Kasamatsu Koki, Matsuura Taeko, Tanaka Sodai, Takao Seishin, Miyamoto Naoki, Nam Jin-Min, Shirato Hiroki, Shimizu Shinichi, Umegaki Kikuo
Graduate School of Biomedical Science and Engineering, Hokkaido University, Sapporo, Hokkaido, 0608638, Japan.
Division of Quantum Science and Engineering, Faculty of Engineering, Hokkaido University, Sapporo, Hokkaido, 0608628, Japan.
Med Phys. 2020 Sep;47(9):4644-4655. doi: 10.1002/mp.14381. Epub 2020 Aug 2.
The purpose of this study is to evaluate the sublethal damage (SLD) repair effect in prolonged proton irradiation using the biophysical model with various cell-specific parameters of (α/β) and T (repair half time). At present, most of the model-based studies on protons have focused on acute radiation, neglecting the reduction in biological effectiveness due to SLD repair during the delivery of radiation. Nevertheless, the dose-rate dependency of biological effectiveness may become more important as advanced treatment techniques, such as hypofractionation and respiratory gating, come into clinical practice, as these techniques sometimes require long treatment times. Also, while previous research using the biophysical model revealed a large repair effect with a high physical dose, the dependence of the repair effect on cell-specific parameters has not been evaluated systematically.
Biological dose [relative biological effectiveness (RBE) × physical dose] calculation with repair included was carried out using the linear energy transfer (LET)-dependent linear-quadratic (LQ) model combined with the theory of dual radiation action (TDRA). First, we extended the dose protraction factor in the LQ model for the arbitrary number of different LET proton irradiations delivered sequentially with arbitrary time lags, referring to the TDRA. Using the LQ model, the decrease in biological dose due to SLD repair was systematically evaluated for spread-out Bragg peak (SOBP) irradiation in a water phantom with the possible ranges of both (α/β) and repair parameters ((α/β) = 1-15 Gy, T = 0-90 min). Then, to consider more realistic irradiation conditions, clinical cases of prostate, liver, and lung tumors were examined with the cell-specific parameters for each tumor obtained from the literature. Biological D and biological dose homogeneity coefficient (HC) were calculated for the clinical target volumes (CTVs), assuming dose-rate structures with a total irradiation time of 0-60 min.
The differences in the cell-specific parameters resulted in considerable variation in the repair effect. The biological dose reduction found at the center of the SOBP with 30 min of continuous irradiation varied from 1.13% to 14.4% with a T range of 1-90 min when (α/β) is fixed as 10 Gy. It varied from 2.3% to 6.8% with an (α/β) range of 1-15 Gy for a fixed value of T = 30 min. The decrease in biological D per 10 min was 2.6, 1.2, and 3.0% for the prostate, liver, and lung tumor cases, respectively. The value of the biological D reduction was neither in the order of (α/β) nor prescribed dose, but both comparably contributed to the repair effect. The variation of HC was within the range of 0.5% for all cases; therefore, the dose distribution was not distorted.
The reduction in biological dose caused by the SLD repair largely depends on the cell-specific parameters in addition to the physical dose. The parameters should be considered carefully in the evaluation of the repair effect in prolonged proton irradiation.
本研究旨在使用生物物理模型,结合不同细胞特异性参数(α/β)和T(修复半衰期),评估质子长时间照射下的亚致死损伤(SLD)修复效果。目前,大多数基于模型的质子研究都集中在急性辐射上,忽略了辐射过程中由于SLD修复导致的生物学效应降低。然而,随着诸如大分割放疗和呼吸门控等先进治疗技术应用于临床实践,生物学效应的剂量率依赖性可能变得更加重要,因为这些技术有时需要较长的治疗时间。此外,虽然先前使用生物物理模型的研究显示在高物理剂量下有较大的修复效果,但修复效果对细胞特异性参数的依赖性尚未得到系统评估。
采用与双辐射作用理论(TDRA)相结合的依赖线性能量传递(LET)的线性二次(LQ)模型,进行包含修复的生物剂量[相对生物效应(RBE)×物理剂量]计算。首先,参考TDRA,我们将LQ模型中的剂量延长因子扩展到任意数量的不同LET质子照射,这些照射以任意时间间隔顺序进行。使用LQ模型,在水模体中针对扩展布拉格峰(SOBP)照射,系统评估了在(α/β)和修复参数(α/β = 1 - 15 Gy,T = 0 - 90分钟)的可能范围内,由于SLD修复导致的生物剂量降低。然后,为考虑更实际的照射条件,利用从文献中获得的每种肿瘤的细胞特异性参数,对前列腺、肝脏和肺部肿瘤的临床病例进行了研究。假设总照射时间为0 - 60分钟的剂量率结构,计算了临床靶区(CTV)的生物D和生物剂量均匀性系数(HC)。
细胞特异性参数的差异导致修复效果有显著变化。当(α/β)固定为10 Gy时,在SOBP中心连续照射30分钟时,生物剂量降低在T范围为1 - 90分钟时从1.13%变化到14.4%。对于固定的T = 30分钟,在α/β范围为1 - 15 Gy时,生物剂量降低从2.3%变化到6.8%。前列腺、肝脏和肺部肿瘤病例每10分钟生物D的降低分别为2.6%、1.2%和3.0%。生物D降低值既不按(α/β)顺序也不按规定剂量排列,但两者对修复效果的贡献相当。所有病例中HC的变化在0.5%范围内;因此,剂量分布未发生畸变。
除物理剂量外,SLD修复导致的生物剂量降低在很大程度上取决于细胞特异性参数。在评估质子长时间照射下的修复效果时,应仔细考虑这些参数。