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Evaluation of the effect of prostate volume change on tumor control probability in LDR brachytherapy
PURPOSE: This study evaluates low dose-rate brachytherapy (LDR) prostate plans to determine the biological effect of dose degradation due to prostate volume changes. MATERIAL AND METHODS: In this study, 39 patients were evaluated. Pre-implant prostate volume was determined using ultrasound. These im...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Termedia Publishing House
2011
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3551355/ https://www.ncbi.nlm.nih.gov/pubmed/23346121 http://dx.doi.org/10.5114/jcb.2011.24818 |
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author | Knaup, Courtney Mavroidis, Panayiotis Stathakis, Sotirios Smith, Mark Swanson, Gregory Papanikolaou, Niko |
author_facet | Knaup, Courtney Mavroidis, Panayiotis Stathakis, Sotirios Smith, Mark Swanson, Gregory Papanikolaou, Niko |
author_sort | Knaup, Courtney |
collection | PubMed |
description | PURPOSE: This study evaluates low dose-rate brachytherapy (LDR) prostate plans to determine the biological effect of dose degradation due to prostate volume changes. MATERIAL AND METHODS: In this study, 39 patients were evaluated. Pre-implant prostate volume was determined using ultrasound. These images were used with the treatment planning system (Nucletron Spot Pro 3.1(®)) to create treatment plans using (103)Pd seeds. Following the implant, patients were imaged using CT for post-implant dosimetry. From the pre and post-implant DVHs, the biologically equivalent dose and the tumor control probability (TCP) were determined using the biologically effective uniform dose. The model used RBE = 1.75 and α/β = 2 Gy. RESULTS: The prostate volume changed between pre and post implant image sets ranged from –8% to 110%. TCP and the mean dose were reduced up to 21% and 56%, respectively. TCP is observed to decrease as the mean dose decreases to the prostate. The post-implant tumor dose was generally observed to decrease, compared to the planned dose. A critical uniform dose of 130 Gy was established. Below this dose, TCP begins to fall-off. It was also determined that patients with a small prostates were more likely to suffer TCP decrease. CONCLUSIONS: The biological effect of post operative prostate growth due to operative trauma in LDR was evaluated using the concept. The post-implant dose was lower than the planned dose due to an increase of prostate volume post-implant. A critical uniform dose of 130 Gy was determined, below which TCP begun to decline. |
format | Online Article Text |
id | pubmed-3551355 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2011 |
publisher | Termedia Publishing House |
record_format | MEDLINE/PubMed |
spelling | pubmed-35513552013-01-23 Evaluation of the effect of prostate volume change on tumor control probability in LDR brachytherapy Knaup, Courtney Mavroidis, Panayiotis Stathakis, Sotirios Smith, Mark Swanson, Gregory Papanikolaou, Niko J Contemp Brachytherapy Original Article PURPOSE: This study evaluates low dose-rate brachytherapy (LDR) prostate plans to determine the biological effect of dose degradation due to prostate volume changes. MATERIAL AND METHODS: In this study, 39 patients were evaluated. Pre-implant prostate volume was determined using ultrasound. These images were used with the treatment planning system (Nucletron Spot Pro 3.1(®)) to create treatment plans using (103)Pd seeds. Following the implant, patients were imaged using CT for post-implant dosimetry. From the pre and post-implant DVHs, the biologically equivalent dose and the tumor control probability (TCP) were determined using the biologically effective uniform dose. The model used RBE = 1.75 and α/β = 2 Gy. RESULTS: The prostate volume changed between pre and post implant image sets ranged from –8% to 110%. TCP and the mean dose were reduced up to 21% and 56%, respectively. TCP is observed to decrease as the mean dose decreases to the prostate. The post-implant tumor dose was generally observed to decrease, compared to the planned dose. A critical uniform dose of 130 Gy was established. Below this dose, TCP begins to fall-off. It was also determined that patients with a small prostates were more likely to suffer TCP decrease. CONCLUSIONS: The biological effect of post operative prostate growth due to operative trauma in LDR was evaluated using the concept. The post-implant dose was lower than the planned dose due to an increase of prostate volume post-implant. A critical uniform dose of 130 Gy was determined, below which TCP begun to decline. Termedia Publishing House 2011-09-30 2011-09 /pmc/articles/PMC3551355/ /pubmed/23346121 http://dx.doi.org/10.5114/jcb.2011.24818 Text en Copyright © 2011 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 Article Knaup, Courtney Mavroidis, Panayiotis Stathakis, Sotirios Smith, Mark Swanson, Gregory Papanikolaou, Niko Evaluation of the effect of prostate volume change on tumor control probability in LDR brachytherapy |
title | Evaluation of the effect of prostate volume change on tumor control probability in LDR brachytherapy |
title_full | Evaluation of the effect of prostate volume change on tumor control probability in LDR brachytherapy |
title_fullStr | Evaluation of the effect of prostate volume change on tumor control probability in LDR brachytherapy |
title_full_unstemmed | Evaluation of the effect of prostate volume change on tumor control probability in LDR brachytherapy |
title_short | Evaluation of the effect of prostate volume change on tumor control probability in LDR brachytherapy |
title_sort | evaluation of the effect of prostate volume change on tumor control probability in ldr brachytherapy |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3551355/ https://www.ncbi.nlm.nih.gov/pubmed/23346121 http://dx.doi.org/10.5114/jcb.2011.24818 |
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