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The characteristics and spatial distributions of initially missed and rebiopsy-detected prostate cancers
PURPOSE: The purpose of this study was to analyze the characteristics of initially missed and rebiopsy-detected prostate cancers following 12-core transrectal biopsy. METHODS: A total of 45 patients with prostate cancers detected on rebiopsy and 45 patients with prostate cancers initially detected o...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Korean Society of Ultrasound in Medicine
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4939716/ https://www.ncbi.nlm.nih.gov/pubmed/27048261 http://dx.doi.org/10.14366/usg.15065 |
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author | You, Myung-Won Kim, Mi-Hyun Kim, Jeong Kon Cho, Kyoung-Sik |
author_facet | You, Myung-Won Kim, Mi-Hyun Kim, Jeong Kon Cho, Kyoung-Sik |
author_sort | You, Myung-Won |
collection | PubMed |
description | PURPOSE: The purpose of this study was to analyze the characteristics of initially missed and rebiopsy-detected prostate cancers following 12-core transrectal biopsy. METHODS: A total of 45 patients with prostate cancers detected on rebiopsy and 45 patients with prostate cancers initially detected on transrectal ultrasound-guided biopsy were included in the study. For result analysis, the prostate was divided into six compartments, and the cancer positive rates, estimated tumor burden, and agreement rates between biopsy and surgical specimens, along with clinical data, were evaluated. RESULTS: The largest mean tumor burden was located in the medial apex in both groups. There were significantly more tumors in this location in the rebiopsy group (44.9%) than in the control group (30.1%, P=0.015). The overall sensitivity of biopsy was significantly lower in the rebiopsy group (22.5% vs. 43.4%, P<0.001). The agreement rate of cancer positive cores between biopsy and surgical specimens was significantly lower in the medial apex in the rebiopsy group compared with that of the control group (50.0% vs. 65.6%, P=0.035). The cancer positive rates of target biopsy cores and premalignant lesions in the rebiopsy group were 63.1% and 42.3%, respectively. CONCLUSION: Rebiopsy-detected prostate cancers showed different spatial distribution and lower cancer detection rate of biopsy cores compared with initially diagnosed cancers. To overcome lower cancer detection rate, target biopsy of abnormal sonographic findings, premalignant lesions and medial apex which revealed larger tumor burden would be recommended when performing rebiopsy. |
format | Online Article Text |
id | pubmed-4939716 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Korean Society of Ultrasound in Medicine |
record_format | MEDLINE/PubMed |
spelling | pubmed-49397162016-07-12 The characteristics and spatial distributions of initially missed and rebiopsy-detected prostate cancers You, Myung-Won Kim, Mi-Hyun Kim, Jeong Kon Cho, Kyoung-Sik Ultrasonography Original Article PURPOSE: The purpose of this study was to analyze the characteristics of initially missed and rebiopsy-detected prostate cancers following 12-core transrectal biopsy. METHODS: A total of 45 patients with prostate cancers detected on rebiopsy and 45 patients with prostate cancers initially detected on transrectal ultrasound-guided biopsy were included in the study. For result analysis, the prostate was divided into six compartments, and the cancer positive rates, estimated tumor burden, and agreement rates between biopsy and surgical specimens, along with clinical data, were evaluated. RESULTS: The largest mean tumor burden was located in the medial apex in both groups. There were significantly more tumors in this location in the rebiopsy group (44.9%) than in the control group (30.1%, P=0.015). The overall sensitivity of biopsy was significantly lower in the rebiopsy group (22.5% vs. 43.4%, P<0.001). The agreement rate of cancer positive cores between biopsy and surgical specimens was significantly lower in the medial apex in the rebiopsy group compared with that of the control group (50.0% vs. 65.6%, P=0.035). The cancer positive rates of target biopsy cores and premalignant lesions in the rebiopsy group were 63.1% and 42.3%, respectively. CONCLUSION: Rebiopsy-detected prostate cancers showed different spatial distribution and lower cancer detection rate of biopsy cores compared with initially diagnosed cancers. To overcome lower cancer detection rate, target biopsy of abnormal sonographic findings, premalignant lesions and medial apex which revealed larger tumor burden would be recommended when performing rebiopsy. Korean Society of Ultrasound in Medicine 2016-07 2016-02-12 /pmc/articles/PMC4939716/ /pubmed/27048261 http://dx.doi.org/10.14366/usg.15065 Text en Copyright © 2016 Korean Society of Ultrasound in Medicine (KSUM) This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/3.0/) which permits unrestricted noncommercial use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Original Article You, Myung-Won Kim, Mi-Hyun Kim, Jeong Kon Cho, Kyoung-Sik The characteristics and spatial distributions of initially missed and rebiopsy-detected prostate cancers |
title | The characteristics and spatial distributions of initially missed and rebiopsy-detected prostate cancers |
title_full | The characteristics and spatial distributions of initially missed and rebiopsy-detected prostate cancers |
title_fullStr | The characteristics and spatial distributions of initially missed and rebiopsy-detected prostate cancers |
title_full_unstemmed | The characteristics and spatial distributions of initially missed and rebiopsy-detected prostate cancers |
title_short | The characteristics and spatial distributions of initially missed and rebiopsy-detected prostate cancers |
title_sort | characteristics and spatial distributions of initially missed and rebiopsy-detected prostate cancers |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4939716/ https://www.ncbi.nlm.nih.gov/pubmed/27048261 http://dx.doi.org/10.14366/usg.15065 |
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