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

Author:

Saitta Cesare12,De Simone Ilaria2,Fasulo Vittorio12,Corbetta Marinella2,Duga Stefano23,Chiereghin Chiara2,Colombo Federico Simone3,Benetti Alessio1,Contieri Roberto12ORCID,Avolio Pier Paolo12,Uleri Alessandro12,Saita Alberto1,Guazzoni Giorgio Ferruccio12,Hurle Rodolfo1,Colombo Piergiuseppe24,Buffi Nicolò Maria12,Casale Paolo1,Lughezzani Giovanni12,Asselta Rosanna23ORCID,Soldà Giulia23ORCID,Lazzeri Massimo1

Affiliation:

1. Department of Urology, IRCCS Humanitas Research Hospital, 20089 Rozzano, Italy

2. Department of Biomedical Sciences, Humanitas University, 20072 Pieve Emanuele, Italy

3. Flow Cytometry Core, IRCCS Humanitas Research Hospital, 20089 Rozzano, Italy

4. Department of Pathology, IRCCS Humanitas Research Hospital, 20089 Rozzano, Italy

Abstract

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 < 0.001). Putative cancer cells (EpCAMhigh) 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.

Funder

Italian Ministry of Health

Publisher

MDPI AG

Subject

Cancer Research,Oncology

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