Kondo H, Kanzawa F, Nishio K, Saito S, Saijo N
Pharmacology Division, National Cancer Center Research Institute, Tokyo.
Jpn J Cancer Res. 1994 Oct;85(10):1050-6. doi: 10.1111/j.1349-7006.1994.tb02905.x.
The effects of cisplatin (CDDP) and etoposide (ETP) in combination were evaluated in vitro and in vivo using small cell lung cancer cell lines. The combination effects in vitro were investigated using isobologram analysis. Used together, CDDP and ETP showed a synergistic effect against cell growth on only 1 cell line (SBC-3), additive effects on 6 (SBC-2, SBC-5, Lu130, Lu134AH, Lu135T and H69) and an antagonistic effect on 1 (SBC-1). In the in vivo experiment, nude mice were inoculated with SBC-1, SBC-3 and SBC-5 cells. Two or 5 mg/kg CDDP and 10 or 30 mg/kg ETP were administered intraperitoneally alone and simultaneously in combination to nude mice. The in vivo effects of the combination were determined by comparing the observed growth ratio in mice treated with the combination with the expected value of this ratio calculated based on the assumption that the effects of the drugs were simply additive. According to this definition, synergistic effects were observed against all 3 tumors. Thus, the in vivo and in vitro effects differed. The toxicity of the combination therapy, which was analyzed by estimating the body weight change of mice, was no higher than that of CDDP or ETP alone. These results suggest that the excellent clinical effects of CDDP and ETP combination therapy may be attributable not to drug interaction at the cellular level but to the feasibility of combined use of them at full doses without overlapping side effects.
使用小细胞肺癌细胞系在体外和体内评估了顺铂(CDDP)和依托泊苷(ETP)联合使用的效果。使用等效线图分析研究了体外联合效果。CDDP和ETP联合使用时,仅对1种细胞系(SBC - 3)的细胞生长显示出协同作用,对6种细胞系(SBC - 2、SBC - 5、Lu130、Lu134AH、Lu135T和H69)显示出相加作用,对1种细胞系(SBC - 1)显示出拮抗作用。在体内实验中,将SBC - 1、SBC - 3和SBC - 5细胞接种到裸鼠体内。将2或5mg/kg的CDDP和10或30mg/kg的ETP单独及联合同时腹腔注射给裸鼠。通过比较联合治疗小鼠的观察生长率与基于药物作用简单相加假设计算出的该比率预期值,来确定联合用药的体内效果。根据此定义,对所有3种肿瘤均观察到协同作用。因此,体内和体外效果不同。通过估计小鼠体重变化分析的联合治疗毒性不高于单独使用CDDP或ETP的毒性。这些结果表明,CDDP和ETP联合治疗的优异临床效果可能并非归因于细胞水平的药物相互作用,而是归因于它们以全剂量联合使用且无重叠副作用的可行性。