Comparison of cancer detection rates by transrectal prostate biopsy for prostate cancer using two different nomograms based on patient's age and prostate volume.

age cancer detection rate nomogram prostate cancer prostate volume transrectal prostate biopsy

Journal

Research and reports in urology
ISSN: 2253-2447
Titre abrégé: Res Rep Urol
Pays: England
ID NLM: 101576971

Informations de publication

Date de publication:
2019
Historique:
entrez: 3 4 2019
pubmed: 3 4 2019
medline: 3 4 2019
Statut: epublish

Résumé

The aim of this study is to evaluate the efficacy of two different Nara Urological Research and Treatment Group (NURTG) nomograms allocating 6-12 biopsy cores based on age and prostate volume. From April 2006 to July 2014, a total of 1,605 patients who underwent initial prostate biopsy were enrolled. Based on a nomogram taking the patient's age and prostate volume into consideration, 6-12 biopsy cores were allocated. Two types of nomogram were used, for the former group (before March 2009) and latter group (March 2009 onward). Cancer detection rates in all patients and those with prostate-specific antigen values in the gray zone (4.0-10 ng/mL) were compared. Predictive parameters for detection of prostate cancer in gray-zone patients were also investigated. The cancer detection rates in all patients and those in the gray zone were 48% and 38% in the former group and 54% and 41% in the latter group, respectively. The cancer detection rate in all patients was significantly higher in the latter group compared with the former group, but detection in gray-zone patients did not show a significant difference between the two groups ( The latter nomogram provided more acceptable detection rates of clinically significant and insignificant cancer than the former one, and we consider that an initial maximum 12-core transrectal ultrasound-guided needle biopsy may be sufficient for prostate cancer diagnosis.

Sections du résumé

BACKGROUND BACKGROUND
The aim of this study is to evaluate the efficacy of two different Nara Urological Research and Treatment Group (NURTG) nomograms allocating 6-12 biopsy cores based on age and prostate volume.
MATERIALS AND METHODS METHODS
From April 2006 to July 2014, a total of 1,605 patients who underwent initial prostate biopsy were enrolled. Based on a nomogram taking the patient's age and prostate volume into consideration, 6-12 biopsy cores were allocated. Two types of nomogram were used, for the former group (before March 2009) and latter group (March 2009 onward). Cancer detection rates in all patients and those with prostate-specific antigen values in the gray zone (4.0-10 ng/mL) were compared. Predictive parameters for detection of prostate cancer in gray-zone patients were also investigated.
RESULTS RESULTS
The cancer detection rates in all patients and those in the gray zone were 48% and 38% in the former group and 54% and 41% in the latter group, respectively. The cancer detection rate in all patients was significantly higher in the latter group compared with the former group, but detection in gray-zone patients did not show a significant difference between the two groups (
CONCLUSION CONCLUSIONS
The latter nomogram provided more acceptable detection rates of clinically significant and insignificant cancer than the former one, and we consider that an initial maximum 12-core transrectal ultrasound-guided needle biopsy may be sufficient for prostate cancer diagnosis.

Identifiants

pubmed: 30937289
doi: 10.2147/RRU.S193933
pii: rru-11-061
pmc: PMC6430996
doi:

Types de publication

Journal Article

Langues

eng

Pagination

61-68

Déclaration de conflit d'intérêts

Disclosure The authors report no conflicts of interest in this work.

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Auteurs

Shunta Hori (S)

Department of Urology, Nara Medical University, Kashihara, Nara 634-8522, Japan, sendo@naramed-u.ac.jp.

Nobumichi Tanaka (N)

Department of Urology, Nara Medical University, Kashihara, Nara 634-8522, Japan, sendo@naramed-u.ac.jp.

Yasushi Nakai (Y)

Department of Urology, Nara Medical University, Kashihara, Nara 634-8522, Japan, sendo@naramed-u.ac.jp.

Yosuke Morizawa (Y)

Department of Urology, Nara Medical University, Kashihara, Nara 634-8522, Japan, sendo@naramed-u.ac.jp.

Yoshihiro Tatsumi (Y)

Department of Urology, Nara Medical University, Kashihara, Nara 634-8522, Japan, sendo@naramed-u.ac.jp.

Makito Miyake (M)

Department of Urology, Nara Medical University, Kashihara, Nara 634-8522, Japan, sendo@naramed-u.ac.jp.

Satoshi Anai (S)

Department of Urology, Nara Medical University, Kashihara, Nara 634-8522, Japan, sendo@naramed-u.ac.jp.

Tomomi Fujii (T)

Department of Pathology, Nara Medical University, Kashihara, Nara 634-8522, Japan.

Noboru Konishi (N)

Department of Pathology, Nara Medical University, Kashihara, Nara 634-8522, Japan.

Yoshinori Nakagawa (Y)

Department of Urology, Yamatotakada Municipal Hospital, Yamatotakada, Nara 635-8501, Japan.

Syuya Hirao (S)

Department of Urology, Medical Corporation Katsurakai HIRAO Hospital, Kashihara, Nara 634-0076, Japan.

Kiyohide Fujimoto (K)

Department of Urology, Nara Medical University, Kashihara, Nara 634-8522, Japan, sendo@naramed-u.ac.jp.

Classifications MeSH