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Impact of androgen-deprivation therapy on the outcome of dose-escalation prostate cancer radiotherapy without elective pelvic irradiation

The benefit of androgen-deprivation therapy (ADT) in combination with dose-escalated radiotherapy (DERT) for localized prostate cancer has not been determined in randomized studies. In this study, the benefit of ADT was assessed in patients uniformly treated with dose-escalated intensity-modulated r...

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Autores principales: Hou, Wei-Hsien, Huang, Chao-Yuan, Wang, Chia-Chun, Lan, Keng-Hsueh, Chen, Chung-Hsin, Yu, Hong-Jen, Liu, Shih-Ping, Lai, Ming-Kuen, Pu, Yeong-Shau, Cheng, Jason Chia-Hsien
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Medknow Publications & Media Pvt Ltd 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5566856/
https://www.ncbi.nlm.nih.gov/pubmed/27506334
http://dx.doi.org/10.4103/1008-682X.183569
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author Hou, Wei-Hsien
Huang, Chao-Yuan
Wang, Chia-Chun
Lan, Keng-Hsueh
Chen, Chung-Hsin
Yu, Hong-Jen
Liu, Shih-Ping
Lai, Ming-Kuen
Pu, Yeong-Shau
Cheng, Jason Chia-Hsien
author_facet Hou, Wei-Hsien
Huang, Chao-Yuan
Wang, Chia-Chun
Lan, Keng-Hsueh
Chen, Chung-Hsin
Yu, Hong-Jen
Liu, Shih-Ping
Lai, Ming-Kuen
Pu, Yeong-Shau
Cheng, Jason Chia-Hsien
author_sort Hou, Wei-Hsien
collection PubMed
description The benefit of androgen-deprivation therapy (ADT) in combination with dose-escalated radiotherapy (DERT) for localized prostate cancer has not been determined in randomized studies. In this study, the benefit of ADT was assessed in patients uniformly treated with dose-escalated intensity-modulated radiation therapy (IMRT) to the prostate and seminal vesicles but not pelvis. In all, 419 patients with localized prostate adenocarcinoma underwent definitive IMRT (cumulative dose 78 Gy), with 32.6%, 33.1%, 32.1%, and 2.1% having T1 through T4 disease, respectively, and 51.2% having high-risk disease. ADT was given to 76.1% of patients. With a median follow-up of 60 months, 5-year biochemical failure-free, disease-free, and overall survival rates were 87%, 86%, and 87%, respectively. T stage was an independent predictor of all three rates. Five-year pelvic nodal recurrence rate was 2.9%. ADT improved biochemical failure-free and disease-free survival but not overall survival. ADT showed benefit in high-risk disease but not intermediate-risk disease. Late gastrointestinal and genitourinary toxicities ≥ grade 2 occurred in 11.0% and 6.7%, respectively. In conclusion, DERT with 78 Gy yields good disease control and low rate of pelvic nodal recurrence. ADT improves disease-free survival in patients with high-risk but not intermediate-risk disease.
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spelling pubmed-55668562017-09-02 Impact of androgen-deprivation therapy on the outcome of dose-escalation prostate cancer radiotherapy without elective pelvic irradiation Hou, Wei-Hsien Huang, Chao-Yuan Wang, Chia-Chun Lan, Keng-Hsueh Chen, Chung-Hsin Yu, Hong-Jen Liu, Shih-Ping Lai, Ming-Kuen Pu, Yeong-Shau Cheng, Jason Chia-Hsien Asian J Androl Original Article The benefit of androgen-deprivation therapy (ADT) in combination with dose-escalated radiotherapy (DERT) for localized prostate cancer has not been determined in randomized studies. In this study, the benefit of ADT was assessed in patients uniformly treated with dose-escalated intensity-modulated radiation therapy (IMRT) to the prostate and seminal vesicles but not pelvis. In all, 419 patients with localized prostate adenocarcinoma underwent definitive IMRT (cumulative dose 78 Gy), with 32.6%, 33.1%, 32.1%, and 2.1% having T1 through T4 disease, respectively, and 51.2% having high-risk disease. ADT was given to 76.1% of patients. With a median follow-up of 60 months, 5-year biochemical failure-free, disease-free, and overall survival rates were 87%, 86%, and 87%, respectively. T stage was an independent predictor of all three rates. Five-year pelvic nodal recurrence rate was 2.9%. ADT improved biochemical failure-free and disease-free survival but not overall survival. ADT showed benefit in high-risk disease but not intermediate-risk disease. Late gastrointestinal and genitourinary toxicities ≥ grade 2 occurred in 11.0% and 6.7%, respectively. In conclusion, DERT with 78 Gy yields good disease control and low rate of pelvic nodal recurrence. ADT improves disease-free survival in patients with high-risk but not intermediate-risk disease. Medknow Publications & Media Pvt Ltd 2017 2016-07-29 /pmc/articles/PMC5566856/ /pubmed/27506334 http://dx.doi.org/10.4103/1008-682X.183569 Text en Copyright: © The Author(s)(2017) http://creativecommons.org/licenses/by-nc-sa/3.0 This is an open access article distributed under the terms of the Creative Commons Attribution-NonCommercial-ShareAlike 3.0 License, which allows others to remix, tweak, and build upon the work non-commercially, as long as the author is credited and the new creations are licensed under the identical terms.
spellingShingle Original Article
Hou, Wei-Hsien
Huang, Chao-Yuan
Wang, Chia-Chun
Lan, Keng-Hsueh
Chen, Chung-Hsin
Yu, Hong-Jen
Liu, Shih-Ping
Lai, Ming-Kuen
Pu, Yeong-Shau
Cheng, Jason Chia-Hsien
Impact of androgen-deprivation therapy on the outcome of dose-escalation prostate cancer radiotherapy without elective pelvic irradiation
title Impact of androgen-deprivation therapy on the outcome of dose-escalation prostate cancer radiotherapy without elective pelvic irradiation
title_full Impact of androgen-deprivation therapy on the outcome of dose-escalation prostate cancer radiotherapy without elective pelvic irradiation
title_fullStr Impact of androgen-deprivation therapy on the outcome of dose-escalation prostate cancer radiotherapy without elective pelvic irradiation
title_full_unstemmed Impact of androgen-deprivation therapy on the outcome of dose-escalation prostate cancer radiotherapy without elective pelvic irradiation
title_short Impact of androgen-deprivation therapy on the outcome of dose-escalation prostate cancer radiotherapy without elective pelvic irradiation
title_sort impact of androgen-deprivation therapy on the outcome of dose-escalation prostate cancer radiotherapy without elective pelvic irradiation
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5566856/
https://www.ncbi.nlm.nih.gov/pubmed/27506334
http://dx.doi.org/10.4103/1008-682X.183569
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