Garcia L M, Leblanc J, Wilkins D, Raaphorst G P
Department of Physics, Carleton University, Ottawa, K1S5B6, Canada.
Phys Med Biol. 2006 Jun 7;51(11):2813-23. doi: 10.1088/0031-9155/51/11/009. Epub 2006 May 17.
Survival curve behaviour and degree of correspondence between the linear-quadratic (LQ) model and experimental data in an extensive dose range for high dose rates were analysed. Detailed clonogenic assays with irradiation given in 0.5 Gy increments and a total dose range varying from 10.5 to 16 Gy were performed. The cell lines investigated were: CHOAA8 (Chinese hamster fibroblast cells), U373MG (human glioblastoma cells), CP3 and DU145 (human prostate carcinoma cell lines). The analyses were based on chi2-statistics and Monte Carlo simulation of the experiments. A decline of LQ fit quality at very low doses (<2 Gy) is observed. This result can be explained by the hypersensitive effect observed in CHOAA8, U373MG and DU145 data and an adaptive-type response in the CP3 cell line. A clear improvement of the fit is discerned by removing the low dose data points. The fit worsening at high doses also shows that LQ cannot explain this region. This shows that the LQ model fits better the middle dose region of the survival curve. The analysis conducted in our study reveals a dose dependency of the LQ fit in different cell lines.
分析了高剂量率下广泛剂量范围内线性二次(LQ)模型与实验数据之间的生存曲线行为和对应程度。进行了详细的克隆形成试验,以0.5 Gy的增量给予辐照,总剂量范围为10.5至16 Gy。所研究的细胞系包括:CHOAA8(中国仓鼠成纤维细胞)、U373MG(人胶质母细胞瘤细胞)、CP3和DU145(人前列腺癌细胞系)。分析基于实验的卡方统计和蒙特卡罗模拟。观察到在非常低的剂量(<2 Gy)下LQ拟合质量下降。这一结果可以通过在CHOAA8、U373MG和DU145数据中观察到的超敏效应以及CP3细胞系中的适应性反应来解释。通过去除低剂量数据点可以明显看出拟合得到改善。高剂量下拟合变差也表明LQ无法解释该区域。这表明LQ模型更适合生存曲线的中间剂量区域。我们研究中进行的分析揭示了不同细胞系中LQ拟合的剂量依赖性。