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PCA3 in prostate cancer and tumor aggressiveness detection on 407 high-risk patients: a National Cancer Institute experience

BACKGROUND: Prostate cancer (PCa) is the most common male cancer in Europe and the US. The early diagnosis relies on prostate specific antigen (PSA) serum test, even if it showed clear limits. Among the new tests currently under study, one of the most promising is the prostate cancer gene 3 (PCA3),...

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Autores principales: Merola, Roberta, Tomao, Luigi, Antenucci, Anna, Sperduti, Isabella, Sentinelli, Steno, Masi, Serena, Mandoj, Chiara, Orlandi, Giulia, Papalia, Rocco, Guaglianone, Salvatore, Costantini, Manuela, Cusumano, Giuseppe, Cigliana, Giovanni, Ascenzi, Paolo, Gallucci, Michele, Conti, Laura
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4324853/
https://www.ncbi.nlm.nih.gov/pubmed/25651917
http://dx.doi.org/10.1186/s13046-015-0127-8
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author Merola, Roberta
Tomao, Luigi
Antenucci, Anna
Sperduti, Isabella
Sentinelli, Steno
Masi, Serena
Mandoj, Chiara
Orlandi, Giulia
Papalia, Rocco
Guaglianone, Salvatore
Costantini, Manuela
Cusumano, Giuseppe
Cigliana, Giovanni
Ascenzi, Paolo
Gallucci, Michele
Conti, Laura
author_facet Merola, Roberta
Tomao, Luigi
Antenucci, Anna
Sperduti, Isabella
Sentinelli, Steno
Masi, Serena
Mandoj, Chiara
Orlandi, Giulia
Papalia, Rocco
Guaglianone, Salvatore
Costantini, Manuela
Cusumano, Giuseppe
Cigliana, Giovanni
Ascenzi, Paolo
Gallucci, Michele
Conti, Laura
author_sort Merola, Roberta
collection PubMed
description BACKGROUND: Prostate cancer (PCa) is the most common male cancer in Europe and the US. The early diagnosis relies on prostate specific antigen (PSA) serum test, even if it showed clear limits. Among the new tests currently under study, one of the most promising is the prostate cancer gene 3 (PCA3), a non-coding mRNA whose level increases up to 100 times in PCa tissues when compared to normal tissues. With the present study we contribute to the validation of the clinical utility of the PCA3 test and to the evaluation of its prognostic potential. METHODS: 407 Italian men, with two or more PCa risk factors and at least a previous negative biopsy, entering the Urology Unit of Regina Elena National Cancer Institute, were tested for PCA3, total PSA (tPSA) and free PSA (fPSA and f/tPSA) tests. Out of the 407 men enrolled, 195 were positive for PCa and 114 of them received an accurate staging with evaluation of the Gleason score (Gs). Then, the PCA3 score was correlated to biopsy outcome, and the diagnostic and prognostic utility were evaluated. RESULTS: Out of the 407 biopsies performed after the PCA3 test, 195 (48%) resulted positive for PCa; the PCA3 score was significantly higher in this population (p < 0.0001) differently to tPSA (p = 0.87). Moreover, the PCA3 test outperformed the f/tPSA (p = 0.01). The sensitivity (94.9) and specificity (60.1) of the PCA3 test showed a better balance for a threshold of 35 when compared to 20, even if the best result was achieved considering a cutoff of 51, with sensitivity and specificity of 82.1% and 79.3%, respectively. Finally, comparing values of the PCA3 test between two subgroups with increasing Gs (Gs ≤ 6 versus Gs ≥ 7) a significant association between PCA3 score and Gs was found (p = 0.02). CONCLUSIONS: The PCA3 test showed the best diagnostic performance when compared to tPSA and f/tPSA, facilitating the selection of high-risk patients that may benefit from the execution of a saturation prostatic biopsy. Moreover, the PCA3 test showed a prognostic value, as higher PCA3 score values are associated to a greater tumor aggressiveness.
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spelling pubmed-43248532015-02-12 PCA3 in prostate cancer and tumor aggressiveness detection on 407 high-risk patients: a National Cancer Institute experience Merola, Roberta Tomao, Luigi Antenucci, Anna Sperduti, Isabella Sentinelli, Steno Masi, Serena Mandoj, Chiara Orlandi, Giulia Papalia, Rocco Guaglianone, Salvatore Costantini, Manuela Cusumano, Giuseppe Cigliana, Giovanni Ascenzi, Paolo Gallucci, Michele Conti, Laura J Exp Clin Cancer Res Research Article BACKGROUND: Prostate cancer (PCa) is the most common male cancer in Europe and the US. The early diagnosis relies on prostate specific antigen (PSA) serum test, even if it showed clear limits. Among the new tests currently under study, one of the most promising is the prostate cancer gene 3 (PCA3), a non-coding mRNA whose level increases up to 100 times in PCa tissues when compared to normal tissues. With the present study we contribute to the validation of the clinical utility of the PCA3 test and to the evaluation of its prognostic potential. METHODS: 407 Italian men, with two or more PCa risk factors and at least a previous negative biopsy, entering the Urology Unit of Regina Elena National Cancer Institute, were tested for PCA3, total PSA (tPSA) and free PSA (fPSA and f/tPSA) tests. Out of the 407 men enrolled, 195 were positive for PCa and 114 of them received an accurate staging with evaluation of the Gleason score (Gs). Then, the PCA3 score was correlated to biopsy outcome, and the diagnostic and prognostic utility were evaluated. RESULTS: Out of the 407 biopsies performed after the PCA3 test, 195 (48%) resulted positive for PCa; the PCA3 score was significantly higher in this population (p < 0.0001) differently to tPSA (p = 0.87). Moreover, the PCA3 test outperformed the f/tPSA (p = 0.01). The sensitivity (94.9) and specificity (60.1) of the PCA3 test showed a better balance for a threshold of 35 when compared to 20, even if the best result was achieved considering a cutoff of 51, with sensitivity and specificity of 82.1% and 79.3%, respectively. Finally, comparing values of the PCA3 test between two subgroups with increasing Gs (Gs ≤ 6 versus Gs ≥ 7) a significant association between PCA3 score and Gs was found (p = 0.02). CONCLUSIONS: The PCA3 test showed the best diagnostic performance when compared to tPSA and f/tPSA, facilitating the selection of high-risk patients that may benefit from the execution of a saturation prostatic biopsy. Moreover, the PCA3 test showed a prognostic value, as higher PCA3 score values are associated to a greater tumor aggressiveness. BioMed Central 2015-02-06 /pmc/articles/PMC4324853/ /pubmed/25651917 http://dx.doi.org/10.1186/s13046-015-0127-8 Text en © Merola et al.; licensee BioMed Central. 2015 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly credited. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Research Article
Merola, Roberta
Tomao, Luigi
Antenucci, Anna
Sperduti, Isabella
Sentinelli, Steno
Masi, Serena
Mandoj, Chiara
Orlandi, Giulia
Papalia, Rocco
Guaglianone, Salvatore
Costantini, Manuela
Cusumano, Giuseppe
Cigliana, Giovanni
Ascenzi, Paolo
Gallucci, Michele
Conti, Laura
PCA3 in prostate cancer and tumor aggressiveness detection on 407 high-risk patients: a National Cancer Institute experience
title PCA3 in prostate cancer and tumor aggressiveness detection on 407 high-risk patients: a National Cancer Institute experience
title_full PCA3 in prostate cancer and tumor aggressiveness detection on 407 high-risk patients: a National Cancer Institute experience
title_fullStr PCA3 in prostate cancer and tumor aggressiveness detection on 407 high-risk patients: a National Cancer Institute experience
title_full_unstemmed PCA3 in prostate cancer and tumor aggressiveness detection on 407 high-risk patients: a National Cancer Institute experience
title_short PCA3 in prostate cancer and tumor aggressiveness detection on 407 high-risk patients: a National Cancer Institute experience
title_sort pca3 in prostate cancer and tumor aggressiveness detection on 407 high-risk patients: a national cancer institute experience
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4324853/
https://www.ncbi.nlm.nih.gov/pubmed/25651917
http://dx.doi.org/10.1186/s13046-015-0127-8
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