Prostate Cancer in Renal Transplant Recipients: Results from a Large Contemporary Cohort

  • Giancarlo Marra
  • Francesco Soria
  • Federica Peretti
  • Marco Oderda
  • Charles Dariane
  • Marc-Olivier Timsit
  • Julien Branchereau
  • Oussama Hedli
  • Benoit Mesnard
  • Derya Tilki
  • Jonathon Olsburgh
  • Meghana Kulkarni
  • Veeru Kasivisvanathan
  • Cedric Lebacle
  • Oscar Rodriguez-Faba
  • Alberto Breda
  • Timo Soeterik
  • Giorgio Gandaglia
  • Paola Todeschini
  • Luigi Biancone
  • Paolo Gontero
  • On Behalf Of The Collaborators

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Abstract

Objectives: The aim of this study was to assess the natural history of prostate cancer (PCa) in renal transplant recipients (RTRs) and to clarify the controversy over whether RTRs have a higher risk of PCa and poorer outcomes than non-RTRs, due to factors such as immunosuppression. Patients and Methods: We performed a retrospective multicenter study of RTRs diagnosed with cM0 PCa between 2001 and 2019. Primary outcomes were overall (OS) and cancer-specific survival (CSS). Secondary outcomes included biochemical recurrence and/or progression after active surveillance (AS) and evaluation of variables possibly influencing PCa aggressiveness and outcomes. Management modalities included surgery, radiation, cryotherapy, HIFU, AS, and watchful waiting. Results: We included 166 men from nine institutions. Median age and eGFR at diagnosis were 67 (IQR 60−73) and 45.9 mL/min (IQR 31.5−63.4). ASA score was >2 in 58.4% of cases. Median time from transplant to PCa diagnosis was 117 months (IQR 48−191.5), and median PSA at diagnosis was 6.5 ng/mL (IQR 5.02−10). The biopsy Gleason score was ≥8 in 12.8%; 11.6% and 6.1% patients had suspicion of ≥cT3 > cT2 and cN+ disease. The most frequent management method was radical prostatectomy (65.6%), followed by radiation therapy (16.9%) and AS (10.2%). At a median follow-up of 60.5 months (IQR 31−106) 22.9% of men (n = 38) died, with only n = 4 (2.4%) deaths due to PCa. Local and systemic progression rates were 4.2% and 3.0%. On univariable analysis, no major influence of immunosuppression type was noted, with the exception of a protective effect of antiproliferative agents (HR 0.39, 95% CI 0.16−0.97, p = 0.04) associated with a decreased risk of biochemical recurrence (BCR) or progression after AS. Conclusion: PCa diagnosed in RTRs is mainly of low to intermediate risk and organ-confined at diagnosis, with good cancer control and low PCa death at intermediate follow-up. RTRs have a non-negligible risk of death from causes other than PCa. Aggressive upfront management of the majority of RTRs with PCa may, therefore, be avoided.

Bibliographical data

Original languageEnglish
Article number189
ISSN2072-6694
DOIs
Publication statusPublished - 28.12.2022
PubMed 36612184