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低于2Gy时,随着分次剂量降低,大鼠脊髓耐受性增加缺乏证据。

Lack of evidence for increased tolerance of rat spinal cord with decreasing fraction doses below 2 Gy.

作者信息

Ang K K, van der Kogel A J, van der Schueren E

出版信息

Int J Radiat Oncol Biol Phys. 1985 Jan;11(1):105-10. doi: 10.1016/0360-3016(85)90368-2.

Abstract

The radiation tolerance of the spinal cord, both in man and in rats, has been shown to depend strongly on the size of the dose per fraction. With fraction doses down to about 2 Gy, the spinal cord tolerance can be predicted by a modified Ellis formula: D approximately N0.43. More recently alternative isoeffect formulas were based on the linear-quadratic (LQ) model of cell survival where the effect of dose fractionation is characterized by the ratio alpha/beta which varies from tissue to tissue. For the spinal cord, as well as for other late responding tissues, the ratio alpha/beta is small, in contrast to most acutely responding tissues. Both the Ellis-type formula, and to a lesser extent the LQ-model, predict a continuously increasing tolerance dose with decreasing fraction size. From the LQ model, the concept of "flexure dose" has been derived, which proposes the limit of effective fractionation to be about 0.1 alpha/beta. At this dose per fraction no significant further gain in tolerance would be detected. From previous experiments on the rat cervical spinal cord with doses per fraction down to about 2 Gy, the ratio alpha/beta was determined to be 1.7 Gy, and the LQ-model would predict a rise in tolerance with a reduction in fraction size to far below 2 Gy. Based on these predictions clinical studies have been initiated assuming a significantly increased tolerance by reduction of fraction size to about 1 Gy. However, in the present experiments no evidence was found for such an increase in tolerance with fraction sizes below 2 Gy.

摘要

已表明,人类和大鼠脊髓的辐射耐受性在很大程度上取决于每次分割剂量的大小。当分割剂量低至约2 Gy时,脊髓耐受性可通过修正的埃利斯公式预测:D≈N0.43。最近,替代的等效效应公式基于细胞存活的线性二次(LQ)模型,其中剂量分割的效应由α/β比值表征,该比值因组织而异。与大多数急性反应组织相比,脊髓以及其他晚期反应组织的α/β比值较小。埃利斯型公式以及在较小程度上的LQ模型,均预测随着分割大小减小,耐受剂量会持续增加。从LQ模型中推导出了“转折剂量”的概念,该概念提出有效分割的极限约为0.1α/β。在这个每次分割剂量下,不会检测到耐受性有显著进一步提高。根据先前对大鼠颈髓进行的每次分割剂量低至约2 Gy的实验,确定α/β比值为1.7 Gy,LQ模型预测随着分割大小减小至远低于2 Gy,耐受性会升高。基于这些预测,已启动临床研究,假设通过将分割大小减小至约1 Gy可显著提高耐受性。然而,在目前的实验中,未发现分割大小低于2 Gy时耐受性增加的证据。

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