Effect of α-difluoromethylornithine on Rectal Mucosal levels of polyamines in a randomized, double-blinded trial for colon cancer prevention

Background: Polyamines (e,g., putrescine, spermidine, and spermine) are required for optimal cell growth. Inhibition of polyamine synthesis suppresses carcinogen-induced epithelial cancers, including colon cancer, in animal models, In a short-term phase IIa trial, we determined that low doses of -difluoromethylornithine (DFMO), an inhibitor of ornithine decarboxylase tan enzyme involved in polyamine synthesis), reduced the polyamine content of normal-appearing rectal mucose of subjects with a prior history of resected colon polyps. Zn a follow-up study, We have attempted to determine the lowest dose of DFMO that can suppress the polyamine content of rectal mucosa over a course of a year with no or minimal side effects, Methods: participants were randomly assigned to daily oral treatment With a placebo or one of three doses (0.075, 0.20, or 0.40 g/m(2)) of DFMO, Baseline and serial determinations of polyamine levels ire rectal mucosa and extensive symptom monitoring (including audiometric measurements, since DFMO causes some reversible hearing loss at higher doses) were performed over a 15-month period. Results: DFMO treatment reduced putrescine Bevels in a dose-dependent manner, Following 6 months of treatment, doses of 0.20 and 0.40 g/m2 per day reduced putrescine levels to approximately 34% and 10%, respectively, of those observed in the placebo group, Smaller decreases were seem in spermidine levels and spermidine:spermine ratios. Polyamine levels increased toward baseline values after discontinuation of DFMO. Although there were no statistically significant differences among the dose groups with respect to clinically important shifts in audiometric thresholds and nonaudiologic side effects, statistically significant higher dropout and discontinuation rates were observed in the highest dose group, Conclusions: Polyamine levels in rectal mucosa can he continuously suppressed by daily oral doses of DFMO that produce few or no side effects, a dose of 0.20 g/m(2) can be used safely in chemoprevention phase IIb or single-agent phase III chemoprevention trials.