The study investigated the effects of proton minibeam radiotherapy (pMBRT) on DNA damage in a human epidermis model, using minibeams of varying widths (66 µm, 408 µm, and 920 µm) and a consistent inter-beam distance. Results showed that the 66 µm minibeams caused sharply localized severe DNA damage at dose peaks, while wider beams affected all cells. DNA damage was repaired by 72 hours post-irradiation, but increased cell death markers were observed at later time points. The findings suggested that pMBRT could minimize skin side effects in radiotherapy due to its spatially confined DNA damage, making it a promising approach for reducing radiotherapy side effects.
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October 2008 in “Journal der Deutschen Dermatologischen Gesellschaft” Anti-cancer treatments can cause reversible hair loss, skin sensitivity, pigmentation changes, nail damage, and skin reactions, with a need for more research on managing these side effects.
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January 2023 in “Skin appendage disorders” A woman's hair grew back after treatment for a rare hair loss caused by proton therapy.