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Spinal cord tolerance to single-session uniform irradiation in pigs: Implications for a dose-volume effect
Abstract Background and purpose This study was performed to test the hypothesis that spinal cord radiosensitivity is significantly modified by uniform versus laterally non-uniform dose distributions. Materials and methods A uniform dose distribution was delivered to a 4.5–7.0 cm length of cervical s...
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Published in: | Radiotherapy and oncology 2013-01, Vol.106 (1), p.101-105 |
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Main Authors: | , , , , , |
Format: | Article |
Language: | English |
Subjects: | |
Citations: | Items that this one cites Items that cite this one |
Online Access: | Get full text |
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Summary: | Abstract Background and purpose This study was performed to test the hypothesis that spinal cord radiosensitivity is significantly modified by uniform versus laterally non-uniform dose distributions. Materials and methods A uniform dose distribution was delivered to a 4.5–7.0 cm length of cervical spinal cord in 22 mature Yucatan minipigs for comparison with a companion study in which a laterally non-uniform dose was given [1] . Pigs were allocated into four dose groups with mean maximum spinal cord doses of 17.5 ± 0.1 Gy ( n = 7), 19.5 ± 0.2 Gy ( n = 6), 22.0 ± 0.1 Gy ( n = 5), and 24.1 ± 0.2 Gy ( n = 4). The study endpoint was motor neurologic deficit determined by a change in gait within one year. Spinal cord sections were stained with a Luxol fast blue/periodic acid Schiff combination. Results Dose–response curves for uniform versus non-uniform spinal cord irradiation were nearly identical with ED50 ’s (95% confidence interval) of 20.2 Gy (19.1–25.8) and 20.0 Gy (18.3–21.7), respectively. No neurologic change was observed for either dose distribution when the maximum spinal cord dose was ⩽17.8 Gy while all animals experienced deficits at doses ⩾21.8 Gy. Conclusion No dose-volume effect was observed in pigs for the dose distributions studied and the endpoint of motor neurologic deficit; however, partial spinal cord irradiation resulted in less debilitating neurologic morbidity and histopathology. |
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ISSN: | 0167-8140 1879-0887 |
DOI: | 10.1016/j.radonc.2012.08.007 |