doses combined with 0.5 and 1.0 mg/g MISO. Thus in this animal tumour model the combination of CCNU and MISO appears to lead to a potential gain by a factor of approximately 1.7.
Formation of DNA adducts and tumor growth delay following intratumoral administration of DTI-015.
Bodell W, Giannini D, Singh S, Pietronigro D, Levin V J Neurooncol. 2003; 62(3):251-8.
PMID: 12777076 DOI: 10.1023/a:1023383717833.
Enhancement of CCNU cytotoxicity by misonidazole: possible therapeutic gain.
Hirst D, Brown J, HAZLEHURST J Br J Cancer. 1982; 46(1):109-16.
PMID: 7201845 PMC: 2011076. DOI: 10.1038/bjc.1982.172.
Workman P, Twentyman P Br J Cancer. 1982; 46(2):249-59.
PMID: 7150475 PMC: 2011106. DOI: 10.1038/bjc.1982.190.
Potentiation of melphalan activity against a murine tumour by nitroimidazole compounds.
SHELDON P, Batten E, Adams G Br J Cancer. 1982; 46(4):525-31.
PMID: 7138761 PMC: 2011202. DOI: 10.1038/bjc.1982.236.
Smith E, Stratford I, Adams G Br J Cancer. 1982; 46(1):117-26.
PMID: 7104191 PMC: 2011057. DOI: 10.1038/bjc.1982.173.