Wong C S, Hao Y, Hill R P
Department of Radiation Oncology, Princess Margaret Hospital, Ontario Cancer Institute, Toronto, Canada.
Radiother Oncol. 1995 Jul;36(1):44-9. doi: 10.1016/0167-8140(95)01558-x.
Our previous work with rat spinal cord demonstrated that the linear quadratic (LQ) model based on data for large fraction sizes (alpha/beta of 2.4 Gy) failed to predict isoeffective doses between 1 and 2 Gy per fraction, and under-estimated the sparing effect of small doses per fraction given once daily. In contrast, data from mouse skin and kidney, and recent in vitro results revealed a paradoxical increase in radiosensitivity at below 1 Gy per fraction. To assess whether enhanced radiosensitivity is present in the spinal cord below 1 Gy per fraction, the rat spinal cord (C2-T2) was irradiated initially with three daily doses of 10.25 Gy (top-up doses representing 90% of tolerance), followed by graded single doses or fractionated doses in 1.5, 1.0, 0.8, 0.6 or 0.4 Gy fractions given once daily. To limit the overall treatment time to < or = 8 weeks, a small number of the 0.6- and 0.4-Gy fractions were given twice daily with an interfraction interval of 16 h. The end-point was forelimb paralysis secondary to white matter necrosis, confirmed histologically. The ED50 values, excluding the top-up doses, were 5.8, 10.6, 14.8, 15.2, 15.9 and 19.1 Gy for a single dose and doses in 1.5-, 1.0-, 0.8-, 0.6- and 0.4-Gy fractions, respectively. The data gave an alpha/beta of 2.1 Gy (95% CI, 1.4, 2.7 Gy). Pooling the data separately, the alpha/beta value was 2.3 Gy (95% CI, 0.82, 3.7 Gy) for fraction sizes > or = 1 Gy, and 1.2 Gy (95% CI, 0.16, 2.3 Gy) for the 0.8-, 0.6- and 0.4-Gy experiments.(ABSTRACT TRUNCATED AT 250 WORDS)
我们之前对大鼠脊髓的研究表明,基于大分割剂量数据(α/β为2.4 Gy)的线性二次(LQ)模型无法预测每次分割剂量在1至2 Gy之间的等效剂量,并且低估了每日一次给予的小分割剂量的保护效应。相比之下,来自小鼠皮肤和肾脏的数据以及近期的体外研究结果显示,在每次分割剂量低于1 Gy时,放射敏感性出现了反常增加。为了评估在每次分割剂量低于1 Gy时脊髓是否存在放射敏感性增强的情况,首先对大鼠脊髓(C2 - T2)给予每日三次、每次10.25 Gy的剂量(补充剂量,相当于耐受剂量的90%),随后每日一次给予1.5、1.0、0.8、0.6或0.4 Gy分割的分级单次剂量或分次剂量。为了将总治疗时间限制在≤8周,少数0.6和0.4 Gy分割剂量每日给予两次,两次分割间隔为16小时。终点指标是继发于白质坏死的前肢麻痹,通过组织学检查确认。不包括补充剂量时,单次剂量以及1.5、1.0、0.8、0.6和0.4 Gy分割剂量的ED50值分别为5.8、10.6、14.8、15.2、15.9和19.1 Gy。数据得出α/β为2.1 Gy(95%置信区间,1.4,2.7 Gy)。分别汇总数据,分割剂量≥1 Gy时α/β值为2.3 Gy(95%置信区间,0.82,3.7 Gy),0.8、0.6和0.4 Gy实验的α/β值为1.2 Gy(95%置信区间,0.16,2.3 Gy)。(摘要截短至250字)