Daşu Alexandru, Toma-Daşu Iuliana, Fowler Jack F
Department of Radiation Sciences, Umeå University, S-901 85 Umeå, Sweden.
Phys Med Biol. 2003 Feb 7;48(3):387-97. doi: 10.1088/0031-9155/48/3/308.
Linear quadratic (LQ) modelling allows easy comparison of different fractionation schedules in radiotherapy. However, estimating the radiation effect of a single fractionated treatment introduces many questions with respect to the parameters to be used in the modelling process. Several studies have used tumour control probability (TCP) curves in order to derive the values for the LQ parameters that may be used further for the analysis and ranking of treatment plans. Unfortunately, little attention has been paid to the biological relevance of these derived parameters, either for the initial number of cells or their intrinsic radiosensitivity, or both. This paper investigates the relationship between single values for the TCP parameters and the resulting dose-response curve. The results of this modelling study show how clinical observations for the position and steepness of the TCP curve can be explained only by the choice of extreme values for the parameters, if they are single values. These extreme values are in contradiction with experimental observations. This contradiction suggests that single values for the parameters are not likely to explain reasonably the clinical observations and that some distributions of input parameters should be taken into consideration.
线性二次(LQ)模型能够轻松比较放射治疗中不同的分割方案。然而,估计单次分割治疗的放射效应会在建模过程中使用的参数方面引发诸多问题。若干研究使用肿瘤控制概率(TCP)曲线来推导LQ参数的值,这些值可进一步用于分析和排列治疗计划。遗憾的是,对于这些推导参数的生物学相关性,无论是关于初始细胞数量还是其内在放射敏感性,或者两者,都很少有人关注。本文研究了TCP参数的单个值与所得剂量反应曲线之间的关系。该建模研究的结果表明,如果TCP曲线参数是单个值,那么只有通过选择这些参数的极值才能解释临床观察到的TCP曲线位置和斜率情况。这些极值与实验观察结果相矛盾。这种矛盾表明,参数的单个值不太可能合理地解释临床观察结果,应该考虑输入参数的一些分布情况。