FLASH proton reirradiation, with or without hypofractionation, mitigates chronic toxicity in the normal murine intestine, skin, and bone.

Verginadis, I. I.; Velalopoulou, A.; Kim, M. M.; Kim, K.; Paraskevaidis, I.; Bell, B.; Oliaei Motlagh, S. A.; Karaj, A.; Banerjee, E.; Finesso, G. E.; Assenmacher, C.-A.; Radaelli, E.; Lu, J.; Lin, Y.; Putt, M. E.; Diffenderfer, E. S.; Guha, C.; Qin, L.; Metz, J. M.; Maity, A.; Cengel, K. A.; Koumenis, C.; Busch, T. M.

doi:10.1101/2024.07.08.602528

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bioRxiv · 10.1101/2024.07.08.602528

FLASH proton reirradiation, with or without hypofractionation, mitigates chronic toxicity in the normal murine intestine, skin, and bone.

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Abstract

Background and purposeThe normal tissue sparing afforded by FLASH radiotherapy (RT) is being intensely investigated for potential clinical translation. Here, we studied the effects of FLASH proton RT (F-PRT) in the reirradiation setting, with or without hypofractionation. Chronic toxicities in three murine models of normal tissue toxicity including the intestine, skin, and bone were investigated. Materials and methodsIn studies of the intestine, single-dose irradiation was performed with 12 Gy of Standard proton RT (S-PRT), followed by a second dose of 12 Gy of F-PRT or S-PRT. Additionally, a hypofractionation scheme was applied in the reirradiation setting (3 x 6.4 Gy of F-PRT or S-PRT, given every 48 hrs). In studies of skin/bone of the murine leg, 15 Gy of S-PRT was followed by hypofractionated reirradiation with F-PRT or S-PRT (3 x 11 Gy). ResultsCompared to reirradiation with S-PRT, F-PRT reduced intestinal fibrosis and collagen deposition in the reirradiation setting and significantly increased survival rate, demonstrating its protective effects on intestinal tissues. In previously irradiated leg tissues, reirradiation with hypofractionated F-PRT created transient dermatitis that fully resolved in contrast to reirradiation with hypofractionated S-PRT. Lymphedema was also alleviated after a second course of radiation with F-PRT, along with significant reductions in the accumulation of fibrous connective tissue in the skin compared to mice reirradiated with S-PRT. The delivery of a second course of fractionated S-PRT induced tibial fractures in 83.3% of the mice, whereas only 20% of mice reirradiated with F-PRT presented with fractures. ConclusionThese studies provide the first evidence of the sparing effects of F-PRT, in the setting of hypofractionated reirradiation. The results support FLASH as highly relevant to the reirradiation regimen where it exhibits significant potential to minimize chronic complications for patients undergoing RT.

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Verginadis, I. I., Velalopoulou, A., Kim, M. M., Kim, K., Paraskevaidis, I., Bell, B., Oliaei Motlagh, S. A., Karaj, A., Banerjee, E., Finesso, G. E., Assenmacher, C.-A., Radaelli, E., Lu, J., Lin, Y., Putt, M. E., Diffenderfer, E. S., Guha, C., Qin, L., Metz, J. M., Maity, A., Cengel, K. A., Koumenis, C., Busch, T. M.. 2024-07-11. FLASH proton reirradiation, with or without hypofractionation, mitigates chronic toxicity in the normal murine intestine, skin, and bone.. https://doi.org/10.1101/2024.07.08.602528

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