Garcia Darwin A, Fazzari Jennifer M, Hlushchuk Ruslan, Khoma Oleksiy-Zakhar, Bakken Katrina K, Burgenske Danielle M, Lester Scott C, Mutter Robert W, Lucien Fabrice, Remmes Nicholas B, Sarkaria Jann N, Park Sean S, Djonov Valentin G, Grams Michael P
Department of Radiation Oncology, Mayo Clinic, Rochester, Minnesota.
Department of Radiation Oncology, Mayo Clinic, Rochester, Minnesota; Department of Anatomy, University of Bern, Bern, Switzerland.
Int J Radiat Oncol Biol Phys. 2025 Mar 15. doi: 10.1016/j.ijrobp.2025.03.016.
Minibeam radiation therapy (MBRT) is an innovative strategy to improve normal tissue sparing by delivering alternating, submillimeter-wide regions of high "peak" and low "valley" doses. The purpose of this study was to characterize both acute and late MBRT-induced normal tissue toxicities and determine the dosimetric parameters that dictate toxicity.
Mice were stratified by weight and randomized to receive a single dose of conventional radiation therapy (uniform open field) or MBRT (0.5 mm-wide minibeams spaced 1.1 mm center to center) to the oral cavity. The conventional RT groups (n = 4 per group) received 16 or 20 Gy, whereas the MBRT groups (n = 5 per group) received peak:valley doses of 48:8, 72:12, 96:8, 96:16, or 152:8 Gy. Acute toxicity (≤3 weeks) was evaluated using changes in weight and mucosal histology. Late effects on bone and dentition were evaluated using microscopic computed tomography (microCT).
Animals irradiated with 16 Gy (n = 1), 20 Gy (n = 4), and 96:16 Gy (n = 5) reached acute toxicity endpoint (≥20% weight loss) between 9 and 11 days postradiation and exhibited histologic changes indicative of mucositis. No animals in the other MBRT groups reached acute toxicity endpoint. Although 96:8 Gy induced marked mucosal damage in peak regions, the spared tissue in the valley regions enabled restoration of mucosal integrity within 2 weeks post-MBRT. MicroCT of surviving mice 12 months postradiation revealed an alternating pattern of decreased bone volume consistent with the MBRT pattern. The upper incisors of most animals were shortened or completely missing. The mice receiving 16 Gy and 48:8 Gy exhibited the most and least dental damage, respectively.
This preliminary study emphasizes that normal tissue sparing by MBRT, as determined by the valley dose, significantly ameliorates dose-limiting toxicities and enables escalation to MBRT peak doses up to an order of magnitude greater than conventional RT doses.
微束放射治疗(MBRT)是一种创新策略,通过交替给予亚毫米宽的高“峰值”和低“谷值”剂量区域来提高正常组织的保护。本研究的目的是描述MBRT引起的急性和晚期正常组织毒性,并确定决定毒性的剂量学参数。
将小鼠按体重分层,随机分为接受单剂量传统放射治疗(均匀开放野)或MBRT(中心间距1.1 mm的0.5 mm宽微束)照射口腔。传统放疗组(每组n = 4)接受16或20 Gy照射,而MBRT组(每组n = 5)接受峰值:谷值剂量为48:8、72:12、96:8、96:16或152:8 Gy的照射。使用体重变化和黏膜组织学评估急性毒性(≤3周)。使用显微计算机断层扫描(microCT)评估对骨骼和牙列的晚期影响。
接受16 Gy(n = 1)、20 Gy(n = 4)和96:16 Gy(n = 5)照射的动物在放疗后9至11天达到急性毒性终点(体重减轻≥20%),并表现出提示黏膜炎的组织学变化。其他MBRT组中没有动物达到急性毒性终点。尽管96:8 Gy在峰值区域引起明显的黏膜损伤,但谷值区域的 spared组织使MBRT后2周内黏膜完整性得以恢复。放疗后12个月存活小鼠的microCT显示骨体积减少的交替模式与MBRT模式一致。大多数动物的上门牙缩短或完全缺失。接受16 Gy和48:8 Gy照射的小鼠分别表现出最严重和最轻微的牙齿损伤。
这项初步研究强调,由谷值剂量决定的MBRT对正常组织的保护可显著减轻剂量限制毒性,并使MBRT峰值剂量能够增加到比传统放疗剂量大一个数量级。