Prostate cancer detection at rebiopsy after an initial benign diagnosis: results using sextant extended prostate biopsy

Detalhes bibliográficos
Autor(a) principal: Leite, Katia Ramos Moreira
Data de Publicação: 2008
Outros Autores: Camara-Lopes, Luiz Heraldo, Cury, José, Dall'Oglio, Marcos F., Sañudo, Adriana, Srougi, Miguel
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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spelling 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
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