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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...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Wolters Kluwer - Medknow
2023
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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. |
format | Online Article Text |
id | pubmed-10634460 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Wolters Kluwer - Medknow |
record_format | MEDLINE/PubMed |
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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