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The curative effect of androgen deprivation therapy alone is insufficient in high-risk prostate cancer

To compare the outcomes of patients with high-risk prostate cancer treated by primary radical prostatectomy (RP) and primary androgen deprivation therapy (ADT). The study included patients with high-risk or very high-risk prostate cancer. Patients treated with definitive radiation therapy and those...

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Autores principales: Choi, Se Young, Lim, Bumjin, Chi, Byung Hoon, Lee, Wonchul, Kim, Jung Hoon, Kyung, Yoon Soo, You, Dalsan, Kim, Choung-Soo
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Lippincott Williams & Wilkins 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8341274/
https://www.ncbi.nlm.nih.gov/pubmed/34397848
http://dx.doi.org/10.1097/MD.0000000000026833
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author Choi, Se Young
Lim, Bumjin
Chi, Byung Hoon
Lee, Wonchul
Kim, Jung Hoon
Kyung, Yoon Soo
You, Dalsan
Kim, Choung-Soo
author_facet Choi, Se Young
Lim, Bumjin
Chi, Byung Hoon
Lee, Wonchul
Kim, Jung Hoon
Kyung, Yoon Soo
You, Dalsan
Kim, Choung-Soo
author_sort Choi, Se Young
collection PubMed
description To compare the outcomes of patients with high-risk prostate cancer treated by primary radical prostatectomy (RP) and primary androgen deprivation therapy (ADT). The study included patients with high-risk or very high-risk prostate cancer. Patients treated with definitive radiation therapy and those with clinical N1 and M1 disease were excluded. The RP group was divided into sub-cohorts of patients treated with ADT and those who received ADT after biochemical recurrence post-RP. Cancer-specific survival (CSS) and overall survival (OS) were analyzed using the Kaplan–Meier method and the Cox proportional hazards model. The study analyzed 859 patients divided into the RP group (n = 654) and ADT group (n = 205). Castration-resistant prostate cancer was detected in 23 (3.5%) patients in the RP group and 43 (21.0%) patients in the ADT group. Mortality cases included 63 (9.6%) patients in the RP group and 91 (44.4%) patients in the ADT group. CSS (P = .0002) and OS (P < .0001) were significantly higher in the RP group than in the ADT group. In the sub-cohort, CSS did not differ significantly between the RP and ADT groups, whereas OS was significantly higher in the RP group than in the ADT group (P < .0001). In the multivariate analysis, primary ADT increased CSS (hazard ratio, 2.068; P = .0498) and OS (hazard ratio, 3.218; P < .0001) compared with RP. In clinically localized high-risk prostate cancer patients, primary RP was associated with better CSS and OS than primary ADT. Comprehensive counseling in this cohort of patients will help the selection of treatment.
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spelling pubmed-83412742021-08-07 The curative effect of androgen deprivation therapy alone is insufficient in high-risk prostate cancer Choi, Se Young Lim, Bumjin Chi, Byung Hoon Lee, Wonchul Kim, Jung Hoon Kyung, Yoon Soo You, Dalsan Kim, Choung-Soo Medicine (Baltimore) 7300 To compare the outcomes of patients with high-risk prostate cancer treated by primary radical prostatectomy (RP) and primary androgen deprivation therapy (ADT). The study included patients with high-risk or very high-risk prostate cancer. Patients treated with definitive radiation therapy and those with clinical N1 and M1 disease were excluded. The RP group was divided into sub-cohorts of patients treated with ADT and those who received ADT after biochemical recurrence post-RP. Cancer-specific survival (CSS) and overall survival (OS) were analyzed using the Kaplan–Meier method and the Cox proportional hazards model. The study analyzed 859 patients divided into the RP group (n = 654) and ADT group (n = 205). Castration-resistant prostate cancer was detected in 23 (3.5%) patients in the RP group and 43 (21.0%) patients in the ADT group. Mortality cases included 63 (9.6%) patients in the RP group and 91 (44.4%) patients in the ADT group. CSS (P = .0002) and OS (P < .0001) were significantly higher in the RP group than in the ADT group. In the sub-cohort, CSS did not differ significantly between the RP and ADT groups, whereas OS was significantly higher in the RP group than in the ADT group (P < .0001). In the multivariate analysis, primary ADT increased CSS (hazard ratio, 2.068; P = .0498) and OS (hazard ratio, 3.218; P < .0001) compared with RP. In clinically localized high-risk prostate cancer patients, primary RP was associated with better CSS and OS than primary ADT. Comprehensive counseling in this cohort of patients will help the selection of treatment. Lippincott Williams & Wilkins 2021-08-06 /pmc/articles/PMC8341274/ /pubmed/34397848 http://dx.doi.org/10.1097/MD.0000000000026833 Text en Copyright © 2021 the Author(s). Published by Wolters Kluwer Health, Inc. 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 License 4.0 (CCBY-NC), where it is permissible to download, share, remix, transform, and buildup the work provided it is properly cited. The work cannot be used commercially without permission from the journal. http://creativecommons.org/licenses/by-nc/4.0 (https://creativecommons.org/licenses/by-nc/4.0/)
spellingShingle 7300
Choi, Se Young
Lim, Bumjin
Chi, Byung Hoon
Lee, Wonchul
Kim, Jung Hoon
Kyung, Yoon Soo
You, Dalsan
Kim, Choung-Soo
The curative effect of androgen deprivation therapy alone is insufficient in high-risk prostate cancer
title The curative effect of androgen deprivation therapy alone is insufficient in high-risk prostate cancer
title_full The curative effect of androgen deprivation therapy alone is insufficient in high-risk prostate cancer
title_fullStr The curative effect of androgen deprivation therapy alone is insufficient in high-risk prostate cancer
title_full_unstemmed The curative effect of androgen deprivation therapy alone is insufficient in high-risk prostate cancer
title_short The curative effect of androgen deprivation therapy alone is insufficient in high-risk prostate cancer
title_sort curative effect of androgen deprivation therapy alone is insufficient in high-risk prostate cancer
topic 7300
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8341274/
https://www.ncbi.nlm.nih.gov/pubmed/34397848
http://dx.doi.org/10.1097/MD.0000000000026833
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