Literature DB >> 33007381

Androgen deprivation therapy in unlikely to be effective for treatment of COVID-19.

M E O'Callaghan1, A Jay2, G Kichenadasse3, K L Moretti4.   

Abstract

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Year:  2020        PMID: 33007381      PMCID: PMC7525325          DOI: 10.1016/j.annonc.2020.09.014

Source DB:  PubMed          Journal:  Ann Oncol        ISSN: 0923-7534            Impact factor:   32.976


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Recent literature has reported that patients with prostate cancer treated with androgen deprivation therapy (ADT) have a lower incidence of severe acute respiratory syndrome coronavirus 2 (SARS-COV-2), an observation which has been widely reported by media outlets, together with speculation that ADT may be a potential treatment for coronavirus disease 2019 (COVID-19). The study by Montopoli et al. was conducted at a population level in Italy, a region experiencing a high level of COVID-19 cases. They observed in a cohort of men with prostate cancer that those prescribed ADT were less likely to report COVID-19 (4/5273 cases versus 114/37 161, odds ratio 4.05, 95% confidence interval 1.55–10.59, P = 0.00043). Benefits were also observed for classification of mild and severe disease and were used as a basis of the conclusion that ‘ADT, based on luteinizing hormone-releasing hormone (LHRH) agonist/antagonists or AR inhibitors, may be considered to reduce SARS-CoV-2 infections or complications in high-risk male populations.’ A useful metric to consider in this context is the number needed to treat, which is calculable from the data reported, but was not included by Montopoli et al. We calculate that the number needed to treat with ADT for the prevention of one COVID-19 case is 434. Treatment of these cases is not without risk and this is shown in Figure 1 with data extracted from Bagrodia et al. In addition, diabetes mellitus, decreased libido, hot flashes and erectile dysfunction would be expected in a high proportion of men. These adverse events are calculated per person-year, a time frame which may be relevant to prevention of COVID-19. Montopoli et al. state that ADT could be administered transiently to minimise adverse events, though this hypothesis has not been tested in the data they present. Transient ADT treatment may be appropriate to reduce complications in those already infected with SARS-COV-2, although ADT adverse events are typically most common immediately after commencement.
Figure 1

ADT treatment for COVID 19 in context.

ADT, androgen deprivation therapy; COVID-19, coronavirus disease 2019.

ADT treatment for COVID 19 in context. ADT, androgen deprivation therapy; COVID-19, coronavirus disease 2019. The mechanism of action which Montopoli et al. describe may provide a novel target for COVID-19 treatments, but it seems unlikely that existing ADTs will provide a viable treatment option.
  3 in total

1.  Risk and timing of cardiovascular disease after androgen-deprivation therapy in men with prostate cancer.

Authors:  Sean O'Farrell; Hans Garmo; Lars Holmberg; Jan Adolfsson; Pär Stattin; Mieke Van Hemelrijck
Journal:  J Clin Oncol       Date:  2015-03-02       Impact factor: 44.544

2.  Androgen-deprivation therapies for prostate cancer and risk of infection by SARS-CoV-2: a population-based study (N = 4532).

Authors:  M Montopoli; S Zumerle; R Vettor; M Rugge; M Zorzi; C V Catapano; G M Carbone; A Cavalli; F Pagano; E Ragazzi; T Prayer-Galetti; A Alimonti
Journal:  Ann Oncol       Date:  2020-05-06       Impact factor: 32.976

3.  Adverse effects of androgen deprivation therapy in prostate cancer: Current management issues.

Authors:  Aditya Bagrodia; Christopher J Diblasio; Robert W Wake; Ithaar H Derweesh
Journal:  Indian J Urol       Date:  2009-04
  3 in total
  3 in total

Review 1.  Impact of the SARS-CoV-2 virus on male reproductive health.

Authors:  Daniel E Nassau; Jordan C Best; Eliyahu Kresch; Daniel C Gonzalez; Kajal Khodamoradi; Ranjith Ramasamy
Journal:  BJU Int       Date:  2021-08-31       Impact factor: 5.969

2.  Association between SARS-CoV-2 infection and disease severity among prostate cancer patients on androgen deprivation therapy: a systematic review and meta-analysis.

Authors:  Reza Sari Motlagh; Mohammad Abufaraj; Pierre I Karakiewicz; Pawel Rajwa; Keiichiro Mori; Dong-Ho Mun; Shahrokh F Shariat
Journal:  World J Urol       Date:  2021-09-03       Impact factor: 3.661

3.  Topical TMPRSS2 inhibition prevents SARS-CoV-2 infection in differentiated human airway cultures.

Authors:  Wenrui Guo; Linsey M Porter; Thomas Wm Crozier; Matthew Coates; Akhilesh Jha; Mikel McKie; James A Nathan; Paul J Lehner; Edward Jd Greenwood; Frank McCaughan
Journal:  Life Sci Alliance       Date:  2022-02-02
  3 in total

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