CASE REPORT article
Front. Oncol.
Sec. Genitourinary Oncology
Volume 15 - 2025 | doi: 10.3389/fonc.2025.1679663
This article is part of the Research TopicHistological and Molecular Subtypes of Prostate Cancer: Biology, Biomarkers, and Therapeutic ImplicationsView all 3 articles
Prostate Cancer Evolution After COVID-19-Related Prostatitis in a TMPRSS2-Altered Patient A Case Report and Review of the Molecular Interface Between SARS-CoV-2 and Prostate Oncogenesis
Provisionally accepted- State University of Rio de Janeiro, Rio de Janeiro, Brazil
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Background: SARS-CoV-2 exploits TMPRSS2, an androgen-regulated protease highly expressed in prostate tissue, to enter host cells. While inflammation is a recognized promoter of oncogenesis, the possibility that viral prostatitis could precede prostate cancer has not been previously reported. Case Presentation: We describe the case of a 55-year-old male with no family history of prostate or breast cancer and no germline pathogenic variants on next-generation sequencing (NGS), who developed lower urinary tract symptoms (LUTS) and PSA elevation shortly after a second COVID-19 infection. Multiparametric MRI initially demonstrated diffuse PI-RADS 4 changes compatible with prostatitis (Figure 1). Although symptoms improved with antibiotics, LUTS persisted and were managed with finasteride and doxazosin. Over the following two years, serial imaging revealed progression to a long, poorly demarcated PI-RADS 5 lesion extending from apex to base in the right posterior peripheral zone, and a smaller PI-RADS 4 lesion on the left (Figure 2). Targeted biopsy confirmed acinar adenocarcinoma (Gleason 7 and 6 in 16 of 26 cores). PET-PSMA showed disease confined to the prostate. The patient underwent neoadjuvant therapy with androgen deprivation therapy (ADT) plus a novel hormonal agent (NHA) from April 14 to October 15, 2024, resulting in significant tumor reduction. Radical prostatectomy on November 1, 2024 revealed a small residual acinar adenocarcinoma focus with perineural invasion, negative surgical margins, and molecular evidence of TMPRSS2::ERG gene fusion and PTEN loss (Figure 3). Conclusion: This is the first documented case suggesting a potential link between COVID-19-related prostatitis and subsequent prostate cancer in a TMPRSS2::ERG-altered patient without hereditary predisposition. Although causality cannot be established, the findings highlight a hypothesis-generating interface between viral infection, inflammation, and oncogenesis that warrants further study.
Keywords: SARS-CoV-2, tmprss2, COVID-19, Prostatitis, prostate cancer, ERG fusion, Pten, novel hormonal agent
Received: 04 Aug 2025; Accepted: 20 Oct 2025.
Copyright: © 2025 Carrerette, Gomes, de Oliveira, Santiago, Coelho, Rodeiro, Polonia, Guedes and Oliveira. This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) or licensor are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
* Correspondence: Fabricio Borges Carrerette, carrerette2@gmail.com
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