Au J L, Rustum Y M, Slocum H K
College of Pharmacy, Ohio State University, Columbus 43210.
Cancer Drug Deliv. 1987;4(3):137-44. doi: 10.1089/cdd.1987.4.137.
The antitumor activity and toxicity of 5-fluorouracil (FUra) and 5'-deoxy-5-fluorouridine (dFUR) were compared in female Fischer rats bearing transplanted dimethylhydrazine-induced colon tumors. The therapeutic effects of FUra and dFUR were not affected by the initial tumor size, but were dependent on the dose and duration of treatment. The maximal response rate of 80-90% cures was obtained with 7-day infusions of 35 mg-kg-1-day-1 FUra or 500 mg-kg-1-day-1 dFUR. The host toxicity of FUra and dFUR in tumor-bearing or normal rats included gastrointestinal and central nervous system disturbances. Toxicity related death was preceded by a greater than 20% animal weight loss and other signs of gastrointestinal disturbances. The maximal therapeutic dose of FUra was identical to the toxic dose which caused 40% death in normal rats. By contrast, the maximal therapeutic dose of dFUR did not cause toxic death, and the threshold lethal dose of dFUR was 40% higher than the maximally therapeutic dose, indicating a better therapeutic index for dFUR in this rat tumor.
在携带二甲基肼诱导的移植性结肠肿瘤的雌性Fischer大鼠中,比较了5-氟尿嘧啶(FUra)和5'-脱氧-5-氟尿苷(dFUR)的抗肿瘤活性和毒性。FUra和dFUR的治疗效果不受初始肿瘤大小的影响,但取决于治疗剂量和持续时间。连续7天输注35mg·kg⁻¹·d⁻¹的FUra或500mg·kg⁻¹·d⁻¹的dFUR可获得80-90%治愈率的最大反应率。FUra和dFUR对荷瘤或正常大鼠的宿主毒性包括胃肠道和中枢神经系统紊乱。毒性相关死亡之前动物体重减轻超过20%以及出现其他胃肠道紊乱迹象。FUra的最大治疗剂量与导致正常大鼠40%死亡的毒性剂量相同。相比之下,dFUR的最大治疗剂量未导致毒性死亡,且dFUR的阈致死剂量比最大治疗剂量高40%,表明dFUR在该大鼠肿瘤模型中具有更好的治疗指数。