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Prostate-specific Antigen Density as a Proxy for Predicting Prostate Cancer Severity: Is There Any Difference between Systematic and Targeted Biopsy?

BACKGROUND: Prostate cancer screening with prostate-specific antigen (PSA) can result in unnecessary biopsies and overdiagnosis. Alternately, PSA density (PSAD) calculation may help support biopsy decisions; however, evidence of its usefulness is not concrete. OBJECTIVE: To evaluate the predictive v...

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Autores principales: Arafa, Mostafa A., Farhat, Karim Hamda, Rabah, Danny M., Khan, Farrukh K., Mokhtar, Alaa, Al-Taweel, Waleed
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Wolters Kluwer - Medknow 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10634460/
https://www.ncbi.nlm.nih.gov/pubmed/37970462
http://dx.doi.org/10.4103/sjmms.sjmms_49_23
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author Arafa, Mostafa A.
Farhat, Karim Hamda
Rabah, Danny M.
Khan, Farrukh K.
Mokhtar, Alaa
Al-Taweel, Waleed
author_facet Arafa, Mostafa A.
Farhat, Karim Hamda
Rabah, Danny M.
Khan, Farrukh K.
Mokhtar, Alaa
Al-Taweel, Waleed
author_sort Arafa, Mostafa A.
collection PubMed
description BACKGROUND: Prostate cancer screening with prostate-specific antigen (PSA) can result in unnecessary biopsies and overdiagnosis. Alternately, PSA density (PSAD) calculation may help support biopsy decisions; however, evidence of its usefulness is not concrete. OBJECTIVE: To evaluate the predictive value of PSAD for clinically significant prostate cancer detection by systematic and MRI-targeted biopsies. METHODS: This prospective study was conducted at two tertiary hospitals in Riyadh, Saudi Arabia, between December 2018 and November 2021. Patients suspected of prostate cancer were subjected to multi-parametric MRI, and for those with positive findings, systematic and targeted biopsies were performed. Clinically non-significant and significant prostate cancer cases were classified based on histopathology-defined ISUP grade or Gleason score. The PSAD was measured using the prostate volume determined by the MRI and categorized into ≤0.15, 0.16–0.20, and >0.20 ng/ml(2) subgroups. RESULTS: Systematic and targeted biopsies were carried out for 284 patients. The discriminant ability of PSAD is higher in MRI-targeted biopsy compared with systematic biopsy (AUC: 0.77 vs. 0.73). The highest sensitivity (97%) and specificity (87%) were detected at 0.07 ng/ml(2) in targeted biopsy. More than half of the clinically significant cases were detected in the >0.2 ng/ml(2) PSAD category (systematic: 52.4%; targeted: 51.1%). The CHAID methodology found that the probability of having clinically significant cancer (CSC) in patients with PSAD >0.15 ng/ml(2) was more than threefold than that in patients with PSAD ≤0.15 ng/ml(2) (64% vs. 20.2%). When considered by age, in PSAD ≤0.15 ng/ml(2) subgroup, the percentage of CSC detection rate increased from 20.2% to 24.6% in patients aged ≥60 years. CONCLUSION: PSAD has good discriminant power for predicting clinically significant prostate cancer. A cutoff of 0.07 ng/ml(2) should be adopted, but should be interpreted with caution and by considering other parameters such as age.
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spelling pubmed-106344602023-11-15 Prostate-specific Antigen Density as a Proxy for Predicting Prostate Cancer Severity: Is There Any Difference between Systematic and Targeted Biopsy? Arafa, Mostafa A. Farhat, Karim Hamda Rabah, Danny M. Khan, Farrukh K. Mokhtar, Alaa Al-Taweel, Waleed Saudi J Med Med Sci Original Article BACKGROUND: Prostate cancer screening with prostate-specific antigen (PSA) can result in unnecessary biopsies and overdiagnosis. Alternately, PSA density (PSAD) calculation may help support biopsy decisions; however, evidence of its usefulness is not concrete. OBJECTIVE: To evaluate the predictive value of PSAD for clinically significant prostate cancer detection by systematic and MRI-targeted biopsies. METHODS: This prospective study was conducted at two tertiary hospitals in Riyadh, Saudi Arabia, between December 2018 and November 2021. Patients suspected of prostate cancer were subjected to multi-parametric MRI, and for those with positive findings, systematic and targeted biopsies were performed. Clinically non-significant and significant prostate cancer cases were classified based on histopathology-defined ISUP grade or Gleason score. The PSAD was measured using the prostate volume determined by the MRI and categorized into ≤0.15, 0.16–0.20, and >0.20 ng/ml(2) subgroups. RESULTS: Systematic and targeted biopsies were carried out for 284 patients. The discriminant ability of PSAD is higher in MRI-targeted biopsy compared with systematic biopsy (AUC: 0.77 vs. 0.73). The highest sensitivity (97%) and specificity (87%) were detected at 0.07 ng/ml(2) in targeted biopsy. More than half of the clinically significant cases were detected in the >0.2 ng/ml(2) PSAD category (systematic: 52.4%; targeted: 51.1%). The CHAID methodology found that the probability of having clinically significant cancer (CSC) in patients with PSAD >0.15 ng/ml(2) was more than threefold than that in patients with PSAD ≤0.15 ng/ml(2) (64% vs. 20.2%). When considered by age, in PSAD ≤0.15 ng/ml(2) subgroup, the percentage of CSC detection rate increased from 20.2% to 24.6% in patients aged ≥60 years. CONCLUSION: PSAD has good discriminant power for predicting clinically significant prostate cancer. A cutoff of 0.07 ng/ml(2) should be adopted, but should be interpreted with caution and by considering other parameters such as age. Wolters Kluwer - Medknow 2023 2023-10-06 /pmc/articles/PMC10634460/ /pubmed/37970462 http://dx.doi.org/10.4103/sjmms.sjmms_49_23 Text en Copyright: © 2023 Saudi Journal of Medicine & Medical Sciences https://creativecommons.org/licenses/by-nc-sa/4.0/This is an open access journal, and articles are distributed under the terms of the Creative Commons Attribution-NonCommercial-ShareAlike 4.0 License, which allows others to remix, tweak, and build upon the work non-commercially, as long as appropriate credit is given and the new creations are licensed under the identical terms.
spellingShingle Original Article
Arafa, Mostafa A.
Farhat, Karim Hamda
Rabah, Danny M.
Khan, Farrukh K.
Mokhtar, Alaa
Al-Taweel, Waleed
Prostate-specific Antigen Density as a Proxy for Predicting Prostate Cancer Severity: Is There Any Difference between Systematic and Targeted Biopsy?
title Prostate-specific Antigen Density as a Proxy for Predicting Prostate Cancer Severity: Is There Any Difference between Systematic and Targeted Biopsy?
title_full Prostate-specific Antigen Density as a Proxy for Predicting Prostate Cancer Severity: Is There Any Difference between Systematic and Targeted Biopsy?
title_fullStr Prostate-specific Antigen Density as a Proxy for Predicting Prostate Cancer Severity: Is There Any Difference between Systematic and Targeted Biopsy?
title_full_unstemmed Prostate-specific Antigen Density as a Proxy for Predicting Prostate Cancer Severity: Is There Any Difference between Systematic and Targeted Biopsy?
title_short Prostate-specific Antigen Density as a Proxy for Predicting Prostate Cancer Severity: Is There Any Difference between Systematic and Targeted Biopsy?
title_sort prostate-specific antigen density as a proxy for predicting prostate cancer severity: is there any difference between systematic and targeted biopsy?
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10634460/
https://www.ncbi.nlm.nih.gov/pubmed/37970462
http://dx.doi.org/10.4103/sjmms.sjmms_49_23
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