Abstract
About 10 years ago, the first studies supporting the hypothesis that the response of prostate cancer to radiation was similar to that of slow-proliferating normal tissues were published. However, hypofractionation has been a common practice throughout radiotherapy history, mainly in western countries. The results of both experimental and clinical studies suggest that the α/β ratio for prostate cancer cells is lower than the α/β ratio for late-responding cells of the rectum and the bladder. This particularity allows the therapeutic window to be increased through the use of hypofractionated schemes. It has also been possible to establish, based on late toxicity results, that hypofractionated regimens are safe, and even without the use of IMRT or IGRT technology, the slight increases in acute toxicity found in some studies has been well tolerated. Nevertheless, to date, hypofractionation has not proved to be superior to conventionally fractionated therapy in terms of tumor control. Hypofractionation studies have so far been limited by their relatively short follow-up, a modest increase in dose per fraction (usually 2.5–3 Gy), and the difficulty to establish comparisons among different radiation techniques, hypofractionation schemes, and toxicity scales.
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Hernandez, V.M. (2012). Hypofractionated Radiation Therapy in Prostate Cancer: Rationale, History, and Outcomes. In: Ponsky, L., Fuller, D., Meier, R., Ma, C. (eds) Robotic Radiosurgery. Treating Prostate Cancer and Related Genitourinary Applications. Springer, Berlin, Heidelberg. https://doi.org/10.1007/978-3-642-11495-3_9
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