Prostate cancer detection at rebiopsy after an initial benign diagnosis: results using sextant extended prostate biopsy
Autor(a) principal: | |
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Data de Publicação: | 2008 |
Outros Autores: | , , , , |
Tipo de documento: | Artigo |
Idioma: | eng |
Título da fonte: | Clinics |
Texto Completo: | https://www.revistas.usp.br/clinics/article/view/17803 |
Resumo: | INTRODUCTION: Sextant prostate biopsy remains the standard technique for the detection of prostate cancer. It is well known that after a diagnosis of small acinar proliferation (ASAP) or high grade prostate intraepithelial neoplasia (HGPIN), the possibility of finding cancer is approximately 40% and 30%, respectively. OBJECTIVE: We aim to analyze follow-up biopsies on patients who initially received a benign diagnosis after exclusion of HGPIN and ASAP. METHODS: From July 2000 to December 2003, 1177 patients were submitted to sextant extended prostate biopsy in our hospital. The mean patient age was 65.5 years old, and the median number of fragments collected at biopsy was 13. HGPIN and ASAP were excluded from our study. We only considered patients who had a diagnosis of benign at the first biopsy and were subjected to rebiopsies up until May 2005 because of a maintained suspicion of cancer. RESULTS: Cancer was initially detected in 524 patients (44.5%), and the diagnosis was benign in 415 (35.3%). Rebiopsy was indicated for 76 of the latter patients (18.3%) because of a persistent suspicion of cancer. Eight cases of adenocarcinoma (10.5%) were detected, six (75%) at the first rebiopsy. Six patients were submitted to radical prostatectomy, and all tumors were considered clinically significant. CONCLUSION: Our data indicate that in extended prostate biopsy, the first biopsy detects more cancer, and the first, second, and third rebiopsies after an initial benign diagnosis succeed in finding cancer in 7.9% (6/55), 5.9% (1/15) and 20% (1/4) of patients, respectively. |
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Clinics |
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Prostate cancer detection at rebiopsy after an initial benign diagnosis: results using sextant extended prostate biopsy ProstateCancerAdenocarcinomaBiopsyBenignProstatic neoplasms INTRODUCTION: Sextant prostate biopsy remains the standard technique for the detection of prostate cancer. It is well known that after a diagnosis of small acinar proliferation (ASAP) or high grade prostate intraepithelial neoplasia (HGPIN), the possibility of finding cancer is approximately 40% and 30%, respectively. OBJECTIVE: We aim to analyze follow-up biopsies on patients who initially received a benign diagnosis after exclusion of HGPIN and ASAP. METHODS: From July 2000 to December 2003, 1177 patients were submitted to sextant extended prostate biopsy in our hospital. The mean patient age was 65.5 years old, and the median number of fragments collected at biopsy was 13. HGPIN and ASAP were excluded from our study. We only considered patients who had a diagnosis of benign at the first biopsy and were subjected to rebiopsies up until May 2005 because of a maintained suspicion of cancer. RESULTS: Cancer was initially detected in 524 patients (44.5%), and the diagnosis was benign in 415 (35.3%). Rebiopsy was indicated for 76 of the latter patients (18.3%) because of a persistent suspicion of cancer. Eight cases of adenocarcinoma (10.5%) were detected, six (75%) at the first rebiopsy. Six patients were submitted to radical prostatectomy, and all tumors were considered clinically significant. CONCLUSION: Our data indicate that in extended prostate biopsy, the first biopsy detects more cancer, and the first, second, and third rebiopsies after an initial benign diagnosis succeed in finding cancer in 7.9% (6/55), 5.9% (1/15) and 20% (1/4) of patients, respectively. Hospital das Clínicas, Faculdade de Medicina, Universidade de São Paulo2008-01-01info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersionapplication/pdfhttps://www.revistas.usp.br/clinics/article/view/1780310.1590/S1807-59322008000300009Clinics; Vol. 63 No. 3 (2008); 339-342 Clinics; v. 63 n. 3 (2008); 339-342 Clinics; Vol. 63 Núm. 3 (2008); 339-342 1980-53221807-5932reponame:Clinicsinstname:Universidade de São Paulo (USP)instacron:USPenghttps://www.revistas.usp.br/clinics/article/view/17803/19868Leite, Katia Ramos MoreiraCamara-Lopes, Luiz HeraldoCury, JoséDall'Oglio, Marcos F.Sañudo, AdrianaSrougi, Miguelinfo:eu-repo/semantics/openAccess2012-05-22T18:34:36Zoai:revistas.usp.br:article/17803Revistahttps://www.revistas.usp.br/clinicsPUBhttps://www.revistas.usp.br/clinics/oai||clinics@hc.fm.usp.br1980-53221807-5932opendoar:2012-05-22T18:34:36Clinics - Universidade de São Paulo (USP)false |
dc.title.none.fl_str_mv |
Prostate cancer detection at rebiopsy after an initial benign diagnosis: results using sextant extended prostate biopsy |
title |
Prostate cancer detection at rebiopsy after an initial benign diagnosis: results using sextant extended prostate biopsy |
spellingShingle |
Prostate cancer detection at rebiopsy after an initial benign diagnosis: results using sextant extended prostate biopsy Leite, Katia Ramos Moreira Prostate Cancer Adenocarcinoma Biopsy Benign Prostatic neoplasms |
title_short |
Prostate cancer detection at rebiopsy after an initial benign diagnosis: results using sextant extended prostate biopsy |
title_full |
Prostate cancer detection at rebiopsy after an initial benign diagnosis: results using sextant extended prostate biopsy |
title_fullStr |
Prostate cancer detection at rebiopsy after an initial benign diagnosis: results using sextant extended prostate biopsy |
title_full_unstemmed |
Prostate cancer detection at rebiopsy after an initial benign diagnosis: results using sextant extended prostate biopsy |
title_sort |
Prostate cancer detection at rebiopsy after an initial benign diagnosis: results using sextant extended prostate biopsy |
author |
Leite, Katia Ramos Moreira |
author_facet |
Leite, Katia Ramos Moreira Camara-Lopes, Luiz Heraldo Cury, José Dall'Oglio, Marcos F. Sañudo, Adriana Srougi, Miguel |
author_role |
author |
author2 |
Camara-Lopes, Luiz Heraldo Cury, José Dall'Oglio, Marcos F. Sañudo, Adriana Srougi, Miguel |
author2_role |
author author author author author |
dc.contributor.author.fl_str_mv |
Leite, Katia Ramos Moreira Camara-Lopes, Luiz Heraldo Cury, José Dall'Oglio, Marcos F. Sañudo, Adriana Srougi, Miguel |
dc.subject.por.fl_str_mv |
Prostate Cancer Adenocarcinoma Biopsy Benign Prostatic neoplasms |
topic |
Prostate Cancer Adenocarcinoma Biopsy Benign Prostatic neoplasms |
description |
INTRODUCTION: Sextant prostate biopsy remains the standard technique for the detection of prostate cancer. It is well known that after a diagnosis of small acinar proliferation (ASAP) or high grade prostate intraepithelial neoplasia (HGPIN), the possibility of finding cancer is approximately 40% and 30%, respectively. OBJECTIVE: We aim to analyze follow-up biopsies on patients who initially received a benign diagnosis after exclusion of HGPIN and ASAP. METHODS: From July 2000 to December 2003, 1177 patients were submitted to sextant extended prostate biopsy in our hospital. The mean patient age was 65.5 years old, and the median number of fragments collected at biopsy was 13. HGPIN and ASAP were excluded from our study. We only considered patients who had a diagnosis of benign at the first biopsy and were subjected to rebiopsies up until May 2005 because of a maintained suspicion of cancer. RESULTS: Cancer was initially detected in 524 patients (44.5%), and the diagnosis was benign in 415 (35.3%). Rebiopsy was indicated for 76 of the latter patients (18.3%) because of a persistent suspicion of cancer. Eight cases of adenocarcinoma (10.5%) were detected, six (75%) at the first rebiopsy. Six patients were submitted to radical prostatectomy, and all tumors were considered clinically significant. CONCLUSION: Our data indicate that in extended prostate biopsy, the first biopsy detects more cancer, and the first, second, and third rebiopsies after an initial benign diagnosis succeed in finding cancer in 7.9% (6/55), 5.9% (1/15) and 20% (1/4) of patients, respectively. |
publishDate |
2008 |
dc.date.none.fl_str_mv |
2008-01-01 |
dc.type.driver.fl_str_mv |
info:eu-repo/semantics/article info:eu-repo/semantics/publishedVersion |
format |
article |
status_str |
publishedVersion |
dc.identifier.uri.fl_str_mv |
https://www.revistas.usp.br/clinics/article/view/17803 10.1590/S1807-59322008000300009 |
url |
https://www.revistas.usp.br/clinics/article/view/17803 |
identifier_str_mv |
10.1590/S1807-59322008000300009 |
dc.language.iso.fl_str_mv |
eng |
language |
eng |
dc.relation.none.fl_str_mv |
https://www.revistas.usp.br/clinics/article/view/17803/19868 |
dc.rights.driver.fl_str_mv |
info:eu-repo/semantics/openAccess |
eu_rights_str_mv |
openAccess |
dc.format.none.fl_str_mv |
application/pdf |
dc.publisher.none.fl_str_mv |
Hospital das Clínicas, Faculdade de Medicina, Universidade de São Paulo |
publisher.none.fl_str_mv |
Hospital das Clínicas, Faculdade de Medicina, Universidade de São Paulo |
dc.source.none.fl_str_mv |
Clinics; Vol. 63 No. 3 (2008); 339-342 Clinics; v. 63 n. 3 (2008); 339-342 Clinics; Vol. 63 Núm. 3 (2008); 339-342 1980-5322 1807-5932 reponame:Clinics instname:Universidade de São Paulo (USP) instacron:USP |
instname_str |
Universidade de São Paulo (USP) |
instacron_str |
USP |
institution |
USP |
reponame_str |
Clinics |
collection |
Clinics |
repository.name.fl_str_mv |
Clinics - Universidade de São Paulo (USP) |
repository.mail.fl_str_mv |
||clinics@hc.fm.usp.br |
_version_ |
1800222753897316352 |