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Prostate cancer detection using multiparametric 3 – tesla MRI and fusion biopsy: preliminary results

OBJECTIVE: To evaluate the diagnostic efficacy of transrectal ultrasonography (US) biopsy with imaging fusion using multiparametric (mp) magnetic resonance imaging (MRI) in patients with suspicion of prostate cancer (PCa), with an emphasis on clinically significant tumors according to histological c...

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Autores principales: Mussi, Thais Caldara, Garcia, Rodrigo Gobbo, de Queiroz, Marcos Roberto Gomes, Lemos, Gustavo Caserta, Baroni, Ronaldo Hueb
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Sociedade Brasileira de Urologia 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5066885/
https://www.ncbi.nlm.nih.gov/pubmed/27532112
http://dx.doi.org/10.1590/S1677-5538.IBJU.2015.0204
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author Mussi, Thais Caldara
Garcia, Rodrigo Gobbo
de Queiroz, Marcos Roberto Gomes
Lemos, Gustavo Caserta
Baroni, Ronaldo Hueb
author_facet Mussi, Thais Caldara
Garcia, Rodrigo Gobbo
de Queiroz, Marcos Roberto Gomes
Lemos, Gustavo Caserta
Baroni, Ronaldo Hueb
author_sort Mussi, Thais Caldara
collection PubMed
description OBJECTIVE: To evaluate the diagnostic efficacy of transrectal ultrasonography (US) biopsy with imaging fusion using multiparametric (mp) magnetic resonance imaging (MRI) in patients with suspicion of prostate cancer (PCa), with an emphasis on clinically significant tumors according to histological criteria. MATERIALS AND METHODS: A total of 189 consecutive US/MRI fusion biopsies were performed obtaining systematic and guided samples of suspicious areas on mpMRI using a 3 Tesla magnet without endorectal coil. Clinical significance for prostate cancer was established based on Epstein criteria. RESULTS: In our casuistic, the average Gleason score was 7 and the average PSA was 5.0ng/mL. Of the 189 patients that received US/MRI biopsies, 110 (58.2%) were positive for PCa. Of those cases, 88 (80%) were clinically significant, accounting for 46.6% of all patients. We divided the MRI findings into 5 Likert scales of probability of having clinically significant PCa. The positivity of US/MRI biopsy for clinically significant PCa was 0%, 17.6% 23.5%, 53.4% and 84.4% for Likert scores 1, 2, 3, 4 and 5, respectively. There was a statistically significant difference in terms of biopsy results between different levels of suspicion on mpMRI and also when biopsy results were divided into groups of clinically non-significant versus clinically significant between different levels of suspicion on mpMRI (p-value <0.05 in both analyzes). CONCLUSION: We found that there is a significant difference in cancer detection using US/MRI fusion biopsy between low-probability and intermediate/high probability Likert scores using mpMRI.
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spelling pubmed-50668852016-10-20 Prostate cancer detection using multiparametric 3 – tesla MRI and fusion biopsy: preliminary results Mussi, Thais Caldara Garcia, Rodrigo Gobbo de Queiroz, Marcos Roberto Gomes Lemos, Gustavo Caserta Baroni, Ronaldo Hueb Int Braz J Urol Original Article OBJECTIVE: To evaluate the diagnostic efficacy of transrectal ultrasonography (US) biopsy with imaging fusion using multiparametric (mp) magnetic resonance imaging (MRI) in patients with suspicion of prostate cancer (PCa), with an emphasis on clinically significant tumors according to histological criteria. MATERIALS AND METHODS: A total of 189 consecutive US/MRI fusion biopsies were performed obtaining systematic and guided samples of suspicious areas on mpMRI using a 3 Tesla magnet without endorectal coil. Clinical significance for prostate cancer was established based on Epstein criteria. RESULTS: In our casuistic, the average Gleason score was 7 and the average PSA was 5.0ng/mL. Of the 189 patients that received US/MRI biopsies, 110 (58.2%) were positive for PCa. Of those cases, 88 (80%) were clinically significant, accounting for 46.6% of all patients. We divided the MRI findings into 5 Likert scales of probability of having clinically significant PCa. The positivity of US/MRI biopsy for clinically significant PCa was 0%, 17.6% 23.5%, 53.4% and 84.4% for Likert scores 1, 2, 3, 4 and 5, respectively. There was a statistically significant difference in terms of biopsy results between different levels of suspicion on mpMRI and also when biopsy results were divided into groups of clinically non-significant versus clinically significant between different levels of suspicion on mpMRI (p-value <0.05 in both analyzes). CONCLUSION: We found that there is a significant difference in cancer detection using US/MRI fusion biopsy between low-probability and intermediate/high probability Likert scores using mpMRI. Sociedade Brasileira de Urologia 2016 /pmc/articles/PMC5066885/ /pubmed/27532112 http://dx.doi.org/10.1590/S1677-5538.IBJU.2015.0204 Text en http://creativecommons.org/licenses/by/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Article
Mussi, Thais Caldara
Garcia, Rodrigo Gobbo
de Queiroz, Marcos Roberto Gomes
Lemos, Gustavo Caserta
Baroni, Ronaldo Hueb
Prostate cancer detection using multiparametric 3 – tesla MRI and fusion biopsy: preliminary results
title Prostate cancer detection using multiparametric 3 – tesla MRI and fusion biopsy: preliminary results
title_full Prostate cancer detection using multiparametric 3 – tesla MRI and fusion biopsy: preliminary results
title_fullStr Prostate cancer detection using multiparametric 3 – tesla MRI and fusion biopsy: preliminary results
title_full_unstemmed Prostate cancer detection using multiparametric 3 – tesla MRI and fusion biopsy: preliminary results
title_short Prostate cancer detection using multiparametric 3 – tesla MRI and fusion biopsy: preliminary results
title_sort prostate cancer detection using multiparametric 3 – tesla mri and fusion biopsy: preliminary results
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5066885/
https://www.ncbi.nlm.nih.gov/pubmed/27532112
http://dx.doi.org/10.1590/S1677-5538.IBJU.2015.0204
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