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用于三维治疗计划的放射毒性模型。第1部分:理论基础。

Radiotoxic model for three-dimensional treatment planning. Part 1: Theoretical basis.

作者信息

Caudry M, Causse N, Trouette R, Récaldini L, Maire J P, Demeaux H

机构信息

Service de Radiothérapie, Hôpital Saint-André, Bordeaux, France.

出版信息

Int J Radiat Oncol Biol Phys. 1993 Apr 2;25(5):907-19. doi: 10.1016/0360-3016(93)90322-m.

Abstract

Since recent treatment planning systems calculate volumetric dose distribution, an objective evaluation of potential toxicity in the main critical organs may be helpful in treatment optimization. Modeling the toxicity of radiotherapy must at least account for: (a) specific risks in every critical organ; (b) total dose and dose per fraction; (c) partial irradiation of critical organs; (d) heterogeneous dose distribution. The Radiation Damage Factor formula is aimed at estimating the delayed toxicity of a given treatment plan on every critical organ concerned. The formulation uses a double exponential function: RDF = 100 e-Ke-(a+bd)DVc, where: D is the total dose, and d the dose per fraction; a and b are coefficients representing the radiosensitivity of the critical organ, according to the linear-quadratic model, with a/b = alpha/beta. K represents the theoretical critical unit content of the organ, these critical units being groups of functionally related stem cells. The avoidance of a complication depends on the ability of surviving critical units to preserve organ function. V is the ratio:irradiated volume/total volume of the organ. Exponent c accounts for tissue organization: c is equal to or near 1 in "parallel organs" like the liver or the lung, where localized hot spots are tolerated; c is lower in "series organs" like the spinal cord where hot spots, even in a small portion, are dangerous. Heterogeneous irradiation, summarized by dose cumulative-volume histograms, is accounted for by calculating step by step the dose D' considered as having an equivalent effect when given in the largest irradiated volume ratio. Preliminary calibration of the RDF formula is attempted for radiation myelitis and radiation hepatitis.

摘要

由于近期的治疗计划系统能够计算体积剂量分布,因此对主要关键器官潜在毒性进行客观评估可能有助于优化治疗。放疗毒性建模至少必须考虑:(a) 每个关键器官的特定风险;(b) 总剂量和分次剂量;(c) 关键器官的部分照射;(d) 不均匀剂量分布。辐射损伤因子公式旨在估计给定治疗计划对每个相关关键器官的迟发性毒性。该公式使用双指数函数:RDF = 100 e-Ke-(a+bd)DVc,其中:D为总剂量,d为分次剂量;a和b是根据线性二次模型表示关键器官放射敏感性的系数,a/b = α/β。K代表器官的理论关键单位含量,这些关键单位是功能相关干细胞群。并发症的避免取决于存活关键单位维持器官功能的能力。V是比值:照射体积/器官总体积。指数c考虑组织结构:在肝脏或肺等“平行器官”中,c等于或接近1,其中局部热点是可耐受的;在脊髓等“串联器官”中,c较低,其中即使一小部分热点也是危险的。由剂量累积体积直方图总结的不均匀照射,通过逐步计算在最大照射体积比下给予时被视为具有等效效应的剂量D'来考虑。尝试对辐射性脊髓炎和放射性肝炎进行RDF公式的初步校准。

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