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Transrectal ultrasound-guided prostate rebiopsy: How many core sampling should be applied to which patient?
BACKGROUND: We investigated the correlation between the sampled number of cores in rebiopsy and the cancer detection rate (CDR). MATERIALS AND METHODS: Two hundred and twelve patients with normal rectal examination who had undergone rebiopsy in the past 5 years were examined retrospectively. Moreove...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Medknow Publications & Media Pvt Ltd
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5791451/ https://www.ncbi.nlm.nih.gov/pubmed/29416269 http://dx.doi.org/10.4103/UA.UA_110_17 |
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author | Amasyalı, Akın Soner Yücetaş, Uğur Erkan, Erkan Demiray, Murat Karabay, Emre Murat, Cemalettin Toktaş, Gökhan Ünlüer, Erdinç |
author_facet | Amasyalı, Akın Soner Yücetaş, Uğur Erkan, Erkan Demiray, Murat Karabay, Emre Murat, Cemalettin Toktaş, Gökhan Ünlüer, Erdinç |
author_sort | Amasyalı, Akın Soner |
collection | PubMed |
description | BACKGROUND: We investigated the correlation between the sampled number of cores in rebiopsy and the cancer detection rate (CDR). MATERIALS AND METHODS: Two hundred and twelve patients with normal rectal examination who had undergone rebiopsy in the past 5 years were examined retrospectively. Moreover, 68% of them had undergone 12 cores (Group 1) while 32% had undergone 20 cores (Group 2). Both groups were compared with respect to the CDR. RESULTS: There was no difference between groups in terms of age, total prostate-specific antigen, and prostate volume (P > 0.05). Forty-one (19%) of 212 patients were diagnosed with cancer, and the CDR was significantly higher in Group 2 (30.9% vs. 13.9%, P = 0.004). This rate increased from 6.5% to 20% (P = 0.025) and from 0% to 33.3% (P = 0.023), respectively, with 12-core and 20-core rebiopsies in patients whose initial pathology indicated benign and high-grade prostatic intraepithelial neoplasia (HGPIN). Furthermore, cancer was detected in 24 (40%) of 60 patients who were diagnosed with atypical small acinar proliferation (ASAP) in the initial biopsy. However, despite being higher in 20-core biopsy group (47.6% vs. 35.9%), this was not statistically significant (P = 0.377). CONCLUSIONS: At least 20 cores should be sampled in rebiopsy, especially in the patients diagnosed with benign and HGPIN. However, we believe that standard systematic sampling will be sufficient for the patients diagnosed with ASAP. |
format | Online Article Text |
id | pubmed-5791451 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Medknow Publications & Media Pvt Ltd |
record_format | MEDLINE/PubMed |
spelling | pubmed-57914512018-02-07 Transrectal ultrasound-guided prostate rebiopsy: How many core sampling should be applied to which patient? Amasyalı, Akın Soner Yücetaş, Uğur Erkan, Erkan Demiray, Murat Karabay, Emre Murat, Cemalettin Toktaş, Gökhan Ünlüer, Erdinç Urol Ann Original Article BACKGROUND: We investigated the correlation between the sampled number of cores in rebiopsy and the cancer detection rate (CDR). MATERIALS AND METHODS: Two hundred and twelve patients with normal rectal examination who had undergone rebiopsy in the past 5 years were examined retrospectively. Moreover, 68% of them had undergone 12 cores (Group 1) while 32% had undergone 20 cores (Group 2). Both groups were compared with respect to the CDR. RESULTS: There was no difference between groups in terms of age, total prostate-specific antigen, and prostate volume (P > 0.05). Forty-one (19%) of 212 patients were diagnosed with cancer, and the CDR was significantly higher in Group 2 (30.9% vs. 13.9%, P = 0.004). This rate increased from 6.5% to 20% (P = 0.025) and from 0% to 33.3% (P = 0.023), respectively, with 12-core and 20-core rebiopsies in patients whose initial pathology indicated benign and high-grade prostatic intraepithelial neoplasia (HGPIN). Furthermore, cancer was detected in 24 (40%) of 60 patients who were diagnosed with atypical small acinar proliferation (ASAP) in the initial biopsy. However, despite being higher in 20-core biopsy group (47.6% vs. 35.9%), this was not statistically significant (P = 0.377). CONCLUSIONS: At least 20 cores should be sampled in rebiopsy, especially in the patients diagnosed with benign and HGPIN. However, we believe that standard systematic sampling will be sufficient for the patients diagnosed with ASAP. Medknow Publications & Media Pvt Ltd 2018 /pmc/articles/PMC5791451/ /pubmed/29416269 http://dx.doi.org/10.4103/UA.UA_110_17 Text en Copyright: © 2018 Urology Annals http://creativecommons.org/licenses/by-nc-sa/3.0 This is an open access article distributed under the terms of the Creative Commons Attribution-NonCommercial-ShareAlike 3.0 License, which allows others to remix, tweak, and build upon the work non-commercially, as long as the author is credited and the new creations are licensed under the identical terms. |
spellingShingle | Original Article Amasyalı, Akın Soner Yücetaş, Uğur Erkan, Erkan Demiray, Murat Karabay, Emre Murat, Cemalettin Toktaş, Gökhan Ünlüer, Erdinç Transrectal ultrasound-guided prostate rebiopsy: How many core sampling should be applied to which patient? |
title | Transrectal ultrasound-guided prostate rebiopsy: How many core sampling should be applied to which patient? |
title_full | Transrectal ultrasound-guided prostate rebiopsy: How many core sampling should be applied to which patient? |
title_fullStr | Transrectal ultrasound-guided prostate rebiopsy: How many core sampling should be applied to which patient? |
title_full_unstemmed | Transrectal ultrasound-guided prostate rebiopsy: How many core sampling should be applied to which patient? |
title_short | Transrectal ultrasound-guided prostate rebiopsy: How many core sampling should be applied to which patient? |
title_sort | transrectal ultrasound-guided prostate rebiopsy: how many core sampling should be applied to which patient? |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5791451/ https://www.ncbi.nlm.nih.gov/pubmed/29416269 http://dx.doi.org/10.4103/UA.UA_110_17 |
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