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Optimization of temporal dose modulation: Comparison of theory and experiment

机译:时间剂量调制的优化:理论与实验的比较

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摘要

Purpose: To compare theoretical predictions and experimental measurements of cell survival after exposure to two different temporally modulated radiation dose patterns that deliver the same dose in the same overall time. Methods: The authors derived an analytic expression for the dose protraction factor G in the Lea-Catcheside formalism for cell survival for triangle and V temporal modulation of dose. These temporal dose patterns were used in experimental clonogenic studies of a melanoma cell line (MM576) and a nonsmall-cell lung cancer line (NCI-H460) that have different alpha, beta, and repair parameters. The overall treatment time and total dose were kept constant. Results: The analytic expressions for G for the two temporal modulations are presented as a function of a single variable, the product of the exposure time, and the repair constant, enabling G to be evaluated for any exposure time and for any cell line. G for the triangle delivery pattern is always the larger. For the MM576 cell line, following a large dose of 6 Gy, a larger survival fraction was found for the V delivery pattern. No difference in survival was observed for lower doses or for the NCI-H460 cell line at any dose. These results are predicted by our theory, using published values of alpha, beta, and repair time within the limits of experimental uncertainty. Conclusions: The study provides evidence to confirm that cell lines having large beta values exhibit a response that is sensitive to the pattern of dose delivery when the delivery time is comparable with the repair time. It is recommended that the dose delivery pattern be considered in hypofractionated treatments.
机译:目的:比较暴露于两种在总时间上相同剂量的不同时间调制辐射剂量模式后细胞存活的理论预测和实验测量结果。方法:作者在Lea-Catcheside形式主义中得出了剂量延长因子G的解析表达式,用于三角形和V时间剂量调节的细胞存活。这些时间剂量模式用于黑色素瘤细胞系(MM576)和非小细胞肺癌系(NCI-H460)具有不同alpha,beta和修复参数的实验性克隆形成研究。总治疗时间和总剂量保持恒定。结果:针对两个时间调制的G解析表达式作为单个变量,暴露时间和修复常数的乘积的函数表示,从而可以针对任何暴露时间和任何细胞系评估G。三角形投放模式的G始终较大。对于MM576细胞系,在6 Gy的大剂量剂量之后,V传递模式的存活率更高。对于低剂量或任何剂量的NCI-H460细胞系,均未观察到存活率差异。这些结果是根据我们的理论预测的,使用了在实验不确定性范围内发布的α,β和修复时间值。结论:该研究提供证据证实当递送时间与修复时间相当时,具有大β值的细胞系表现出对剂量递送模式敏感的反应。建议在超分割治疗中考虑剂量输送方式。

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