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Is neoadjuvant androgen deprivation therapy beneficial in prostate cancer treated with definitive radiotherapy?
PURPOSE: To determine whether neoadjuvant androgen deprivation therapy (NADT) improves clinical outcomes in patients with prostate cancer treated with definitive radiotherapy. MATERIALS AND METHODS: We retrospectively reviewed medical records of 201 patients with prostate cancer treated with radioth...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
The Korean Society for Radiation Oncology
2014
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4282999/ https://www.ncbi.nlm.nih.gov/pubmed/25568853 http://dx.doi.org/10.3857/roj.2014.32.4.247 |
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author | Eom, Keun-Yong Ha, Sung W Lee, Eunsik Kwak, Cheol Lee, Sang Eun |
author_facet | Eom, Keun-Yong Ha, Sung W Lee, Eunsik Kwak, Cheol Lee, Sang Eun |
author_sort | Eom, Keun-Yong |
collection | PubMed |
description | PURPOSE: To determine whether neoadjuvant androgen deprivation therapy (NADT) improves clinical outcomes in patients with prostate cancer treated with definitive radiotherapy. MATERIALS AND METHODS: We retrospectively reviewed medical records of 201 patients with prostate cancer treated with radiotherapy between January 1991 and December 2008. Of these, 156 patients with more than 3 years of follow-up were the subjects of this study. The median duration of follow-up was 91.2 months. NADT was given in 103 patients (66%) with median duration of 3.3 months (range, 1.0 to 7.7 months). Radiation dose was escalated gradually from 64 Gy to 81 Gy using intensity-modulated radiotherapy technique. RESULTS: Biochemical relapse-free survival (BCRFS) and overall survival (OS) of all patients were 72.6% and 90.7% at 5 years, respectively. BCRFS and OS of NADT group were 79.5% and 89.8% at 5 years and those of radiotherapy alone group were 58.8% and 92.3% at 5 years, respectively. Risk group (p = 0.010) and radiation dose ≥70 Gy (p = 0.017) affected BCRFS independently. NADT was a significant prognostic factor in univariate analysis, but not in multivariate analysis (p = 0.073). Radiation dose ≥70 Gy was only an independent factor for OS (p = 0.007; hazard ratio, 0.261; 95% confidence interval, 0.071-0.963). CONCLUSION: NADT prior to definitive radiotherapy did not result in significant benefit in terms of BCRFS and OS. NADT should not be performed routinely in the era of dose-escalated radiotherapy. |
format | Online Article Text |
id | pubmed-4282999 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | The Korean Society for Radiation Oncology |
record_format | MEDLINE/PubMed |
spelling | pubmed-42829992015-01-07 Is neoadjuvant androgen deprivation therapy beneficial in prostate cancer treated with definitive radiotherapy? Eom, Keun-Yong Ha, Sung W Lee, Eunsik Kwak, Cheol Lee, Sang Eun Radiat Oncol J Original Article PURPOSE: To determine whether neoadjuvant androgen deprivation therapy (NADT) improves clinical outcomes in patients with prostate cancer treated with definitive radiotherapy. MATERIALS AND METHODS: We retrospectively reviewed medical records of 201 patients with prostate cancer treated with radiotherapy between January 1991 and December 2008. Of these, 156 patients with more than 3 years of follow-up were the subjects of this study. The median duration of follow-up was 91.2 months. NADT was given in 103 patients (66%) with median duration of 3.3 months (range, 1.0 to 7.7 months). Radiation dose was escalated gradually from 64 Gy to 81 Gy using intensity-modulated radiotherapy technique. RESULTS: Biochemical relapse-free survival (BCRFS) and overall survival (OS) of all patients were 72.6% and 90.7% at 5 years, respectively. BCRFS and OS of NADT group were 79.5% and 89.8% at 5 years and those of radiotherapy alone group were 58.8% and 92.3% at 5 years, respectively. Risk group (p = 0.010) and radiation dose ≥70 Gy (p = 0.017) affected BCRFS independently. NADT was a significant prognostic factor in univariate analysis, but not in multivariate analysis (p = 0.073). Radiation dose ≥70 Gy was only an independent factor for OS (p = 0.007; hazard ratio, 0.261; 95% confidence interval, 0.071-0.963). CONCLUSION: NADT prior to definitive radiotherapy did not result in significant benefit in terms of BCRFS and OS. NADT should not be performed routinely in the era of dose-escalated radiotherapy. The Korean Society for Radiation Oncology 2014-12 2014-12-30 /pmc/articles/PMC4282999/ /pubmed/25568853 http://dx.doi.org/10.3857/roj.2014.32.4.247 Text en Copyright © 2014. The Korean Society for Radiation Oncology http://creativecommons.org/licenses/by-nc/3.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/3.0/) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Original Article Eom, Keun-Yong Ha, Sung W Lee, Eunsik Kwak, Cheol Lee, Sang Eun Is neoadjuvant androgen deprivation therapy beneficial in prostate cancer treated with definitive radiotherapy? |
title | Is neoadjuvant androgen deprivation therapy beneficial in prostate cancer treated with definitive radiotherapy? |
title_full | Is neoadjuvant androgen deprivation therapy beneficial in prostate cancer treated with definitive radiotherapy? |
title_fullStr | Is neoadjuvant androgen deprivation therapy beneficial in prostate cancer treated with definitive radiotherapy? |
title_full_unstemmed | Is neoadjuvant androgen deprivation therapy beneficial in prostate cancer treated with definitive radiotherapy? |
title_short | Is neoadjuvant androgen deprivation therapy beneficial in prostate cancer treated with definitive radiotherapy? |
title_sort | is neoadjuvant androgen deprivation therapy beneficial in prostate cancer treated with definitive radiotherapy? |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4282999/ https://www.ncbi.nlm.nih.gov/pubmed/25568853 http://dx.doi.org/10.3857/roj.2014.32.4.247 |
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