Feola J, Maruyama Y
Cancer Treat Rep. 1979 Aug;63(8):1409-12.
C57BL mice carrying the syngeneic advanced LSA ascites lymphoma initiated with a 10(6)-cell LSA inoculum were treated with four combinations of BCNU and/or chlorozotocin (CLZ) on Days 5 and 6 after tumor inoculation. The percentage of mice surviving greater than or equal to 60 days was greater than 80% for all four combinations. Surviving mice were then challenged with live LSA cells beginning with 100 cells and increasing the inoculum by factors of 10 every 3 weeks until a 10(7)-cell inoculum level was reached. The latter dose was repeated four times. A marked difference in resistance to tumor challenge was observed for the various groups. Surviving tumor-resistant mice at the end of the experiment, classified by original treatment, were as follows: BCNU-BCNU, 86.7%; CLZ-BCNU, 56.3%; BCNU-CLZ, 23.5% and CLZ-CLZ, 0. Various hypotheses are presented which might explain these differences.
用10⁶个LSA接种物引发同基因晚期LSA腹水淋巴瘤的C57BL小鼠,在肿瘤接种后第5天和第6天用卡莫司汀(BCNU)和/或氯脲霉素(CLZ)的四种组合进行治疗。所有四种组合中存活超过或等于60天的小鼠百分比均大于80%。然后,从100个活LSA细胞开始,每隔3周将接种物增加10倍,直至达到10⁷个细胞的接种水平,对存活小鼠进行活LSA细胞攻击。后一剂量重复四次。观察到不同组对肿瘤攻击的抗性存在显著差异。实验结束时,按原始治疗分类的存活的抗瘤小鼠如下:BCNU-BCNU组,86.7%;CLZ-BCNU组,56.3%;BCNU-CLZ组,23.5%;CLZ-CLZ组,0。提出了各种可能解释这些差异的假说。