TY - JOUR
T1 - Mass Spectrometry-Based Biomarkers to Detect Prostate Cancer
T2 - A Multicentric Study Based on Non-Invasive Urine Collection without Prior Digital Rectal Examination
AU - Frantzi, Maria
AU - Culig, Zoran
AU - Heidegger, Isabel
AU - Mokou, Marika
AU - Latosinska, Agnieszka
AU - Roesch, Marie C.
AU - Merseburger, Axel S.
AU - Makridakis, Manousos
AU - Vlahou, Antonia
AU - Blanca-Pedregosa, Ana
AU - Carrasco-Valiente, Julia
AU - Mischak, Harald
AU - Gomez-Gomez, Enrique
N1 - Publisher Copyright:
© 2023 by the authors.
PY - 2023/2/11
Y1 - 2023/2/11
N2 - (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.
AB - (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.
UR - http://www.scopus.com/inward/record.url?scp=85149200347&partnerID=8YFLogxK
UR - https://www.mendeley.com/catalogue/5dddf81e-2dec-35ef-8e8e-345b30826b11/
U2 - 10.3390/cancers15041166
DO - 10.3390/cancers15041166
M3 - Journal articles
C2 - 36831508
AN - SCOPUS:85149200347
SN - 2072-6694
VL - 15
JO - Cancers
JF - Cancers
IS - 4
M1 - 1166
ER -