Department of Neurosurgery, Johns Hopkins University School of Medicine, Baltimore, Maryland.
Department of Chemical and Biomedical Engineering, Florida A&M University-Florida State University College of Engineering, Tallahassee, Florida.
Int J Radiat Oncol Biol Phys. 2021 Oct 1;111(2):528-538. doi: 10.1016/j.ijrobp.2021.04.050. Epub 2021 May 11.
Vertebral compression fracture is a common complication of spinal stereotactic body radiation therapy. Development of an in vivo model is crucial to fully understand how focal radiation treatment affects vertebral integrity and biology at various dose fractionation regimens. We present a clinically relevant animal model to analyze the effects of localized, high-dose radiation on vertebral microstructure and mechanical integrity. Using this model, we test the hypothesis that fractionation of radiation dosing can reduce focused radiation therapy's harmful effects on the spine.
The L5 vertebra of New Zealand white rabbits was treated with either a 24-Gy single dose of focused radiation or 3 fractionated 8-Gy doses over 3 consecutive days via the Small Animal Radiation Research Platform. Nonirradiated rabbits were used as controls. Rabbits were euthanized 6 months after irradiation, and their lumbar vertebrae were harvested for radiologic, histologic, and biomechanical testing.
Localized single-dose radiation led to decreased vertebral bone volume and trabecular number and a subsequent increase in trabecular spacing and thickness at L5. Hypofractionation of the radiation dose similarly led to reduced trabecular number and increased trabecular spacing and thickness, yet it preserved normalized bone volume. Single-dose irradiated vertebrae displayed lower fracture loads and stiffness compared with those receiving hypofractionated irradiation and with controls. The hypofractionated and control groups exhibited similar fracture load and stiffness. For all vertebral samples, bone volume, trabecular number, and trabecular spacing were correlated with fracture loads and Young's modulus (P < .05). Hypocellularity was observed in the bone marrow of both irradiated groups, but osteogenic features were conserved in only the hypofractionated group.
Single-dose focal irradiation showed greater detrimental effects than hypofractionation on the microarchitectural, cellular, and biomechanical characteristics of irradiated vertebral bodies. Correlation between radiologic measurements and biomechanical properties supported the reliability of this animal model of radiation-induced vertebral compression fracture, a finding that can be applied to future studies of preventative measures.
脊柱立体定向体部放射治疗后常发生椎体压缩性骨折。建立一种体内模型对于充分了解不同分割剂量的聚焦放射治疗对椎体完整性和生物学的影响至关重要。我们提出了一种临床相关的动物模型,以分析局部高剂量照射对椎体微观结构和机械完整性的影响。使用该模型,我们检验了这样一个假设,即分次放射剂量可以降低聚焦放射治疗对脊柱的有害影响。
新西兰白兔的 L5 椎体接受 24 Gy 单次剂量聚焦放射治疗或 3 天内 3 次 8 Gy 分割剂量照射,采用小动物放射研究平台进行。未照射的兔子作为对照。照射后 6 个月处死兔子,取其腰椎进行放射学、组织学和生物力学测试。
局部单次照射导致 L5 椎体骨体积和小梁数量减少,随后小梁间距和厚度增加。放射剂量的亚分割同样导致小梁数量减少和小梁间距及厚度增加,但保持了正常的骨体积。与接受亚分割照射和对照组相比,单次照射的椎体显示出较低的骨折负荷和刚度。亚分割照射组和对照组的骨折负荷和刚度相似。对于所有椎体样本,骨体积、小梁数量和小梁间距与骨折负荷和杨氏模量呈正相关(P <.05)。两组照射后的骨髓均出现低细胞性,但仅在亚分割照射组保留了成骨特征。
与亚分割照射相比,单次聚焦照射对受照射椎体的微观结构、细胞和生物力学特性具有更大的不利影响。放射学测量与生物力学特性之间的相关性支持了这种放射诱导椎体压缩性骨折动物模型的可靠性,这一发现可应用于未来的预防措施研究。