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A Phase 2 Trial of the Effect of Antiandrogen Therapy on COVID-19 Outcome: No Evidence of Benefit, Supported by Epidemiology and In Vitro Data

BACKGROUND: Men are more severely affected by COVID-19. Testosterone may influence SARS-CoV-2 infection and the immune response. OBJECTIVE: To clinically, epidemiologically, and experimentally evaluate the effect of antiandrogens on SARS-CoV-2 infection. DESIGNS, SETTINGS, AND PARTICIPANTS: A random...

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Autores principales: Welén, Karin, Rosendal, Ebba, Gisslén, Magnus, Lenman, Annasara, Freyhult, Eva, Fonseca-Rodríguez, Osvaldo, Bremell, Daniel, Stranne, Johan, Balkhed, Åse Östholm, Niward, Katarina, Repo, Johanna, Robinsson, David, Henningsson, Anna J., Styrke, Johan, Angelin, Martin, Lindquist, Elisabeth, Allard, Annika, Becker, Miriam, Rudolfsson, Stina, Buckland, Robert, Carlsson, Camilla Thellenberg, Bjartell, Anders, Nilsson, Anna C., Ahlm, Clas, Connolly, Anne-Marie Fors, Överby, Anna K., Josefsson, Andreas
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Authors. Published by Elsevier B.V. on behalf of European Association of Urology. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8673828/
https://www.ncbi.nlm.nih.gov/pubmed/34980495
http://dx.doi.org/10.1016/j.eururo.2021.12.013
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author Welén, Karin
Rosendal, Ebba
Gisslén, Magnus
Lenman, Annasara
Freyhult, Eva
Fonseca-Rodríguez, Osvaldo
Bremell, Daniel
Stranne, Johan
Balkhed, Åse Östholm
Niward, Katarina
Repo, Johanna
Robinsson, David
Henningsson, Anna J.
Styrke, Johan
Angelin, Martin
Lindquist, Elisabeth
Allard, Annika
Becker, Miriam
Rudolfsson, Stina
Buckland, Robert
Carlsson, Camilla Thellenberg
Bjartell, Anders
Nilsson, Anna C.
Ahlm, Clas
Connolly, Anne-Marie Fors
Överby, Anna K.
Josefsson, Andreas
author_facet Welén, Karin
Rosendal, Ebba
Gisslén, Magnus
Lenman, Annasara
Freyhult, Eva
Fonseca-Rodríguez, Osvaldo
Bremell, Daniel
Stranne, Johan
Balkhed, Åse Östholm
Niward, Katarina
Repo, Johanna
Robinsson, David
Henningsson, Anna J.
Styrke, Johan
Angelin, Martin
Lindquist, Elisabeth
Allard, Annika
Becker, Miriam
Rudolfsson, Stina
Buckland, Robert
Carlsson, Camilla Thellenberg
Bjartell, Anders
Nilsson, Anna C.
Ahlm, Clas
Connolly, Anne-Marie Fors
Överby, Anna K.
Josefsson, Andreas
author_sort Welén, Karin
collection PubMed
description BACKGROUND: Men are more severely affected by COVID-19. Testosterone may influence SARS-CoV-2 infection and the immune response. OBJECTIVE: To clinically, epidemiologically, and experimentally evaluate the effect of antiandrogens on SARS-CoV-2 infection. DESIGNS, SETTINGS, AND PARTICIPANTS: A randomized phase 2 clinical trial (COVIDENZA) enrolled 42 hospitalized COVID-19 patients before safety evaluation. We also conducted a population-based retrospective study of 7894 SARS-CoV-2–positive prostate cancer patients and an experimental study using an air-liquid interface three-dimensional culture model of primary lung cells. INTERVENTION: In COVIDENZA, patients were randomized 2:1 to 5 d of enzalutamide or standard of care. OUTCOME MEASUREMENTS: The primary outcomes in COVIDENZA were the time to mechanical ventilation or discharge from hospital. The population-based study investigated risk of hospitalization, intensive care, and death from COVID-19 after androgen inhibition. RESULTS AND LIMITATIONS: Enzalutamide-treated patients required longer hospitalization (hazard ratio [HR] for discharge from hospital 0.43, 95% confidence interval [CI] 0.20–0.93) and the trial was terminated early. In the epidemiological study, no preventive effects were observed. The frail population of patients treated with androgen deprivation therapy (ADT) in combination with abiraterone acetate or enzalutamide had a higher risk of dying from COVID-19 (HR 2.51, 95% CI 1.52–4.16). In vitro data showed no effect of enzalutamide on virus replication. The epidemiological study has limitations that include residual confounders. CONCLUSIONS: The results do not support a therapeutic effect of enzalutamide or preventive effects of bicalutamide or ADT in COVID-19. Thus, these antiandrogens should not be used for hospitalized COVID-19 patients or as prevention for COVID-19. Further research on these therapeutics in this setting are not warranted. PATIENT SUMMARY: We studied whether inhibition of testosterone could diminish COVID-19 symptoms. We found no evidence of an effect in a clinical study or in epidemiological or experimental investigations. We conclude that androgen inhibition should not be used for prevention or treatment of COVID-19.
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spelling pubmed-86738282021-12-16 A Phase 2 Trial of the Effect of Antiandrogen Therapy on COVID-19 Outcome: No Evidence of Benefit, Supported by Epidemiology and In Vitro Data Welén, Karin Rosendal, Ebba Gisslén, Magnus Lenman, Annasara Freyhult, Eva Fonseca-Rodríguez, Osvaldo Bremell, Daniel Stranne, Johan Balkhed, Åse Östholm Niward, Katarina Repo, Johanna Robinsson, David Henningsson, Anna J. Styrke, Johan Angelin, Martin Lindquist, Elisabeth Allard, Annika Becker, Miriam Rudolfsson, Stina Buckland, Robert Carlsson, Camilla Thellenberg Bjartell, Anders Nilsson, Anna C. Ahlm, Clas Connolly, Anne-Marie Fors Överby, Anna K. Josefsson, Andreas Eur Urol Prostate Cancer – Editor’s Choice BACKGROUND: Men are more severely affected by COVID-19. Testosterone may influence SARS-CoV-2 infection and the immune response. OBJECTIVE: To clinically, epidemiologically, and experimentally evaluate the effect of antiandrogens on SARS-CoV-2 infection. DESIGNS, SETTINGS, AND PARTICIPANTS: A randomized phase 2 clinical trial (COVIDENZA) enrolled 42 hospitalized COVID-19 patients before safety evaluation. We also conducted a population-based retrospective study of 7894 SARS-CoV-2–positive prostate cancer patients and an experimental study using an air-liquid interface three-dimensional culture model of primary lung cells. INTERVENTION: In COVIDENZA, patients were randomized 2:1 to 5 d of enzalutamide or standard of care. OUTCOME MEASUREMENTS: The primary outcomes in COVIDENZA were the time to mechanical ventilation or discharge from hospital. The population-based study investigated risk of hospitalization, intensive care, and death from COVID-19 after androgen inhibition. RESULTS AND LIMITATIONS: Enzalutamide-treated patients required longer hospitalization (hazard ratio [HR] for discharge from hospital 0.43, 95% confidence interval [CI] 0.20–0.93) and the trial was terminated early. In the epidemiological study, no preventive effects were observed. The frail population of patients treated with androgen deprivation therapy (ADT) in combination with abiraterone acetate or enzalutamide had a higher risk of dying from COVID-19 (HR 2.51, 95% CI 1.52–4.16). In vitro data showed no effect of enzalutamide on virus replication. The epidemiological study has limitations that include residual confounders. CONCLUSIONS: The results do not support a therapeutic effect of enzalutamide or preventive effects of bicalutamide or ADT in COVID-19. Thus, these antiandrogens should not be used for hospitalized COVID-19 patients or as prevention for COVID-19. Further research on these therapeutics in this setting are not warranted. PATIENT SUMMARY: We studied whether inhibition of testosterone could diminish COVID-19 symptoms. We found no evidence of an effect in a clinical study or in epidemiological or experimental investigations. We conclude that androgen inhibition should not be used for prevention or treatment of COVID-19. The Authors. Published by Elsevier B.V. on behalf of European Association of Urology. 2022-03 2021-12-15 /pmc/articles/PMC8673828/ /pubmed/34980495 http://dx.doi.org/10.1016/j.eururo.2021.12.013 Text en © 2021 The Authors Since January 2020 Elsevier has created a COVID-19 resource centre with free information in English and Mandarin on the novel coronavirus COVID-19. The COVID-19 resource centre is hosted on Elsevier Connect, the company's public news and information website. Elsevier hereby grants permission to make all its COVID-19-related research that is available on the COVID-19 resource centre - including this research content - immediately available in PubMed Central and other publicly funded repositories, such as the WHO COVID database with rights for unrestricted research re-use and analyses in any form or by any means with acknowledgement of the original source. These permissions are granted for free by Elsevier for as long as the COVID-19 resource centre remains active.
spellingShingle Prostate Cancer – Editor’s Choice
Welén, Karin
Rosendal, Ebba
Gisslén, Magnus
Lenman, Annasara
Freyhult, Eva
Fonseca-Rodríguez, Osvaldo
Bremell, Daniel
Stranne, Johan
Balkhed, Åse Östholm
Niward, Katarina
Repo, Johanna
Robinsson, David
Henningsson, Anna J.
Styrke, Johan
Angelin, Martin
Lindquist, Elisabeth
Allard, Annika
Becker, Miriam
Rudolfsson, Stina
Buckland, Robert
Carlsson, Camilla Thellenberg
Bjartell, Anders
Nilsson, Anna C.
Ahlm, Clas
Connolly, Anne-Marie Fors
Överby, Anna K.
Josefsson, Andreas
A Phase 2 Trial of the Effect of Antiandrogen Therapy on COVID-19 Outcome: No Evidence of Benefit, Supported by Epidemiology and In Vitro Data
title A Phase 2 Trial of the Effect of Antiandrogen Therapy on COVID-19 Outcome: No Evidence of Benefit, Supported by Epidemiology and In Vitro Data
title_full A Phase 2 Trial of the Effect of Antiandrogen Therapy on COVID-19 Outcome: No Evidence of Benefit, Supported by Epidemiology and In Vitro Data
title_fullStr A Phase 2 Trial of the Effect of Antiandrogen Therapy on COVID-19 Outcome: No Evidence of Benefit, Supported by Epidemiology and In Vitro Data
title_full_unstemmed A Phase 2 Trial of the Effect of Antiandrogen Therapy on COVID-19 Outcome: No Evidence of Benefit, Supported by Epidemiology and In Vitro Data
title_short A Phase 2 Trial of the Effect of Antiandrogen Therapy on COVID-19 Outcome: No Evidence of Benefit, Supported by Epidemiology and In Vitro Data
title_sort phase 2 trial of the effect of antiandrogen therapy on covid-19 outcome: no evidence of benefit, supported by epidemiology and in vitro data
topic Prostate Cancer – Editor’s Choice
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8673828/
https://www.ncbi.nlm.nih.gov/pubmed/34980495
http://dx.doi.org/10.1016/j.eururo.2021.12.013
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