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Effects of bladder distension on dose distribution of vaginal vault brachytherapy in patients with endometrial cancer
PURPOSE: To investigate dosimetric effects of bladder distention on organs at risk (OARs) during treatment of endometrial cancer using 3D image-based planning of postoperative vaginal vault brachytherapy (BRT). MATERIAL AND METHODS: Fifteen patients with early-stage endometrial cancer were studied,...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Termedia Publishing House
2014
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4300363/ https://www.ncbi.nlm.nih.gov/pubmed/25834581 http://dx.doi.org/10.5114/jcb.2014.47868 |
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author | Guler, Ozan C. Onal, Cem Acibuci, Ibrahim |
author_facet | Guler, Ozan C. Onal, Cem Acibuci, Ibrahim |
author_sort | Guler, Ozan C. |
collection | PubMed |
description | PURPOSE: To investigate dosimetric effects of bladder distention on organs at risk (OARs) during treatment of endometrial cancer using 3D image-based planning of postoperative vaginal vault brachytherapy (BRT). MATERIAL AND METHODS: Fifteen patients with early-stage endometrial cancer were studied, each undergoing adjuvant BRT of vaginal vault via 3.5 cm diameter cylinder. As treatment, 25 Gy in 5 fractions were delivered to 5 mm depth of the vaginal mucosa. Dose-volume histograms of OARs were generated individually with bladder empty and with bladder inflated by sterile saline (180 ml), to compare doses received. RESULTS: Bladder distention appreciably impacted dosimetry of bladder, sigmoid colon, and small bowel, but dosimetry of rectum was unaffected. With bladder inflated, mean cylinder-to-bowel distance increased significantly (1.69 cm vs. 1.20 cm; p = 0.006). Mean minimum dose to most exposed 2 cc (D(2cc)) volume also rose significantly at bladder (5.40 Gy vs. 4.55 Gy [18.7%]; p < 0.001), as opposed to near-significant reductions in D(2cc) at sigmoid colon (15.1%; p = 0.11) and at small bowel (10.5%; p = 0.14). A full bladder had no effect on dose to 50% volume (D(50%)) of bladder or rectum, and declines seen in mean D(50%) values of sigmoid colon (22.7%; p = 0.12) and small bowel (19.0%; p = 0.13) again fell short of statistical significance. CONCLUSIONS: The combination of a full bladder and an empty rectum may cause significant unwanted increases in BRT dosing of bladder, without significantly impacting sigmoid colon and small bowel exposures. These findings should be validated through further clinical studies. |
format | Online Article Text |
id | pubmed-4300363 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | Termedia Publishing House |
record_format | MEDLINE/PubMed |
spelling | pubmed-43003632015-04-01 Effects of bladder distension on dose distribution of vaginal vault brachytherapy in patients with endometrial cancer Guler, Ozan C. Onal, Cem Acibuci, Ibrahim J Contemp Brachytherapy Original Paper PURPOSE: To investigate dosimetric effects of bladder distention on organs at risk (OARs) during treatment of endometrial cancer using 3D image-based planning of postoperative vaginal vault brachytherapy (BRT). MATERIAL AND METHODS: Fifteen patients with early-stage endometrial cancer were studied, each undergoing adjuvant BRT of vaginal vault via 3.5 cm diameter cylinder. As treatment, 25 Gy in 5 fractions were delivered to 5 mm depth of the vaginal mucosa. Dose-volume histograms of OARs were generated individually with bladder empty and with bladder inflated by sterile saline (180 ml), to compare doses received. RESULTS: Bladder distention appreciably impacted dosimetry of bladder, sigmoid colon, and small bowel, but dosimetry of rectum was unaffected. With bladder inflated, mean cylinder-to-bowel distance increased significantly (1.69 cm vs. 1.20 cm; p = 0.006). Mean minimum dose to most exposed 2 cc (D(2cc)) volume also rose significantly at bladder (5.40 Gy vs. 4.55 Gy [18.7%]; p < 0.001), as opposed to near-significant reductions in D(2cc) at sigmoid colon (15.1%; p = 0.11) and at small bowel (10.5%; p = 0.14). A full bladder had no effect on dose to 50% volume (D(50%)) of bladder or rectum, and declines seen in mean D(50%) values of sigmoid colon (22.7%; p = 0.12) and small bowel (19.0%; p = 0.13) again fell short of statistical significance. CONCLUSIONS: The combination of a full bladder and an empty rectum may cause significant unwanted increases in BRT dosing of bladder, without significantly impacting sigmoid colon and small bowel exposures. These findings should be validated through further clinical studies. Termedia Publishing House 2014-12-31 2015-01 /pmc/articles/PMC4300363/ /pubmed/25834581 http://dx.doi.org/10.5114/jcb.2014.47868 Text en Copyright © 2014 Termedia http://creativecommons.org/licenses/by-nc-nd/3.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution-Noncommercial 3.0 Unported License, permitting all non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Original Paper Guler, Ozan C. Onal, Cem Acibuci, Ibrahim Effects of bladder distension on dose distribution of vaginal vault brachytherapy in patients with endometrial cancer |
title | Effects of bladder distension on dose distribution of vaginal vault brachytherapy in patients with endometrial cancer |
title_full | Effects of bladder distension on dose distribution of vaginal vault brachytherapy in patients with endometrial cancer |
title_fullStr | Effects of bladder distension on dose distribution of vaginal vault brachytherapy in patients with endometrial cancer |
title_full_unstemmed | Effects of bladder distension on dose distribution of vaginal vault brachytherapy in patients with endometrial cancer |
title_short | Effects of bladder distension on dose distribution of vaginal vault brachytherapy in patients with endometrial cancer |
title_sort | effects of bladder distension on dose distribution of vaginal vault brachytherapy in patients with endometrial cancer |
topic | Original Paper |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4300363/ https://www.ncbi.nlm.nih.gov/pubmed/25834581 http://dx.doi.org/10.5114/jcb.2014.47868 |
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