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Impacts of androgen deprivation therapy on the risks and outcomes of SARS-CoV-2 infection in patients with prostate cancer

Studies have investigated the effects of androgen deprivation therapy (ADT) use on the incidence and clinical outcomes of coronavirus disease 2019 (COVID-19); however, the results have been inconsistent. We searched the PubMed, Medline, Cochrane, Scopus, and Web of Science databases from inception t...

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Autores principales: Huang, Yuan-Bin, Li, Wei-Lin, Sun, Man, Duan, Xu, Wang, Yu-Tong, Zhang, Lu-Xin, Xin, Zi-Han, Yun, Zhi-Fei, Fan, Bo, Li, Xian-Cheng
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Wolters Kluwer - Medknow 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10226495/
https://www.ncbi.nlm.nih.gov/pubmed/35915542
http://dx.doi.org/10.4103/aja202246
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author Huang, Yuan-Bin
Li, Wei-Lin
Sun, Man
Duan, Xu
Wang, Yu-Tong
Zhang, Lu-Xin
Xin, Zi-Han
Yun, Zhi-Fei
Fan, Bo
Li, Xian-Cheng
author_facet Huang, Yuan-Bin
Li, Wei-Lin
Sun, Man
Duan, Xu
Wang, Yu-Tong
Zhang, Lu-Xin
Xin, Zi-Han
Yun, Zhi-Fei
Fan, Bo
Li, Xian-Cheng
author_sort Huang, Yuan-Bin
collection PubMed
description Studies have investigated the effects of androgen deprivation therapy (ADT) use on the incidence and clinical outcomes of coronavirus disease 2019 (COVID-19); however, the results have been inconsistent. We searched the PubMed, Medline, Cochrane, Scopus, and Web of Science databases from inception to March 2022; 13 studies covering 84 003 prostate cancer (PCa) patients with or without ADT met the eligibility criteria and were included in the meta-analysis. We calculated the pooled risk ratios (RRs) with 95% confidence intervals (CIs) to explore the association between ADT use and the infection risk of severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) and severity of COVID-19. After synthesizing the evidence, the pooled RR in the SARS-CoV-2 positive group was equal to 1.17, and the SARS-CoV-2 positive risk in PCa patients using ADT was not significantly different from that in those not using ADT (P = 0.544). Moreover, no significant results concerning the beneficial effect of ADT on the rate of intensive care unit admission (RR = 1.04, P = 0.872) or death risk (RR = 1.23, P = 0.53) were found. However, PCa patients with a history of ADT use had a markedly higher COVID-19 hospitalization rate (RR = 1.31, P = 0.015) than those with no history of ADT use. These findings indicate that ADT use by PCa patients is associated with a high risk of hospitalization during infection with SARS-CoV-2. A large number of high quality studies are needed to confirm these results.
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spelling pubmed-102264952023-05-30 Impacts of androgen deprivation therapy on the risks and outcomes of SARS-CoV-2 infection in patients with prostate cancer Huang, Yuan-Bin Li, Wei-Lin Sun, Man Duan, Xu Wang, Yu-Tong Zhang, Lu-Xin Xin, Zi-Han Yun, Zhi-Fei Fan, Bo Li, Xian-Cheng Asian J Androl Original Article Studies have investigated the effects of androgen deprivation therapy (ADT) use on the incidence and clinical outcomes of coronavirus disease 2019 (COVID-19); however, the results have been inconsistent. We searched the PubMed, Medline, Cochrane, Scopus, and Web of Science databases from inception to March 2022; 13 studies covering 84 003 prostate cancer (PCa) patients with or without ADT met the eligibility criteria and were included in the meta-analysis. We calculated the pooled risk ratios (RRs) with 95% confidence intervals (CIs) to explore the association between ADT use and the infection risk of severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) and severity of COVID-19. After synthesizing the evidence, the pooled RR in the SARS-CoV-2 positive group was equal to 1.17, and the SARS-CoV-2 positive risk in PCa patients using ADT was not significantly different from that in those not using ADT (P = 0.544). Moreover, no significant results concerning the beneficial effect of ADT on the rate of intensive care unit admission (RR = 1.04, P = 0.872) or death risk (RR = 1.23, P = 0.53) were found. However, PCa patients with a history of ADT use had a markedly higher COVID-19 hospitalization rate (RR = 1.31, P = 0.015) than those with no history of ADT use. These findings indicate that ADT use by PCa patients is associated with a high risk of hospitalization during infection with SARS-CoV-2. A large number of high quality studies are needed to confirm these results. Wolters Kluwer - Medknow 2022-07-29 /pmc/articles/PMC10226495/ /pubmed/35915542 http://dx.doi.org/10.4103/aja202246 Text en Copyright: © The Author(s)(2022) https://creativecommons.org/licenses/by-nc-sa/4.0/This is an open access journal, and articles are distributed under the terms of the Creative Commons Attribution-NonCommercial-ShareAlike 4.0 License, which allows others to remix, tweak, and build upon the work non-commercially, as long as appropriate credit is given and the new creations are licensed under the identical terms.
spellingShingle Original Article
Huang, Yuan-Bin
Li, Wei-Lin
Sun, Man
Duan, Xu
Wang, Yu-Tong
Zhang, Lu-Xin
Xin, Zi-Han
Yun, Zhi-Fei
Fan, Bo
Li, Xian-Cheng
Impacts of androgen deprivation therapy on the risks and outcomes of SARS-CoV-2 infection in patients with prostate cancer
title Impacts of androgen deprivation therapy on the risks and outcomes of SARS-CoV-2 infection in patients with prostate cancer
title_full Impacts of androgen deprivation therapy on the risks and outcomes of SARS-CoV-2 infection in patients with prostate cancer
title_fullStr Impacts of androgen deprivation therapy on the risks and outcomes of SARS-CoV-2 infection in patients with prostate cancer
title_full_unstemmed Impacts of androgen deprivation therapy on the risks and outcomes of SARS-CoV-2 infection in patients with prostate cancer
title_short Impacts of androgen deprivation therapy on the risks and outcomes of SARS-CoV-2 infection in patients with prostate cancer
title_sort impacts of androgen deprivation therapy on the risks and outcomes of sars-cov-2 infection in patients with prostate cancer
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10226495/
https://www.ncbi.nlm.nih.gov/pubmed/35915542
http://dx.doi.org/10.4103/aja202246
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