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Can Prostate-Specific Antigen Kinetics before Prostate Biopsy Predict the Malignant Potential of Prostate Cancer?

PURPOSE: To predict the malignant potential of prostate cancer (PCa) according to prostate-specific antigen velocity (PSAV), PSA density (PSAD), free/total PSA ratio (%fPSA), and digital rectal examination (DRE). MATERIALS AND METHODS: From January 2009 to December 2012, 548 adult male patients were...

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Autores principales: Kim, Sang Jin, Jeong, Tae Yoong, Yoo, Dae Seon, Park, Jinsung, Cho, Seok, Kang, Seok Ho, Lee, Sang Hyub, Jeon, Seung Hyun, Lee, Tchun Yong, Park, Sung Yul
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Yonsei University College of Medicine 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4630034/
https://www.ncbi.nlm.nih.gov/pubmed/26446628
http://dx.doi.org/10.3349/ymj.2015.56.6.1492
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author Kim, Sang Jin
Jeong, Tae Yoong
Yoo, Dae Seon
Park, Jinsung
Cho, Seok
Kang, Seok Ho
Lee, Sang Hyub
Jeon, Seung Hyun
Lee, Tchun Yong
Park, Sung Yul
author_facet Kim, Sang Jin
Jeong, Tae Yoong
Yoo, Dae Seon
Park, Jinsung
Cho, Seok
Kang, Seok Ho
Lee, Sang Hyub
Jeon, Seung Hyun
Lee, Tchun Yong
Park, Sung Yul
author_sort Kim, Sang Jin
collection PubMed
description PURPOSE: To predict the malignant potential of prostate cancer (PCa) according to prostate-specific antigen velocity (PSAV), PSA density (PSAD), free/total PSA ratio (%fPSA), and digital rectal examination (DRE). MATERIALS AND METHODS: From January 2009 to December 2012, 548 adult male patients were diagnosed with PCa by prostate biopsy at four hospitals in Korea. We retrospectively analyzed 155 adult male patients with an initial PSA level ≤10 ng/mL and whose PSA levels had been checked more than two times at least 6 months before they had been diagnosed with PCa, with test intervals of more than 3 months. Patients with a urinary tract infection, and patients who had previously undergone cystoscopy or surgery of the prostate were excluded. We separated patients into two groups according to Gleason sum [Gleason sum ≤7 (n=134) or Gleason sum ≥8 (n=21)] and the presence of extracapsular invasion [organ confined (n=129) or extracapsular invasion (n=26)]. Differences between the groups were compared. RESULTS: The group with a Gleason sum ≥8 or extracapsular invasion of PCa showed high PSAV and significantly lower %fPSA. There were no significant differences in PSAD and the presence of an abnormality on DRE between two groups. CONCLUSION: In PCa patients treated with other therapies besides prostatectomy, a high PSA velocity and a low %fPSA may predict high grade PCa with a Gleason sum ≥8 or the presence of extracapsular invasion.
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spelling pubmed-46300342015-11-04 Can Prostate-Specific Antigen Kinetics before Prostate Biopsy Predict the Malignant Potential of Prostate Cancer? Kim, Sang Jin Jeong, Tae Yoong Yoo, Dae Seon Park, Jinsung Cho, Seok Kang, Seok Ho Lee, Sang Hyub Jeon, Seung Hyun Lee, Tchun Yong Park, Sung Yul Yonsei Med J Original Article PURPOSE: To predict the malignant potential of prostate cancer (PCa) according to prostate-specific antigen velocity (PSAV), PSA density (PSAD), free/total PSA ratio (%fPSA), and digital rectal examination (DRE). MATERIALS AND METHODS: From January 2009 to December 2012, 548 adult male patients were diagnosed with PCa by prostate biopsy at four hospitals in Korea. We retrospectively analyzed 155 adult male patients with an initial PSA level ≤10 ng/mL and whose PSA levels had been checked more than two times at least 6 months before they had been diagnosed with PCa, with test intervals of more than 3 months. Patients with a urinary tract infection, and patients who had previously undergone cystoscopy or surgery of the prostate were excluded. We separated patients into two groups according to Gleason sum [Gleason sum ≤7 (n=134) or Gleason sum ≥8 (n=21)] and the presence of extracapsular invasion [organ confined (n=129) or extracapsular invasion (n=26)]. Differences between the groups were compared. RESULTS: The group with a Gleason sum ≥8 or extracapsular invasion of PCa showed high PSAV and significantly lower %fPSA. There were no significant differences in PSAD and the presence of an abnormality on DRE between two groups. CONCLUSION: In PCa patients treated with other therapies besides prostatectomy, a high PSA velocity and a low %fPSA may predict high grade PCa with a Gleason sum ≥8 or the presence of extracapsular invasion. Yonsei University College of Medicine 2015-11-01 2015-09-25 /pmc/articles/PMC4630034/ /pubmed/26446628 http://dx.doi.org/10.3349/ymj.2015.56.6.1492 Text en © Copyright: Yonsei University College of Medicine 2015 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 Original Article
Kim, Sang Jin
Jeong, Tae Yoong
Yoo, Dae Seon
Park, Jinsung
Cho, Seok
Kang, Seok Ho
Lee, Sang Hyub
Jeon, Seung Hyun
Lee, Tchun Yong
Park, Sung Yul
Can Prostate-Specific Antigen Kinetics before Prostate Biopsy Predict the Malignant Potential of Prostate Cancer?
title Can Prostate-Specific Antigen Kinetics before Prostate Biopsy Predict the Malignant Potential of Prostate Cancer?
title_full Can Prostate-Specific Antigen Kinetics before Prostate Biopsy Predict the Malignant Potential of Prostate Cancer?
title_fullStr Can Prostate-Specific Antigen Kinetics before Prostate Biopsy Predict the Malignant Potential of Prostate Cancer?
title_full_unstemmed Can Prostate-Specific Antigen Kinetics before Prostate Biopsy Predict the Malignant Potential of Prostate Cancer?
title_short Can Prostate-Specific Antigen Kinetics before Prostate Biopsy Predict the Malignant Potential of Prostate Cancer?
title_sort can prostate-specific antigen kinetics before prostate biopsy predict the malignant potential of prostate cancer?
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4630034/
https://www.ncbi.nlm.nih.gov/pubmed/26446628
http://dx.doi.org/10.3349/ymj.2015.56.6.1492
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