Minibeam Radiation Therapy Valley Dose Determines Tolerance to Acute and Late Effects in the Mouse Oral Cavity

IF 6.5 1区 医学 Q1 ONCOLOGY International Journal of Radiation Oncology Biology Physics Pub Date : 2025-09-01 Epub Date: 2025-03-15 DOI:10.1016/j.ijrobp.2025.03.016
Darwin A. Garcia PhD , Jennifer M. Fazzari PhD , Ruslan Hlushchuk MD , Oleksiy-Zakhar Khoma MS , Katrina K. Bakken CVT , Danielle M. Burgenske PhD , Scott C. Lester MD , Robert W. Mutter MD , Fabrice Lucien PhD , Nicholas B. Remmes PhD , Jann N. Sarkaria MD , Sean S. Park MD, PhD , Valentin G. Djonov MD , Michael P. Grams PhD
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Abstract

Purpose

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.

Methods and Materials

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).

Results

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.

Conclusions

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.
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迷你束放射治疗谷剂量决定了小鼠口腔对急性和晚期效应的耐受性。
目的:微束放疗(MBRT)是一种创新的策略,通过提供交替的亚毫米宽区域的高“峰”和低“谷”剂量来改善正常组织的保留。这项工作的目的是表征急性和晚期mbrt诱导的正常组织毒性,并确定指示毒性的剂量学参数。方法和材料:小鼠按体重分层,随机接受单剂量常规放疗(均匀开场)或MBRT (0.5 mm宽、中心间隔1.1 mm的微束)到口腔。常规RT组(n=4 /组)接受16或20 Gy,而MBRT组(n=5 /组)接受峰谷剂量分别为48:8、72:12、96:8、96:16或152:8 Gy。急性毒性(≤3周)通过体重和黏膜组织学变化进行评估。使用显微计算机断层扫描(microCT)评估对骨和牙列的晚期影响。结果:接受16 Gy (n=1)、20 Gy (n=4)和96:16 Gy (n=5)放射治疗的动物在放射后9-11天达到急性毒性终点(体重减轻≥20%),并表现出黏膜炎的组织学改变。其他MBRT组没有动物达到急性毒性终点。虽然96:8 Gy在峰值区诱导了明显的粘膜损伤,但在谷区留下的组织使mbrt后两周内粘膜完整性得以恢复。放疗后12个月存活小鼠的微ct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。剂量为16 Gy和48:8 Gy的小鼠牙损伤最大、最小。结论:这项初步工作强调,由谷剂量决定的MBRT对正常组织的保留,显著改善了剂量限制性毒性,并使MBRT的峰值剂量增加到比常规RT剂量大的数量级。
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来源期刊
CiteScore
11.00
自引率
7.10%
发文量
2538
审稿时长
6.6 weeks
期刊介绍: International Journal of Radiation Oncology • Biology • Physics (IJROBP), known in the field as the Red Journal, publishes original laboratory and clinical investigations related to radiation oncology, radiation biology, medical physics, and both education and health policy as it relates to the field. This journal has a particular interest in original contributions of the following types: prospective clinical trials, outcomes research, and large database interrogation. In addition, it seeks reports of high-impact innovations in single or combined modality treatment, tumor sensitization, normal tissue protection (including both precision avoidance and pharmacologic means), brachytherapy, particle irradiation, and cancer imaging. Technical advances related to dosimetry and conformal radiation treatment planning are of interest, as are basic science studies investigating tumor physiology and the molecular biology underlying cancer and normal tissue radiation response.
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