Optimizing Performance and Interpretation of Prostate Biopsy: A Critical Analysis of the Literature.

Standard

Optimizing Performance and Interpretation of Prostate Biopsy: A Critical Analysis of the Literature. / Chun, Felix; Epstein, Jonathan I; Ficarra, Vincenzo; Freedland, Stephen J; Montironi, Rodolfo; Montorsi, Francesco; Shariat, Shahrokh F; Schröder, Fritz H; Scattoni, Vincenzo.

In: EUR UROL, Vol. 58, No. 6, 6, 2010, p. 851-864.

Research output: SCORING: Contribution to journalSCORING: Journal articleResearchpeer-review

Harvard

Chun, F, Epstein, JI, Ficarra, V, Freedland, SJ, Montironi, R, Montorsi, F, Shariat, SF, Schröder, FH & Scattoni, V 2010, 'Optimizing Performance and Interpretation of Prostate Biopsy: A Critical Analysis of the Literature.', EUR UROL, vol. 58, no. 6, 6, pp. 851-864. <http://www.ncbi.nlm.nih.gov/pubmed/20884114?dopt=Citation>

APA

Chun, F., Epstein, J. I., Ficarra, V., Freedland, S. J., Montironi, R., Montorsi, F., Shariat, S. F., Schröder, F. H., & Scattoni, V. (2010). Optimizing Performance and Interpretation of Prostate Biopsy: A Critical Analysis of the Literature. EUR UROL, 58(6), 851-864. [6]. http://www.ncbi.nlm.nih.gov/pubmed/20884114?dopt=Citation

Vancouver

Chun F, Epstein JI, Ficarra V, Freedland SJ, Montironi R, Montorsi F et al. Optimizing Performance and Interpretation of Prostate Biopsy: A Critical Analysis of the Literature. EUR UROL. 2010;58(6):851-864. 6.

Bibtex

@article{e66491831d4f4128b3ceec89b3fccd91,
title = "Optimizing Performance and Interpretation of Prostate Biopsy: A Critical Analysis of the Literature.",
abstract = "CONTEXT: The number and location of biopsy cores and the interpretation of prostate biopsy in different clinical settings remain the subjects of continuing debate. OBJECTIVE: Our aim was to review the current evidence regarding the performance and interpretation of initial, repeat, and saturation prostatic biopsy. EVIDENCE ACQUISITION: A comprehensive Medline search was performed using the Medical Subject Heading search terms prostate biopsy, prostate cancer, detection, transrectal ultrasound (TRUS), nomogram, and diagnosis. Results were restricted to the English language, with preference given to those published within the last 3 yr. EVIDENCE SYNTHESIS: At initial biopsy, a minimum of 10 but not >18 systematic cores are recommended, with 14-18 cores in glands 50cm(3). Biopsies should be directed laterally, and transition zone (TZ) cores are not recommended in the initial biopsy setting. Further biopsy sets, either as an extended repeat or as a saturation biopsy ( 20 cores) including the TZ, are warranted in young and fit men with a persistent suspicion of prostate cancer. An immediate repeat biopsy is not indicated for prior high-grade prostatic intraepithelial neoplasia diagnosis given an adequate extended initial biopsy. Conversely, biopsies with atypical glands that are suspicious but not diagnostic of cancer should be repeated within 3-6 mo. Overall recommendations for further biopsy sets (a third set or more) cannot be made. Transrectal ultrasound-guided systematic biopsies represent the standard-of-care method of prostate sampling. However, transperineal biopsies are an up-to-standard alternative. CONCLUSIONS: The optimal prostatic biopsy regimen should be based on the individualized clinical setting of the patient and should follow the minimum standard requirements reported in this paper.",
author = "Felix Chun and Epstein, {Jonathan I} and Vincenzo Ficarra and Freedland, {Stephen J} and Rodolfo Montironi and Francesco Montorsi and Shariat, {Shahrokh F} and Schr{\"o}der, {Fritz H} and Vincenzo Scattoni",
year = "2010",
language = "Deutsch",
volume = "58",
pages = "851--864",
journal = "EUR UROL",
issn = "0302-2838",
publisher = "Elsevier",
number = "6",

}

RIS

TY - JOUR

T1 - Optimizing Performance and Interpretation of Prostate Biopsy: A Critical Analysis of the Literature.

AU - Chun, Felix

AU - Epstein, Jonathan I

AU - Ficarra, Vincenzo

AU - Freedland, Stephen J

AU - Montironi, Rodolfo

AU - Montorsi, Francesco

AU - Shariat, Shahrokh F

AU - Schröder, Fritz H

AU - Scattoni, Vincenzo

PY - 2010

Y1 - 2010

N2 - CONTEXT: The number and location of biopsy cores and the interpretation of prostate biopsy in different clinical settings remain the subjects of continuing debate. OBJECTIVE: Our aim was to review the current evidence regarding the performance and interpretation of initial, repeat, and saturation prostatic biopsy. EVIDENCE ACQUISITION: A comprehensive Medline search was performed using the Medical Subject Heading search terms prostate biopsy, prostate cancer, detection, transrectal ultrasound (TRUS), nomogram, and diagnosis. Results were restricted to the English language, with preference given to those published within the last 3 yr. EVIDENCE SYNTHESIS: At initial biopsy, a minimum of 10 but not >18 systematic cores are recommended, with 14-18 cores in glands 50cm(3). Biopsies should be directed laterally, and transition zone (TZ) cores are not recommended in the initial biopsy setting. Further biopsy sets, either as an extended repeat or as a saturation biopsy ( 20 cores) including the TZ, are warranted in young and fit men with a persistent suspicion of prostate cancer. An immediate repeat biopsy is not indicated for prior high-grade prostatic intraepithelial neoplasia diagnosis given an adequate extended initial biopsy. Conversely, biopsies with atypical glands that are suspicious but not diagnostic of cancer should be repeated within 3-6 mo. Overall recommendations for further biopsy sets (a third set or more) cannot be made. Transrectal ultrasound-guided systematic biopsies represent the standard-of-care method of prostate sampling. However, transperineal biopsies are an up-to-standard alternative. CONCLUSIONS: The optimal prostatic biopsy regimen should be based on the individualized clinical setting of the patient and should follow the minimum standard requirements reported in this paper.

AB - CONTEXT: The number and location of biopsy cores and the interpretation of prostate biopsy in different clinical settings remain the subjects of continuing debate. OBJECTIVE: Our aim was to review the current evidence regarding the performance and interpretation of initial, repeat, and saturation prostatic biopsy. EVIDENCE ACQUISITION: A comprehensive Medline search was performed using the Medical Subject Heading search terms prostate biopsy, prostate cancer, detection, transrectal ultrasound (TRUS), nomogram, and diagnosis. Results were restricted to the English language, with preference given to those published within the last 3 yr. EVIDENCE SYNTHESIS: At initial biopsy, a minimum of 10 but not >18 systematic cores are recommended, with 14-18 cores in glands 50cm(3). Biopsies should be directed laterally, and transition zone (TZ) cores are not recommended in the initial biopsy setting. Further biopsy sets, either as an extended repeat or as a saturation biopsy ( 20 cores) including the TZ, are warranted in young and fit men with a persistent suspicion of prostate cancer. An immediate repeat biopsy is not indicated for prior high-grade prostatic intraepithelial neoplasia diagnosis given an adequate extended initial biopsy. Conversely, biopsies with atypical glands that are suspicious but not diagnostic of cancer should be repeated within 3-6 mo. Overall recommendations for further biopsy sets (a third set or more) cannot be made. Transrectal ultrasound-guided systematic biopsies represent the standard-of-care method of prostate sampling. However, transperineal biopsies are an up-to-standard alternative. CONCLUSIONS: The optimal prostatic biopsy regimen should be based on the individualized clinical setting of the patient and should follow the minimum standard requirements reported in this paper.

M3 - SCORING: Zeitschriftenaufsatz

VL - 58

SP - 851

EP - 864

JO - EUR UROL

JF - EUR UROL

SN - 0302-2838

IS - 6

M1 - 6

ER -