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Androgen-deprivation therapies for prostate cancer and risk of infection by SARS-CoV-2: a population-based study (N = 4532).
Montopoli, M; Zumerle, S; Vettor, R; Rugge, M; Zorzi, M; Catapano, C V; Carbone, G M; Cavalli, A; Pagano, F; Ragazzi, E; Prayer-Galetti, T; Alimonti, A.
  • Montopoli M; Department of Pharmaceutical and Pharmacological Sciences, Università degli Studi di Padova, Padova, Italy; VIMM - Veneto Institute of Molecular Medicine, Fondazione per la Ricerca Biomedica Avanzata, Padova, Italy.
  • Zumerle S; VIMM - Veneto Institute of Molecular Medicine, Fondazione per la Ricerca Biomedica Avanzata, Padova, Italy; Department of Medicine, Università degli Studi di Padova, Padova, Italy.
  • Vettor R; Department of Medicine, Università degli Studi di Padova, Padova, Italy.
  • Rugge M; Department of Medicine, Università degli Studi di Padova, Padova, Italy; Veneto Tumour Registry - Azienda Zero, Padova, Italy.
  • Zorzi M; Veneto Tumour Registry - Azienda Zero, Padova, Italy.
  • Catapano CV; Institute of Oncology Research, Oncology Institute of Southern Switzerland, Università della Svizzera Italiana, Bellinzona, Switzerland.
  • Carbone GM; Institute of Oncology Research, Oncology Institute of Southern Switzerland, Università della Svizzera Italiana, Bellinzona, Switzerland.
  • Cavalli A; Institute for Research in Biomedicine, Università della Svizzera Italiana, Bellinzona, Switzerland.
  • Pagano F; VIMM - Veneto Institute of Molecular Medicine, Fondazione per la Ricerca Biomedica Avanzata, Padova, Italy.
  • Ragazzi E; Department of Pharmaceutical and Pharmacological Sciences, Università degli Studi di Padova, Padova, Italy.
  • Prayer-Galetti T; Department of Oncological and Gastroenterological Sciences - Urology Unit, Azienda Ospedaliera di Padova, Padova, Italy.
  • Alimonti A; VIMM - Veneto Institute of Molecular Medicine, Fondazione per la Ricerca Biomedica Avanzata, Padova, Italy; Department of Medicine, Università degli Studi di Padova, Padova, Italy; Institute of Oncology Research, Oncology Institute of Southern Switzerland, Università della Svizzera Italiana, Bellinz
Ann Oncol ; 31(8): 1040-1045, 2020 08.
Article in English | MEDLINE | ID: covidwho-186722
ABSTRACT

BACKGROUND:

Cell entry of severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) depends on binding of the viral spike (S) proteins to angiotensin-converting enzyme 2 and on S protein priming by TMPRSS2. Inhibition of TMPRSS2 may work to block or decrease the severity of SARS-CoV-2 infections. Intriguingly, TMPRSS2 is an androgen-regulated gene that is up-regulated in prostate cancer where it supports tumor progression and is involved in a frequent genetic translocation with the ERG gene. First- or second-generation androgen-deprivation therapies (ADTs) decrease the levels of TMPRSS2. Here we put forward the hypothesis that ADTs may protect patients affected by prostate cancer from SARS-CoV-2 infections. MATERIALS AND

METHODS:

We extracted data regarding 9280 patients (4532 males) with laboratory-confirmed SARS-CoV-2 infection from 68 hospitals in Veneto, one of the Italian regions that was most affected by the coronavirus disease 2019 (COVID-19) pandemic. The parameters used for each COVID-19-positive patient were sex, hospitalization, admission to intensive care unit, death, tumor diagnosis, prostate cancer diagnosis, and ADT.

RESULTS:

There were evaluable 9280 SARS-CoV-2-positive patients in Veneto on 1 April 2020. Overall, males developed more severe complications, were more frequently hospitalized, and had a worse clinical outcome than females. Considering only the Veneto male population (2.4 million men), 0.2% and 0.3% of non-cancer and cancer patients, respectively, tested positive for SARS-CoV-2. Comparing the total number of SARS-CoV-2-positive cases, prostate cancer patients receiving ADT had a significantly lower risk of SARS-CoV-2 infection compared with patients who did not receive ADT (OR 4.05; 95% CI 1.55-10.59). A greater difference was found comparing prostate cancer patients receiving ADT with patients with any other type of cancer (OR 4.86; 95% CI 1.88-12.56).

CONCLUSION:

Our data suggest that cancer patients have an increased risk of SARS-CoV-2 infections compared with non-cancer patients. However, prostate cancer patients receiving ADT appear to be partially protected from SARS-CoV-2 infections.
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Full text: Available Collection: International databases Database: MEDLINE Main subject: Pneumonia, Viral / Prostatic Neoplasms / Population Surveillance / Coronavirus Infections / Pandemics / Betacoronavirus / Androgen Antagonists Type of study: Diagnostic study / Observational study / Prognostic study Limits: Aged / Humans / Male / Middle aged Country/Region as subject: Europa Language: English Journal: Ann Oncol Journal subject: Neoplasms Year: 2020 Document Type: Article Affiliation country: J.annonc.2020.04.479

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Full text: Available Collection: International databases Database: MEDLINE Main subject: Pneumonia, Viral / Prostatic Neoplasms / Population Surveillance / Coronavirus Infections / Pandemics / Betacoronavirus / Androgen Antagonists Type of study: Diagnostic study / Observational study / Prognostic study Limits: Aged / Humans / Male / Middle aged Country/Region as subject: Europa Language: English Journal: Ann Oncol Journal subject: Neoplasms Year: 2020 Document Type: Article Affiliation country: J.annonc.2020.04.479