Mass Spectrometry-Based Biomarkers to Detect Prostate Cancer: A Multicentric Study Based on Non-Invasive Urine Collection without Prior Digital Rectal Examination

Author:

Frantzi Maria1ORCID,Culig Zoran2,Heidegger Isabel2ORCID,Mokou Marika1ORCID,Latosinska Agnieszka1,Roesch Marie C.3,Merseburger Axel S.3,Makridakis Manousos4ORCID,Vlahou Antonia4ORCID,Blanca-Pedregosa Ana5ORCID,Carrasco-Valiente Julia5,Mischak Harald16,Gomez-Gomez Enrique5

Affiliation:

1. Department of Biomarker Research, Mosaiques Diagnostics GmbH, 30659 Hannover, Germany

2. Experimental Urology Department of Urology, Medical University of Innsbruck, 6020 Innsbruck, Austria

3. Department of Urology, University Hospital Schleswig-Holstein, Campus Lübeck, 23538 Lübeck, Germany

4. Systems Biology Center, Biomedical Research Foundation, Academy of Athens, 11527 Athens, Greece

5. Maimonides Biomedical Research Institute of Córdoba, Department of Urology, University of Cordoba, 14004 Cordoba, Spain

6. Institute of Cardiovascular and Medical Science, University of Glasgow, Glasgow G12 8TA, UK

Abstract

(1) Background: Prostate cancer (PCa) is the most frequently diagnosed cancer in men. Wide application of prostate specific antigen test has historically led to over-treatment, starting from excessive biopsies. Risk calculators based on molecular and clinical variables can be of value to determine the risk of PCa and as such, reduce unnecessary and invasive biopsies. Urinary molecular studies have been mostly focusing on sampling after initial intervention (digital rectal examination and/or prostate massage). (2) Methods: Building on previous proteomics studies, in this manuscript, we aimed at developing a biomarker model for PCa detection based on urine sampling without prior intervention. Capillary electrophoresis coupled to mass spectrometry was applied to acquire proteomics profiles from 970 patients from two different clinical centers. (3) Results: A case-control comparison was performed in a training set of 413 patients and 181 significant peptides were subsequently combined by a support vector machine algorithm. Independent validation was initially performed in 272 negative for PCa and 138 biopsy-confirmed PCa, resulting in an AUC of 0.81, outperforming current standards, while a second validation phase included 147 PCa patients. (4) Conclusions: This multi-dimensional biomarker model holds promise to improve the current diagnosis of PCa, by guiding invasive biopsies.

Funder

BioGuidePCa

European Social Funds

Spanish grant ICSIII

BMBF

Publisher

MDPI AG

Subject

Cancer Research,Oncology

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