Androgen deprivation therapy, comorbidity, cancer stage and mortality from COVID-19 in men with prostate cancer.


Journal

Scandinavian journal of urology
ISSN: 2168-1813
Titre abrégé: Scand J Urol
Pays: Sweden
ID NLM: 101587186

Informations de publication

Date de publication:
Apr 2022
Historique:
pubmed: 24 12 2021
medline: 30 4 2022
entrez: 23 12 2021
Statut: ppublish

Résumé

Androgens facilitate entrance of the severe acute respiratory syndrome coronavirus 2 into respiratory epithelial cells, and male sex is associated with a higher risk of death from corona virus disease (COVID-19). Androgen deprivation therapy (ADT) could possibly improve COVID-19 outcomes. In a case-control study nested in the Prostate Cancer data Base Sweden (PCBaSe) RAPID 2019, we evaluated the association between ADT and COVID-19 as registered cause of death in men with prostate cancer. Each case was matched to 50 controls by region. We used conditional logistic regression to adjust for confounders and also evaluated potential impact of residual confounding. We identified 474 men who died from COVID-19 in March-December 2020. In crude analyses, ADT exposure was associated with an increased risk of COVID-19 death (odds ratio [OR] 5.05, 95% CI: 4.18-6.10); however, the OR was substantially attenuated after adjustment for age, comorbidity, prostate cancer characteristics at diagnosis, recent healthcare use, and indicators of advanced cancer (adjusted OR 1.25, 95% CI: 0.95-1.65). If adjustment has accounted for at least 85% of confounding, then the true effect could be no more than a 5% reduction of the odds for COVID-19 death. The increased mortality from COVID-19 in men with prostate cancer treated with ADT was mainly related to high age, comorbidity, and more advanced prostate cancer. There was no evidence to support the hypothesis that ADT is associated with improved COVID-19 outcomes.

Sections du résumé

BACKGROUND BACKGROUND
Androgens facilitate entrance of the severe acute respiratory syndrome coronavirus 2 into respiratory epithelial cells, and male sex is associated with a higher risk of death from corona virus disease (COVID-19). Androgen deprivation therapy (ADT) could possibly improve COVID-19 outcomes.
METHODS METHODS
In a case-control study nested in the Prostate Cancer data Base Sweden (PCBaSe) RAPID 2019, we evaluated the association between ADT and COVID-19 as registered cause of death in men with prostate cancer. Each case was matched to 50 controls by region. We used conditional logistic regression to adjust for confounders and also evaluated potential impact of residual confounding.
RESULTS RESULTS
We identified 474 men who died from COVID-19 in March-December 2020. In crude analyses, ADT exposure was associated with an increased risk of COVID-19 death (odds ratio [OR] 5.05, 95% CI: 4.18-6.10); however, the OR was substantially attenuated after adjustment for age, comorbidity, prostate cancer characteristics at diagnosis, recent healthcare use, and indicators of advanced cancer (adjusted OR 1.25, 95% CI: 0.95-1.65). If adjustment has accounted for at least 85% of confounding, then the true effect could be no more than a 5% reduction of the odds for COVID-19 death.
CONCLUSIONS CONCLUSIONS
The increased mortality from COVID-19 in men with prostate cancer treated with ADT was mainly related to high age, comorbidity, and more advanced prostate cancer. There was no evidence to support the hypothesis that ADT is associated with improved COVID-19 outcomes.

Identifiants

pubmed: 34939533
doi: 10.1080/21681805.2021.2019304
doi:

Substances chimiques

Androgen Antagonists 0
Androgens 0

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

104-111

Auteurs

Rolf Gedeborg (R)

Department of Surgical Sciences, Uppsala University, Uppsala, Sweden.

Lars Lindhagen (L)

Uppsala Clinical Research Center (UCR), Uppsala, Sweden.

Stacy Loeb (S)

Department of Urology and Population Health, New York University and Manhattan Veterans Affairs Medical Center, New York, NY, USA.

Johan Styrke (J)

Department of Surgical and Perioperative Sciences, Urology and Andrology, Umeå University, Umeå, Sweden.

Hans Garmo (H)

Department of Surgical Sciences, Uppsala University, Uppsala, Sweden.
Translational Oncology and Urology Research (TOUR), King's College London, Guy's Hospital, London, UK.

Pär Stattin (P)

Department of Surgical Sciences, Uppsala University, Uppsala, Sweden.

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Classifications MeSH