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dc.creatorAlexidis P., Karatzoglou S., Dragoumis D., Drevelegas K., Tzitzikas I., Hatzimouratidis K., Chrisogonidis I., Ioannidis A., Katsios I.N., Zarogoulidis P., Sapalidis K., Koulouris C., Michalopoulos N., Giannakidis D., Aidoni Z., Fyntanidou V., Amaniti A., Boniou K., Kesisoglou I., Vagionas A., Romanidis K., Oikonomou P., Goganau A.M., Petanidis S., Maragouli E., Kosmidis C.en
dc.date.accessioned2023-01-31T07:30:51Z
dc.date.available2023-01-31T07:30:51Z
dc.date.issued2020
dc.identifier10.7150/jca.37825
dc.identifier.issn18379664
dc.identifier.urihttp://hdl.handle.net/11615/70416
dc.description.abstractBackground: Prostate cancer is considered to be highly sensitive to changes in radiation therapy dose per fraction, specifically to hypofractionation. An increase in the fractionation dose could cause a higher increase to the prostate than to the normal tissues leading to better disease control with less toxicity. Here we present the results of a randomized trial comparing mild hypofractionation to conventional fractionation after a median of 3,6 years follow up. Patients and Methods: 139 patients were randomized to receive either hypofractionated radiotherapy with 2,25 Gy/fr to a total of 72 Gy (arm 1) or conventionally fractionated treatment with 2Gy/fr to a total of 74 Gy (arm 2). 72 patients were assigned to arm 1 and 67 to arm 2. Results: After a median follow up of 3,6 years, 23 patients (31,9%) from arm 1 developed grade≥ 2 acute genitourinary toxicity and 21 (31,3%) from arm 2 (p=0,79). The corresponding values from gastrointestinal were 15 (20,8%) and 12 (17,9%) (p=0,6). For late toxicity from GU, 8 patients (11,1%) developed grade≥ 2 symptoms in arm 1 and 7 (10,4%) in arm 2 (p=0,92). late GI toxicity grade≥ 2 was observed in 8 (11,1%) patients in arm 1 and 8 (11,9%) in arm 2 (p=0,88). In multivariate analysis, hormone therapy was significantly associated with late GI events, while acute toxicity from both GU and GI was a prognostic factor of late adverse reaction. Conclusion: No difference in the toxicity profile could be identified between hypofractionation and conventional fractionation. Our schedule of 2,25Gy/fr seems safe and tolerable by the patients with acceptable rates of acute and late toxicity. © The author(s).en
dc.language.isoenen
dc.sourceJournal of Canceren
dc.source.urihttps://www.scopus.com/inward/record.uri?eid=2-s2.0-85078060667&doi=10.7150%2fjca.37825&partnerID=40&md5=33562d2934fa5832072fdd77e3563ed7
dc.subjectantiandrogenen
dc.subjectgonadorelin derivativeen
dc.subjectprostate specific antigenen
dc.subjectacute toxicityen
dc.subjectadulten
dc.subjectageden
dc.subjectandrogen deprivation therapyen
dc.subjectArticleen
dc.subjectcancer hormone therapyen
dc.subjectcancer prognosisen
dc.subjectcancer radiotherapyen
dc.subjectcombination drug therapyen
dc.subjectcomparative studyen
dc.subjectcontrolled studyen
dc.subjectfollow upen
dc.subjectgastrointestinal symptomen
dc.subjecthigh risk patienten
dc.subjecthumanen
dc.subjecthypofractionated radiotherapyen
dc.subjectintensity modulated radiation therapyen
dc.subjectlow risk patienten
dc.subjectmajor clinical studyen
dc.subjectmaleen
dc.subjectplanning target volumeen
dc.subjectprostate canceren
dc.subjectquality of lifeen
dc.subjectradiation injuryen
dc.subjectradiotherapy dosageen
dc.subjectrandomized controlled trialen
dc.subjectseminal vesicleen
dc.subjecturinary tract infectionen
dc.subjecturogenital tract diseaseen
dc.subjectIvyspring International Publisheren
dc.titleLate results of a randomized trial on the role of mild hypofractionated radiotherapy for the treatment of localized prostate canceren
dc.typejournalArticleen


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