Institut Curie, PSL Research University, Radiation Oncology Department, Proton Therapy Centre, Centre Universitaire, Orsay, France; Institut Curie, PSL Research University, University Paris Saclay, Inserm LITO, Orsay, France.
Laboratoire de Physique Corpusculaire/IN2P3-CNRS UMR 6534-ARCHADE, Unicaen-Université de Normandie, Caen, France.
Int J Radiat Oncol Biol Phys. 2022 Aug 1;113(5):985-995. doi: 10.1016/j.ijrobp.2022.02.009. Epub 2022 Feb 26.
For many years, the effect of dose rate (DR) was considered negligible in external beam radiation therapy (EBRT) until very-high DR (>10 Gy/min) became possible and ultrahigh DR (>40 Gy/s) showed dramatic protection of normal tissues in preclinical experiments. We propose a critical review of preclinical and clinical studies to investigate the biological and clinical effects of DR variation in the range covering brachytherapy to flattening filter free EBRT and FLASH.
Preclinical and clinical studies investigating biological and clinical DR effects were reviewed extensively. We also conducted an in silico study to assess the effect of pulse DR (DR), taking into account the mean time between 2 tracks during the pulse.
Preclinical studies have shown that an increase in DR in the range of 0.01 to 20 Gy/min (not including ultralow or ultrahigh DR) resulted in decreased survival of both normal and tumor cells. This effect was attributed primarily to increasingly unrepaired "sublethal" DNA damage with increasing the DR. However, the models and irradiation conditions have often been very different from one radiobiological study to another. Moreover, the physical parameters on the spatial and temporal microstructure of the beam were not considered systematically. In particular, the DR was rarely mentioned. The in silico studies showed that for the same average DR, increasing DR induced an increase of mean track rates. These results could explain the presence of more complex damage when the DR was increased within the range of DR considered, in relation to the time-dependent probability of accumulating unrepaired, "sublethal" DNA lesions in close proximity.
Knowledge of the beam microstructure is critical to understanding the biological impact and the clinical outcomes of radiation at the DR commonly used in radiation therapy.
多年来,在非常高的剂量率(>10Gy/min)成为可能且超高剂量率(>40Gy/s)在临床前实验中显示出对正常组织的显著保护作用之前,外束放射治疗(EBRT)中的剂量率(DR)效应被认为可以忽略不计。我们提出了对临床前和临床研究的批判性回顾,以研究涵盖近距离放射治疗到无均整滤过器的 EBRT 和 FLASH 的范围内的 DR 变化的生物学和临床影响。
广泛回顾了研究生物学和临床 DR 效应的临床前和临床研究。我们还进行了一项计算机模拟研究,以评估脉冲剂量率(DR)的影响,同时考虑到脉冲期间两个轨迹之间的平均时间。
临床前研究表明,在 0.01 至 20Gy/min 的剂量率范围内(不包括超低或超高剂量率)增加剂量率会导致正常和肿瘤细胞的存活率降低。这种效应主要归因于随着剂量率的增加,越来越多的未修复的“亚致死”DNA 损伤。然而,模型和照射条件往往在一个放射生物学研究与另一个研究之间有很大的不同。此外,光束的空间和时间微观结构的物理参数没有被系统地考虑。特别是,剂量率很少被提及。计算机模拟研究表明,对于相同的平均剂量率,增加剂量率会导致平均轨迹速率增加。这些结果可以解释在考虑范围内增加剂量率时,由于时间相关的未修复“亚致死”DNA 损伤在近距离处积累的概率,存在更复杂的损伤。
了解光束微观结构对于理解放射治疗中常用的 DR 的生物学影响和临床结果至关重要。