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Comparison of chronic gastrointestinal and genitourinary toxicities between brachytherapy and external beam radiotherapy for patients with prostate cancer: A systematic review and meta-analysis

BACKGROUND: [Formula: see text] I BT is an effective radiotherapy for prostate cancer. However, comparison data of GI and GU toxicities between BT, BT [Formula: see text] EBRT, and EBRT-alone patient groups is limited. OBJECTIVE: To define the GI and GU toxicities in prostate cancer to prevent adver...

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Autores principales: Li, Xuanzhe, Shan, Ligang, Wang, Qianqi, Zhai, Huige, Xuan, Yinghua, Yan, Gen
Formato: Online Artículo Texto
Lenguaje:English
Publicado: IOS Press 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10200168/
https://www.ncbi.nlm.nih.gov/pubmed/37066936
http://dx.doi.org/10.3233/THC-236031
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author Li, Xuanzhe
Shan, Ligang
Wang, Qianqi
Zhai, Huige
Xuan, Yinghua
Yan, Gen
author_facet Li, Xuanzhe
Shan, Ligang
Wang, Qianqi
Zhai, Huige
Xuan, Yinghua
Yan, Gen
author_sort Li, Xuanzhe
collection PubMed
description BACKGROUND: [Formula: see text] I BT is an effective radiotherapy for prostate cancer. However, comparison data of GI and GU toxicities between BT, BT [Formula: see text] EBRT, and EBRT-alone patient groups is limited. OBJECTIVE: To define the GI and GU toxicities in prostate cancer to prevent adverse events after treatment. METHODS: We searched published studies in PubMed, Cochrane, and Embase databases up to December 31, 2022. The endpoints were the RRs of GI and GU toxicities. Pooled data were assessed using a random-effects model. RESULTS: Fifteen eligible studies were included into this analysis. LDR-BT had significantly lower RRs than LDR-BT [Formula: see text] EBRT for acute GI (2.13; 95% CI, 1.22–3.69; [Formula: see text] 0.007) and late GI toxicities (3.96; 95% CI, 1.23–12.70; [Formula: see text] 0.02). Moreover, EBRT had significantly higher RRs than LDR-BT for acute GU (2.32; 95% CI, 1.29–4.15; [Formula: see text] 0.005) and late GU toxicities (2.38; 95% CI, 1.27–4.44; [Formula: see text] 0.007). HDR-BT had significantly higher RRs for acute GU toxicities than LDR-BT alone (0.30; 95% CI, 0.23–0.40; [Formula: see text] 0.00001). CONCLUSION: The results implied that BT with and without EBRT can result in both GI and GU toxicities in patients with prostate cancer, with LDR-BT leading to a poorer urinary function than EBRT.
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spelling pubmed-102001682023-05-22 Comparison of chronic gastrointestinal and genitourinary toxicities between brachytherapy and external beam radiotherapy for patients with prostate cancer: A systematic review and meta-analysis Li, Xuanzhe Shan, Ligang Wang, Qianqi Zhai, Huige Xuan, Yinghua Yan, Gen Technol Health Care Review Article BACKGROUND: [Formula: see text] I BT is an effective radiotherapy for prostate cancer. However, comparison data of GI and GU toxicities between BT, BT [Formula: see text] EBRT, and EBRT-alone patient groups is limited. OBJECTIVE: To define the GI and GU toxicities in prostate cancer to prevent adverse events after treatment. METHODS: We searched published studies in PubMed, Cochrane, and Embase databases up to December 31, 2022. The endpoints were the RRs of GI and GU toxicities. Pooled data were assessed using a random-effects model. RESULTS: Fifteen eligible studies were included into this analysis. LDR-BT had significantly lower RRs than LDR-BT [Formula: see text] EBRT for acute GI (2.13; 95% CI, 1.22–3.69; [Formula: see text] 0.007) and late GI toxicities (3.96; 95% CI, 1.23–12.70; [Formula: see text] 0.02). Moreover, EBRT had significantly higher RRs than LDR-BT for acute GU (2.32; 95% CI, 1.29–4.15; [Formula: see text] 0.005) and late GU toxicities (2.38; 95% CI, 1.27–4.44; [Formula: see text] 0.007). HDR-BT had significantly higher RRs for acute GU toxicities than LDR-BT alone (0.30; 95% CI, 0.23–0.40; [Formula: see text] 0.00001). CONCLUSION: The results implied that BT with and without EBRT can result in both GI and GU toxicities in patients with prostate cancer, with LDR-BT leading to a poorer urinary function than EBRT. IOS Press 2023-04-28 /pmc/articles/PMC10200168/ /pubmed/37066936 http://dx.doi.org/10.3233/THC-236031 Text en © 2023 – The authors. Published by IOS Press. https://creativecommons.org/licenses/by-nc/4.0/This is an open access article distributed under the terms of the Creative Commons Attribution Non-Commercial (CC BY-NC 4.0) License (https://creativecommons.org/licenses/by-nc/4.0/) , which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Review Article
Li, Xuanzhe
Shan, Ligang
Wang, Qianqi
Zhai, Huige
Xuan, Yinghua
Yan, Gen
Comparison of chronic gastrointestinal and genitourinary toxicities between brachytherapy and external beam radiotherapy for patients with prostate cancer: A systematic review and meta-analysis
title Comparison of chronic gastrointestinal and genitourinary toxicities between brachytherapy and external beam radiotherapy for patients with prostate cancer: A systematic review and meta-analysis
title_full Comparison of chronic gastrointestinal and genitourinary toxicities between brachytherapy and external beam radiotherapy for patients with prostate cancer: A systematic review and meta-analysis
title_fullStr Comparison of chronic gastrointestinal and genitourinary toxicities between brachytherapy and external beam radiotherapy for patients with prostate cancer: A systematic review and meta-analysis
title_full_unstemmed Comparison of chronic gastrointestinal and genitourinary toxicities between brachytherapy and external beam radiotherapy for patients with prostate cancer: A systematic review and meta-analysis
title_short Comparison of chronic gastrointestinal and genitourinary toxicities between brachytherapy and external beam radiotherapy for patients with prostate cancer: A systematic review and meta-analysis
title_sort comparison of chronic gastrointestinal and genitourinary toxicities between brachytherapy and external beam radiotherapy for patients with prostate cancer: a systematic review and meta-analysis
topic Review Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10200168/
https://www.ncbi.nlm.nih.gov/pubmed/37066936
http://dx.doi.org/10.3233/THC-236031
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