2009
DOI: 10.1016/j.ejca.2009.07.009
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Acute toxicity of curative radiotherapy for intermediate- and high-risk localised prostate cancer in the EORTC trial 22991

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Cited by 73 publications
(35 citation statements)
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“…In terms of acute GI and GU toxicities $grade 2, the rates reported from PO IMRT series are from 1.9% to 32.4% and 9-64%, respectively. 10,[24][25][26][27][28] For WP IMRT, acute GI and GU toxicities $grade 2 have been reported from 12% to 50% and 44-51.7%, respectively. 10,[28][29][30] Although the use of different toxicity scales makes comparison difficult, in our study, both PO and WP VMAT with daily CBCT-based IGRT provided acceptably low rates of acute GI and GU toxicity when compared with the results presented in other studies.…”
Section: Discussionmentioning
confidence: 99%
“…In terms of acute GI and GU toxicities $grade 2, the rates reported from PO IMRT series are from 1.9% to 32.4% and 9-64%, respectively. 10,[24][25][26][27][28] For WP IMRT, acute GI and GU toxicities $grade 2 have been reported from 12% to 50% and 44-51.7%, respectively. 10,[28][29][30] Although the use of different toxicity scales makes comparison difficult, in our study, both PO and WP VMAT with daily CBCT-based IGRT provided acceptably low rates of acute GI and GU toxicity when compared with the results presented in other studies.…”
Section: Discussionmentioning
confidence: 99%
“…Rates of grade1 GI toxicities reported in CF-EBRT studies ranged from 16.1 to 51.1% (30)(31)(32), grade 2 from 6.3 to 20.7% and grade 3 from 0 to 9%. One CF-EBRT study neglected to stratify rates of acute GI toxicity by grade (29); it reported that 25% of patients treated EBRT experienced grade 2 or higher GI toxicity.…”
Section: Resultsmentioning
confidence: 99%
“…Rates of grade1 GU toxicity reported in CF-EBRT (n=1118) studies ranged from 28.7 to 51.9% (30)(31)(32), grade 2 from 15.6 to 41.4% and grade 3 from 1.1 to 8%. Two grade 4 acute GU toxicities were reported, a rate of 0.001% in the overall cohort.…”
Section: Resultsmentioning
confidence: 99%
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“…[6] Bu erken yan etkilerin hastaların yaşam kalitesini olumsuz yönde etkilediği ve bazı çalışmalarda geç yan etkilere predispozan olduğu bildirilmiştir. [7][8][9] Prostat kanseri tedavisinde IMRT tekniği ile doz yükseltilmesinin lokal ve biyokimyasal kontrol ve tedaviye bağlı toksisite açısından 3BKRT'ye göre üstünlüğü çeşitli çalışmalarla gösterilmiştir [10][11][12][13][14][15] . Bu nedenle günümüzde yüksek doz IMRT erken ve lokal ileri prostat kanserinde önerilen standart tedavidir.…”
Section: Sonuçunclassified