Department of Obstetrics and Gynaecology, University of Melbourne, Royal Women's Hospital, Parkville, Victoria, 3052, Australia.
School of Science, RMIT University, Melbourne, Victoria, 3001, Australia.
Sci Rep. 2018 Aug 13;8(1):12044. doi: 10.1038/s41598-018-30543-1.
Synchrotron radiation can facilitate novel radiation therapy modalities such as microbeam radiation therapy (MRT) and high dose-rate synchrotron broad-beam radiation therapy (SBBR). Both of these modalities have unique physical properties that could be exploited for an improved therapeutic effect. While pre-clinical studies report promising normal tissue sparing phenomena, systematic toxicity data are still required. Our objective was to characterise the toxicity of SBBR and MRT and to calculate equivalent doses of conventional radiation therapy (CRT). A dose-escalation study was performed on C57BLJ/6 mice using total body and partial body irradiations. Dose-response curves and TD values were subsequently calculated using PROBIT analysis. For SBBR at dose-rates of 37 to 41 Gy/s, we found no evidence of a normal tissue sparing effect relative to CRT. Our findings also show that the MRT valley dose, rather than the peak dose, best correlates with CRT doses for acute toxicity. Importantly, longer-term weight tracking of irradiated animals revealed more pronounced growth impairment following MRT compared to both SBBR and CRT. Overall, this study provides the first in vivo dose-equivalence data between MRT, SBBR and CRT and presents systematic toxicity data for a range of organs that can be used as a reference point for future pre-clinical work.
同步辐射可以促进新的放射治疗方式,如微束放射治疗(MRT)和高剂量率同步宽束放射治疗(SBBR)。这两种方式都具有独特的物理特性,可以用于提高治疗效果。虽然临床前研究报告了有希望的正常组织保护现象,但仍需要系统的毒性数据。我们的目的是描述 SBBR 和 MRT 的毒性,并计算常规放射治疗(CRT)的等效剂量。我们在 C57BLJ/6 小鼠上进行了全身和局部照射的剂量递增研究。随后使用 PROBIT 分析计算剂量反应曲线和 TD 值。对于剂量率为 37 至 41 Gy/s 的 SBBR,我们没有发现相对于 CRT 的正常组织保护效应的证据。我们的研究结果还表明,对于急性毒性,MRT 的谷底剂量而不是峰值剂量与 CRT 剂量相关性最好。重要的是,对受照射动物的长期体重跟踪显示,MRT 后生长受损比 SBBR 和 CRT 更为明显。总的来说,这项研究提供了 MRT、SBBR 和 CRT 之间的首次体内剂量等效数据,并提供了一系列器官的系统毒性数据,可作为未来临床前工作的参考点。