Cancers (May 2023)

Evaluation of Semen Self-Sampling Yield Predictors and CTC Isolation by Multi-Color Flow Cytometry for Liquid Biopsy of Localized Prostate Cancer

  • Cesare Saitta,
  • Ilaria De Simone,
  • Vittorio Fasulo,
  • Marinella Corbetta,
  • Stefano Duga,
  • Chiara Chiereghin,
  • Federico Simone Colombo,
  • Alessio Benetti,
  • Roberto Contieri,
  • Pier Paolo Avolio,
  • Alessandro Uleri,
  • Alberto Saita,
  • Giorgio Ferruccio Guazzoni,
  • Rodolfo Hurle,
  • Piergiuseppe Colombo,
  • Nicolò Maria Buffi,
  • Paolo Casale,
  • Giovanni Lughezzani,
  • Rosanna Asselta,
  • Giulia Soldà,
  • Massimo Lazzeri

DOI
https://doi.org/10.3390/cancers15102666
Journal volume & issue
Vol. 15, no. 10
p. 2666

Abstract

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Liquid biopsy (LB) for prostate cancer (PCa) detection could represent an alternative to biopsy. Seminal fluid (SF) is a source of PCa-specific biomarkers, as 40% of ejaculate derives from the prostate. We tested the feasibility of an SF-based LB by evaluating the yield of semen self-sampling in a cohort of >750 patients with clinically localized PCa. The overall SF collection yield was 18.2% (39% when considering only compliant patients), with about a half of the patients (53.15%) not consenting to SF donation. Independent favorable predictors for SF collection were younger age and lower prostate volume. We implemented a protocol to enrich prostate-derived cells by multi-color flow cytometry and applied it on SF and urine samples from 100 patients. The number of prostate-enriched cells (SYTO-16+ PSMA+ CD45−) was variable, with higher numbers of cells isolated from SF than urine (p value high) were 2% of isolated cells in both specimens. The fraction of EpCAMhigh cells over prostate-enriched cells (PSMA+) significantly correlated with patient age in both semen and urine, but not with other clinical parameters, such as Gleason Score, ISUP, or TNM stage. Hence, enumeration of prostate-derived cells is not sufficient to guide PCa diagnosis; additional molecular analyses to detect patient-specific cancer lesions will be needed.

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