Evidence map›Paper›PMID 34517429›Full record

ArticleThe Prostate2021

Influence of androgen deprivation therapy on the severity of COVID-19 in prostate cancer patients.

Estíbaliz Jiménez-Alcaide, Clara García-Fuentes, Virginia Hernández, Enrique De la Peña, Elia Pérez-Fernández, Alejandro Castro, Begoña Caballero-Perea, Ana Guijarro, Carlos Llorente

Open access · bronzeAbstract read
In one paragraph

Article in The Prostate, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers, 3 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed, 3 pooled it
1.4field-weighted citation impact, top 15% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

11 citing papers in PubMed, 3 syntheses or guidelines pooled it, 16 citations in OpenAlex.

  1. [Prostate cancer, androgen deprivation, and risk of COVID-19 infection : A systematic review and meta-analysis].Progres en urologie : journal de l'Association francaise d'urologie et de la Societe francaise d'urologie · 2022
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  9. Examining Male Predominance of Severe COVID-19 Outcomes: A Systematic Review.Androgens: clinical research and therapeutics · 2022
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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

9 authors at 2 institutions in 1 country.

Estíbaliz Jiménez-AlcaideDepartment of Urology, Hospital Universitario Fundación Alcorcón, Madrid, Spain.ORCID 0000-0002-0941-1485
Clara García-FuentesDepartment of Urology, Hospital Universitario Fundación Alcorcón, Madrid, Spain.
Virginia HernándezDepartment of Urology, Hospital Universitario Fundación Alcorcón, Madrid, Spain.
Enrique De la PeñaDepartment of Urology, Hospital Universitario Fundación Alcorcón, Madrid, Spain.
Elia Pérez-FernándezResearch Unit, Hospital Universitario Fundación Alcorcón, Madrid, Spain.
Alejandro CastroDepartment of Urology, Hospital Universitario Fundación Alcorcón, Madrid, Spain.
Begoña Caballero-PereaDepartment of Radiation Oncology, Hospital Universitario de Fuenlabrada, Madrid, Spain.
Ana GuijarroDepartment of Urology, Hospital Universitario Fundación Alcorcón, Madrid, Spain.
Carlos LlorenteDepartment of Urology, Hospital Universitario Fundación Alcorcón, Madrid, Spain.
Hospital Universitario Fundación Alcorcón · ESHospital Universitario de Fuenlabrada · ES

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundThe TMPRSS2 protein has been involved in severe acute respiratory syndrome caused by coronavirus 2 (SARS-CoV-2). The production is regulated by the androgen receptor (AR). It is speculated that androgen deprivation therapy (ADT) may protect patients affected by prostate cancer (PC) from SARS-CoV-2 infection.

methodsThis is a retrospective study of patients treated for COVID-19 in our institution who had a previous diagnosis of PC. We analyzed the influence of exposure of ADT on the presence of severe course of COVID-19.

resultsA total of 2280 patients were treated in our center for COVID-19 with a worse course of disease in males (higher rates of hospitalization, intense care unit [ICU] admission, and death). Out of 1349 subjects registered in our PC database, 156 were on ADT and 1193 were not. Out of those, 61 (4.52%) PC patients suffered from COVID-19, 11 (18.0%) belonged to the ADT group, and 50 (82.0%) to the non-ADT group. Regarding the influence of ADT on the course of the disease, statistically significant differences were found neither in the death rate (27.3% vs. 34%; p = 0.481), nor in the presence of severe COVID-19: need for intubation or ICU admission (0% vs. 6.3%; p = 0.561) and need for corticoid treatment, interferon beta, or tocilizumab (60% vs. 34.7%; p = 0.128). Multivariate analysis adjusted for clinically relevant comorbidities did not find that ADT was a protective factor for worse clinical evolution (risk ratio [RR] 1.08; 95% confidence interval [CI], 0.64-1.83; p = 0.77) or death (RR, 0.67; 95% CI, 0.26-1.74; p = 0.41).

conclusionsOur study confirms that COVID-19 is more severe in men. However, the use of ADT in patients with PC was not shown to prevent the risk of severe COVID-19.

Indexed as

SARS-CoV-2Severity of Illness IndexAgedAged, 80 and overAndrogen AntagonistsComorbidityCOVID-19HospitalizationHumansIntensive Care UnitsMaleMiddle AgedNeoplasm StagingProstatic NeoplasmsRetrospective StudiesRisk FactorsAndrogen Antagonistsandrogen deprivation therapyCOVID-19prostatic neoplasmsSARS-CoV-2

Identifiers

PMID34517429
PMCPMC8661752
OpenAlexW3199127189

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.