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Urinary Marker Panels for Aggressive Prostate Cancer Detection

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Journal Sci Rep
Specialty Science
Date 2022 Sep 1
PMID 36050450
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Abstract

Majority of patients with indolent prostate cancer (PCa) can be managed with active surveillance. Therefore, finding biomarkers for classifying patients between indolent and aggressive PCa is essential. In this study, we investigated urinary marker panels composed of urinary glycopeptides and/or urinary prostate-specific antigen (PSA) for their clinical utility in distinguishing non-aggressive (Grade Group 1) from aggressive (Grade Group ≥ 2) PCa. Urinary glycopeptides acquired via data-independent acquisition mass spectrometry (DIA-MS) were quantitatively analyzed, where prostatic acid phosphatase (ACPP), clusterin (CLU), alpha-1-acid glycoprotein 1 (ORM1), and CD antigen 97 (CD97) were selected to be evaluated in various combinations with and without urinary PSA. Targeted parallel reaction monitoring (PRM) assays of the glycopeptides from urinary ACPP and CLU were investigated along with urinary PSA for the ability of aggressive PCa detection. The multi-urinary marker panels, combined via logistic regression, were statistically evaluated using bootstrap resampling and validated by an independent cohort. Majority of the multi-urinary marker panels (e.g., a panel consisted of ACPP, CLU, and Urinary PSA) achieved area under the curve (AUC) ranged from 0.70 to 0.85. Thus, multi-marker panels investigated in this study showed clinically meaningful results on aggressive PCa detection to separate Grade Group 1 from Grade Group 2 and above warranting further evaluation in clinical setting in future.

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References
1.
Kinsella N, Stattin P, Cahill D, Brown C, Bill-Axelson A, Bratt O . Factors Influencing Men's Choice of and Adherence to Active Surveillance for Low-risk Prostate Cancer: A Mixed-method Systematic Review. Eur Urol. 2018; 74(3):261-280. PMC: 6198662. DOI: 10.1016/j.eururo.2018.02.026. View

2.
Berman D, Epstein J . When is prostate cancer really cancer?. Urol Clin North Am. 2014; 41(2):339-46. DOI: 10.1016/j.ucl.2014.01.006. View

3.
Rodriguez M, Bajo-Santos C, Hessvik N, Lorenz S, Fromm B, Berge V . Identification of non-invasive miRNAs biomarkers for prostate cancer by deep sequencing analysis of urinary exosomes. Mol Cancer. 2017; 16(1):156. PMC: 5629793. DOI: 10.1186/s12943-017-0726-4. View

4.
Hendriks R, van Oort I, Schalken J . Blood-based and urinary prostate cancer biomarkers: a review and comparison of novel biomarkers for detection and treatment decisions. Prostate Cancer Prostatic Dis. 2016; 20(1):12-19. DOI: 10.1038/pcan.2016.59. View

5.
Choo R, Klotz L, Danjoux C, Morton G, Deboer G, Szumacher E . Feasibility study: watchful waiting for localized low to intermediate grade prostate carcinoma with selective delayed intervention based on prostate specific antigen, histological and/or clinical progression. J Urol. 2002; 167(4):1664-9. View