Haddock M G, Ames M M, Bonner J A
Division of Radiation Oncology, Mayo Clinic Rochester, Minnesota 55905, USA.
Mayo Clin Proc. 1995 Nov;70(11):1053-60. doi: 10.4065/70.11.1053.
To compare the interactions of two topoisomerase II inhibitors, etoposide and idarubicin, with irradiation.
Two mathematical modeling systems were used to assess the interactions.
Hamster lung fibroblast cells (V79) were exposed to etoposide or idarubicin for 24 hours before or immediately after irradiation. Post radiation treatment with etoposide or idarubicin resulted in radiosensitization, as demonstrated by a decrease in the mean inactivation dose. Exposure to either drug before irradiation resulted in no radiosensitization. The first mathematical modeling system used was isobologram analysis. This analysis revealed a synergistic interaction if etoposide exposure followed irradiation. The interaction from the combination of irradiation and preradiation etoposide was within the envelope of addivity. Irradiation and postradiation idarubicin exposure also resulted in an interaction within the envelope of addivity, whereas preradiation idarubicin exposure resulted in a slightly less than additive interaction. Next, analyses were performed by the median effect principle. Synergistic interactions were demonstrated for combinations of etoposide and irradiation as well as idarubicin and irradiation. Synergistic interactions were more likely when drug exposure (either idarubicin or etoposide) followed irradiation. Experiments at various ratios of radiation dose to drug concentration showed that the likelihood of a synergistic interaction increased as the drug concentration increased relative to the radiation dose.
The interaction of irradiation with topoisomerase II-reactive agents should be further explored in human tumor cell lines.
比较两种拓扑异构酶II抑制剂依托泊苷和伊达比星与辐射的相互作用。
使用两种数学建模系统来评估相互作用。
仓鼠肺成纤维细胞(V79)在辐射前或辐射后立即暴露于依托泊苷或伊达比星24小时。辐射后用依托泊苷或伊达比星治疗导致放射增敏,这通过平均失活剂量的降低得到证明。在辐射前暴露于任何一种药物均未导致放射增敏。使用的第一个数学建模系统是等效线图分析。该分析表明,如果在辐射后暴露于依托泊苷,则存在协同相互作用。辐射与辐射前依托泊苷联合使用的相互作用在相加范围内。辐射与辐射后伊达比星暴露也导致在相加范围内的相互作用,而辐射前伊达比星暴露导致略小于相加的相互作用。接下来,通过中位效应原理进行分析。依托泊苷与辐射以及伊达比星与辐射的组合均显示出协同相互作用。当药物暴露(伊达比星或依托泊苷)在辐射后时,协同相互作用更有可能发生。在不同辐射剂量与药物浓度比下进行的实验表明,随着药物浓度相对于辐射剂量的增加,协同相互作用的可能性增加。
应在人肿瘤细胞系中进一步探索辐射与拓扑异构酶II反应性药物的相互作用。