The effect of
adenosine dialdehyde (AD) on in situ
tumor growth and host survival was evaluated in the C1300 murine
neuroblastoma tumor model prepared by implantation of murine
neuroblastoma cells into A/J mice. AD was administered s.c. by one of the following treatment regimens: regimen A, single daily dose for 5 days;
regimen B, minipump infusion for 7 days; regimen C, minipump infusion for 14 days; regimen D, minipump infusion for two 7-day periods interspersed by a 7-day
drug free interval. AD doses of 1.5 to 2.5 mg/kg/day infused over a 7-day period (
regimen B) significantly increased the mean life span of
tumor bearing mice from 20.9 +/- 1.2 days (mean +/- 2 SEM) in diluent treated controls to 35.3 +/- 2.1 days in AD treated animals (mean increase +/- 2 SEM: 69 +/- 10%; P less than 0.0001). This treatment regimen also produced a 56 +/- 13% decrease in
tumor diameter (P less than 0.0001). Administration of AD for two 7-day infusion periods, interspersed by a 7-day
drug free interval (regimen D), increased mean life span 80% (controls, 21.3 +/- 4.4 days; AD treated 38.4 +/- 5.6 days; P less than 0.0005). Hematopoietic toxicity was not observed when doses between 2 and 3 mg/kg/day of AD were infused for 7 days (
regimen B). These data suggest that steady state infusions of AD can significantly suppress murine
neuroblastoma tumor growth with little systemic toxicity. In contrast, single daily
injections of AD were ineffective and toxic to the
tumor bearing host.