Abstract

The combination of nicotinamide and carbogen breathing is awaiting clinical evaluation as a strategy to overcome tumour hypoxia and thus enhance radiation response. We have continued our evaluation of this approach in the murine SCCVII tumour with the aim of determining the importance of nicotinamide dose and the pre-irradiation breathing time (PIBT) for carbogen. For carbogen breathing alone maximal enhancement of radiation response was observed with PIBT's of between 5 and 30 min. When nicotinamide (1,000 mg kg-1 IP) was administered 60 min prior to irradiation little or no variation in radiation response was observed for all the PIBT's examined (5-90 min). Indeed at all PIBT's the cell survival obtained for the carbogen nicotinamide and radiation combination was indistinguishable from that expected for a fully aerobic response. For PIBT's of 15 and 60 min we examined the influence of nicotinamide doses between 50 and 1,000 mg kg-1. Significant radiosensitizing effects were observed for all nicotinamide doses tested above 50 mg kg-1. Moreover for doses of 250 mg kg-1 and above the cell survival data was consistent with that expected for a fully aerobic response. No additional benefit accrued from raising the nicotinamide dose above 250 mg kg-1. These results indicate that significant radiosensitization may be expected even with clinically achievable nicotinamide doses when it is combined with carbogen breathing. Furthermore, the use of nicotinamide may reduce the critical importance of PIBT on the radiosensitization observed with carbogen.

Highlights

  • In order to study the effect of a strategy which reduces tumour hypoxia we chose a radiation dose of 14 Gy

  • The results indicate that nicotinamide alone enhanced radiation response at all doses above 50 mg kg-'

  • We have previously shown in the SCCVII and KHT tumours that nicotinamide, when combined with carbogen and a perfluorochemical emulsion, can enhance the response to single doses of X-rays

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Summary

Methods

Mice and tumourSCCVII tumours were obtained by injecting 106 tumour cells subcutaneously over the sacral region of the back in 6-9 week old female C3H/He mice (Charles River Inc., Quebec, Canada). The drug was dissolved in sterile phosphate-buffered saline (PBS) and administered intraperitoneally (i.p.) in a volume of 0.5 ml 25 g-'

Results
Discussion
Conclusion
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