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The impact of bladder preparation protocols on post treatment toxicity in radiotherapy for localised prostate cancer patients

OBJECTIVE: This study compares the post radiotherapy related toxicity between the use of an empty and a full bladder preparation protocol in patients receiving radical radiotherapy for localised prostate cancer. METHODS AND MATERIALS: A retrospective review of patient treatment records in which they...

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Autores principales: Tsang, Yat Man, Hoskin, Peter
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7033795/
https://www.ncbi.nlm.nih.gov/pubmed/32095565
http://dx.doi.org/10.1016/j.tipsro.2017.10.001
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author Tsang, Yat Man
Hoskin, Peter
author_facet Tsang, Yat Man
Hoskin, Peter
author_sort Tsang, Yat Man
collection PubMed
description OBJECTIVE: This study compares the post radiotherapy related toxicity between the use of an empty and a full bladder preparation protocol in patients receiving radical radiotherapy for localised prostate cancer. METHODS AND MATERIALS: A retrospective review of patient treatment records in which they were treated with a standard radiotherapy schedule (60Gy/20 fractions) to prostates and base of seminal vesicles only and followed two different bladder preparation (empty and full) protocols was carried out. This included each patient's daily image guided radiotherapy (IGRT) setup, treatment time, bladder size on planning computed tomography, organs at risk dose volume histograms (OAR DVHs) and 12 months post treatment gastrointestinal (GI) and genitourinary (GU) toxicity data. RESULTS: 20 patients were included. There were significant differences in IGRT setup between the two groups. Although treatment times of the two groups were not significantly different, 5/200 (2.5%) sessions were longer than 20 min in the full bladder group while this was not found in the other group. Associations between bladder preparation protocols and GI (p = 1.0) and GU (p = 0.6) toxicities were not statistically significant. The bladder size on planning CT was not significantly correlated to the GI (R = 0.06, p = 0.8) or GU (R = 0.27, p = 0.3) toxicity scores. No significant differences were found in OAR DVHs between patients with and without GI and GU toxicities. No grade 3/4 toxicities were reported. CONCLUSION: The empty bladder preparation approach has non-inferior acute and intermediate post RT GI and GU toxicities in patients treated for localised prostate cancer with advanced radiotherapy techniques compared to the full bladder preparation.
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spelling pubmed-70337952020-02-24 The impact of bladder preparation protocols on post treatment toxicity in radiotherapy for localised prostate cancer patients Tsang, Yat Man Hoskin, Peter Tech Innov Patient Support Radiat Oncol Short communications and technical note OBJECTIVE: This study compares the post radiotherapy related toxicity between the use of an empty and a full bladder preparation protocol in patients receiving radical radiotherapy for localised prostate cancer. METHODS AND MATERIALS: A retrospective review of patient treatment records in which they were treated with a standard radiotherapy schedule (60Gy/20 fractions) to prostates and base of seminal vesicles only and followed two different bladder preparation (empty and full) protocols was carried out. This included each patient's daily image guided radiotherapy (IGRT) setup, treatment time, bladder size on planning computed tomography, organs at risk dose volume histograms (OAR DVHs) and 12 months post treatment gastrointestinal (GI) and genitourinary (GU) toxicity data. RESULTS: 20 patients were included. There were significant differences in IGRT setup between the two groups. Although treatment times of the two groups were not significantly different, 5/200 (2.5%) sessions were longer than 20 min in the full bladder group while this was not found in the other group. Associations between bladder preparation protocols and GI (p = 1.0) and GU (p = 0.6) toxicities were not statistically significant. The bladder size on planning CT was not significantly correlated to the GI (R = 0.06, p = 0.8) or GU (R = 0.27, p = 0.3) toxicity scores. No significant differences were found in OAR DVHs between patients with and without GI and GU toxicities. No grade 3/4 toxicities were reported. CONCLUSION: The empty bladder preparation approach has non-inferior acute and intermediate post RT GI and GU toxicities in patients treated for localised prostate cancer with advanced radiotherapy techniques compared to the full bladder preparation. Elsevier 2017-11-02 /pmc/articles/PMC7033795/ /pubmed/32095565 http://dx.doi.org/10.1016/j.tipsro.2017.10.001 Text en Crown Copyright © 2017 Published by Elsevier Ireland Ltd on behalf of European Society for Radiotherapy & Oncology. http://creativecommons.org/licenses/by-nc-nd/4.0/ This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Short communications and technical note
Tsang, Yat Man
Hoskin, Peter
The impact of bladder preparation protocols on post treatment toxicity in radiotherapy for localised prostate cancer patients
title The impact of bladder preparation protocols on post treatment toxicity in radiotherapy for localised prostate cancer patients
title_full The impact of bladder preparation protocols on post treatment toxicity in radiotherapy for localised prostate cancer patients
title_fullStr The impact of bladder preparation protocols on post treatment toxicity in radiotherapy for localised prostate cancer patients
title_full_unstemmed The impact of bladder preparation protocols on post treatment toxicity in radiotherapy for localised prostate cancer patients
title_short The impact of bladder preparation protocols on post treatment toxicity in radiotherapy for localised prostate cancer patients
title_sort impact of bladder preparation protocols on post treatment toxicity in radiotherapy for localised prostate cancer patients
topic Short communications and technical note
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7033795/
https://www.ncbi.nlm.nih.gov/pubmed/32095565
http://dx.doi.org/10.1016/j.tipsro.2017.10.001
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