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Clinically low‐risk prostate cancer: evaluation with transrectal doppler ultrasound and functional magnetic resonance imaging
OBJECTIVES: To evaluate transrectal ultrasound, amplitude Doppler ultrasound, conventional T(2)‐weighted magnetic resonance imaging, spectroscopy and dynamic contrast‐enhanced magnetic resonance imaging in localizing and locally staging low‐risk prostate cancer. INTRODUCTION: Prostate cancer has bee...
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Formato: | Texto |
Lenguaje: | English |
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Hospital das Clínicas da Faculdade de Medicina da Universidade de São Paulo
2011
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3044567/ https://www.ncbi.nlm.nih.gov/pubmed/21437432 http://dx.doi.org/10.1590/S1807-59322011000100006 |
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author | Novis, Maria Inês Baroni, Ronaldo Hueb de Oliveira Cerri, Luciana Mendes Mattedi, Romulo Loss Buchpiguel, Carlos Alberto |
author_facet | Novis, Maria Inês Baroni, Ronaldo Hueb de Oliveira Cerri, Luciana Mendes Mattedi, Romulo Loss Buchpiguel, Carlos Alberto |
author_sort | Novis, Maria Inês |
collection | PubMed |
description | OBJECTIVES: To evaluate transrectal ultrasound, amplitude Doppler ultrasound, conventional T(2)‐weighted magnetic resonance imaging, spectroscopy and dynamic contrast‐enhanced magnetic resonance imaging in localizing and locally staging low‐risk prostate cancer. INTRODUCTION: Prostate cancer has been diagnosed at earlier stages and the most accepted classification for low‐risk prostate cancer is based on clinical stage T1c or T2a, Gleason score ≤6, and prostate‐specific antigen (PSA) ≤10 ng/ml. METHODS: From 2005 to 2006, magnetic resonance imaging was performed in 42 patients, and transrectal ultrasound in 26 of these patients. Seven patients were excluded from the study. Mean patient age was 64.94 years and mean serum PSA was 6.05 ng/ml. The examinations were analyzed for tumor identification and location in prostate sextants, detection of extracapsular extension, and seminal vesicle invasion, using surgical pathology findings as the gold standard. RESULTS: Sixteen patients (45.7%) had pathologically proven organ‐confined disease, 11 (31.4%) had positive surgical margin, 8 (28.9%) had extracapsular extension, and 3 (8.6%) presented with extracapsular extension and seminal vesicle invasion. Sensitivity, specificity, positive predictive value (PPV), negative predictive value (NPV) and accuracy values for localizing low‐risk prostate cancer were 53.1%, 48.3%, 63.4%, 37.8% and 51.3% for transrectal ultrasound; 70.4%, 36.2%, 65.1%, 42.0% and 57.7% for amplitude Doppler ultrasound; 71.5%, 58.9%, 76.6%, 52.4% and 67.1% for magnetic resonance imaging; 70.4%, 58.7%, 78.4%, 48.2% and 66.7% for magnetic resonance spectroscopy; 67.2%, 65.7%, 79.3%, 50.6% and 66.7% for dynamic contrast‐enhanced magnetic resonance imaging, respectively. Sensitivity, specificity, PPV, NPV and accuracy values for detecting extracapsular extension were 33.3%, 92%, 14.3%, 97.2% and 89.7% for transrectal ultrasound and 50.0%, 77.6%, 13.7%, 95.6% and 75.7% for magnetic resonance imaging, respectively. For detecting seminal vesicle invasion, these values were 66.7%, 85.7%, 22.2%, 97.7% and 84.6% for transrectal ultrasound and 40.0%, 83.1%, 15.4%, 94.7% and 80.0% for magnetic resonance imaging. CONCLUSION: Although preliminary, our results suggest that imaging modalities have limited usefulness in localizing and locally staging clinically low‐risk prostate cancer. |
format | Text |
id | pubmed-3044567 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2011 |
publisher | Hospital das Clínicas da Faculdade de Medicina da Universidade de São Paulo |
record_format | MEDLINE/PubMed |
spelling | pubmed-30445672011-02-24 Clinically low‐risk prostate cancer: evaluation with transrectal doppler ultrasound and functional magnetic resonance imaging Novis, Maria Inês Baroni, Ronaldo Hueb de Oliveira Cerri, Luciana Mendes Mattedi, Romulo Loss Buchpiguel, Carlos Alberto Clinics (Sao Paulo) Clinical Science OBJECTIVES: To evaluate transrectal ultrasound, amplitude Doppler ultrasound, conventional T(2)‐weighted magnetic resonance imaging, spectroscopy and dynamic contrast‐enhanced magnetic resonance imaging in localizing and locally staging low‐risk prostate cancer. INTRODUCTION: Prostate cancer has been diagnosed at earlier stages and the most accepted classification for low‐risk prostate cancer is based on clinical stage T1c or T2a, Gleason score ≤6, and prostate‐specific antigen (PSA) ≤10 ng/ml. METHODS: From 2005 to 2006, magnetic resonance imaging was performed in 42 patients, and transrectal ultrasound in 26 of these patients. Seven patients were excluded from the study. Mean patient age was 64.94 years and mean serum PSA was 6.05 ng/ml. The examinations were analyzed for tumor identification and location in prostate sextants, detection of extracapsular extension, and seminal vesicle invasion, using surgical pathology findings as the gold standard. RESULTS: Sixteen patients (45.7%) had pathologically proven organ‐confined disease, 11 (31.4%) had positive surgical margin, 8 (28.9%) had extracapsular extension, and 3 (8.6%) presented with extracapsular extension and seminal vesicle invasion. Sensitivity, specificity, positive predictive value (PPV), negative predictive value (NPV) and accuracy values for localizing low‐risk prostate cancer were 53.1%, 48.3%, 63.4%, 37.8% and 51.3% for transrectal ultrasound; 70.4%, 36.2%, 65.1%, 42.0% and 57.7% for amplitude Doppler ultrasound; 71.5%, 58.9%, 76.6%, 52.4% and 67.1% for magnetic resonance imaging; 70.4%, 58.7%, 78.4%, 48.2% and 66.7% for magnetic resonance spectroscopy; 67.2%, 65.7%, 79.3%, 50.6% and 66.7% for dynamic contrast‐enhanced magnetic resonance imaging, respectively. Sensitivity, specificity, PPV, NPV and accuracy values for detecting extracapsular extension were 33.3%, 92%, 14.3%, 97.2% and 89.7% for transrectal ultrasound and 50.0%, 77.6%, 13.7%, 95.6% and 75.7% for magnetic resonance imaging, respectively. For detecting seminal vesicle invasion, these values were 66.7%, 85.7%, 22.2%, 97.7% and 84.6% for transrectal ultrasound and 40.0%, 83.1%, 15.4%, 94.7% and 80.0% for magnetic resonance imaging. CONCLUSION: Although preliminary, our results suggest that imaging modalities have limited usefulness in localizing and locally staging clinically low‐risk prostate cancer. Hospital das Clínicas da Faculdade de Medicina da Universidade de São Paulo 2011-01 /pmc/articles/PMC3044567/ /pubmed/21437432 http://dx.doi.org/10.1590/S1807-59322011000100006 Text en Copyright © 2011 Hospital das Clínicas da FMUSP http://creativecommons.org/licenses/by-nc/3.0/ 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 non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Clinical Science Novis, Maria Inês Baroni, Ronaldo Hueb de Oliveira Cerri, Luciana Mendes Mattedi, Romulo Loss Buchpiguel, Carlos Alberto Clinically low‐risk prostate cancer: evaluation with transrectal doppler ultrasound and functional magnetic resonance imaging |
title | Clinically low‐risk prostate cancer: evaluation with transrectal doppler ultrasound and functional magnetic resonance imaging |
title_full | Clinically low‐risk prostate cancer: evaluation with transrectal doppler ultrasound and functional magnetic resonance imaging |
title_fullStr | Clinically low‐risk prostate cancer: evaluation with transrectal doppler ultrasound and functional magnetic resonance imaging |
title_full_unstemmed | Clinically low‐risk prostate cancer: evaluation with transrectal doppler ultrasound and functional magnetic resonance imaging |
title_short | Clinically low‐risk prostate cancer: evaluation with transrectal doppler ultrasound and functional magnetic resonance imaging |
title_sort | clinically low‐risk prostate cancer: evaluation with transrectal doppler ultrasound and functional magnetic resonance imaging |
topic | Clinical Science |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3044567/ https://www.ncbi.nlm.nih.gov/pubmed/21437432 http://dx.doi.org/10.1590/S1807-59322011000100006 |
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