Siemann D W
Br J Cancer Suppl. 1980 Apr;4:294-8.
Isoeffect analysis of complete dose response curves can be used to study the interaction of agents in combined modality protocols. When such an analysis is applied to data from in vivo tumour model systems, the effects of the agents on factors such as tumour vasculature, growth or reoxygenation pattern also need to be considered. In this study the change in tumour size, which can occur during a long time-interval between agents, was used as an example of a factor which may influence the position of data points on an isoeffect plot. Assays of in vivo tumour growth delay and in vitro clonogenic survival were performed to demonstrate that the radiation response curves of EMT-6/Ro tumours were size dependent. These curves were used to illustrate that data points obtained from a combined modality treatment may fall outside of the envelope of additivity of an isoeffect plot, as a direct consequence of tumour growth. This finding indicates that it may not be possible to interpret the results from isoeffect analyses of in vivo data on the basis of cellular interactions between agents, and suggests that instead isoeffect analyses be applied primarily to assess the overall response of the tumour system.
完整剂量反应曲线的等效效应分析可用于研究联合治疗方案中药物的相互作用。当将这种分析应用于体内肿瘤模型系统的数据时,还需要考虑药物对肿瘤血管生成、生长或再氧合模式等因素的影响。在本研究中,以药物之间较长时间间隔内可能发生的肿瘤大小变化为例,说明其可能影响等效效应图上数据点的位置。进行了体内肿瘤生长延迟测定和体外克隆形成存活测定,以证明EMT-6/Ro肿瘤的放射反应曲线与肿瘤大小有关。这些曲线用于说明,联合治疗获得的数据点可能落在等效效应图的相加性范围之外,这是肿瘤生长的直接结果。这一发现表明,基于药物之间的细胞相互作用来解释体内数据的等效效应分析结果可能是不可能的,并建议等效效应分析主要应用于评估肿瘤系统的整体反应。