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Tytuł pozycji:

Risk Stratification of Prostate Cancer According to PI-RADS® Version 2 Categories: Meta-Analysis for Prospective Studies.

Tytuł:
Risk Stratification of Prostate Cancer According to PI-RADS® Version 2 Categories: Meta-Analysis for Prospective Studies.
Autorzy:
Park KJ; Department of Radiology and Research Institute of Radiology, University of Ulsan College of Medicine, Asan Medical Center, Seoul, Republic of Korea.
Choi SH; Department of Radiology and Research Institute of Radiology, University of Ulsan College of Medicine, Asan Medical Center, Seoul, Republic of Korea.
Lee JS; Department of Clinical Epidemiology and Biostatistics, Asan Medical Center, University of Ulsan College of Medicine, Seoul, Republic of Korea.; Clinical Research Center, Asan Institute for Life Sciences, Asan Medical Center, University of Ulsan College of Medicine, Seoul, Korea.
Kim JK; Department of Radiology and Research Institute of Radiology, University of Ulsan College of Medicine, Asan Medical Center, Seoul, Republic of Korea.
Kim MH; Department of Radiology and Research Institute of Radiology, University of Ulsan College of Medicine, Asan Medical Center, Seoul, Republic of Korea.
Jeong IG; Department of Urology, University of Ulsan College of Medicine, Asan Medical Center, Seoul, Republic of Korea.
Źródło:
The Journal of urology [J Urol] 2020 Dec; Vol. 204 (6), pp. 1141-1149. Date of Electronic Publication: 2020 Jul 27.
Typ publikacji:
Journal Article; Meta-Analysis
Język:
English
Imprint Name(s):
Publication: 2019- : [Philadelphia, PA] : Wolters Kluwer
Original Publication: Baltimore : Lippincott Williams & Wilkins
MeSH Terms:
Magnetic Resonance Imaging, Interventional*
Prostate/*pathology
Prostatic Neoplasms/*diagnosis
Biopsy, Large-Core Needle/methods ; Critical Pathways ; Feasibility Studies ; Humans ; Image-Guided Biopsy/methods ; Male ; Prospective Studies ; Prostate/diagnostic imaging ; Prostatic Neoplasms/epidemiology ; Prostatic Neoplasms/pathology ; Risk Assessment/methods ; Ultrasonography, Interventional
Contributed Indexing:
Keywords: magnetic resonance imaging; prostate; prostatic neoplasms
Entry Date(s):
Date Created: 20200728 Date Completed: 20201124 Latest Revision: 20201124
Update Code:
20240104
DOI:
10.1097/JU.0000000000001306
PMID:
32716687
Czasopismo naukowe
Purpose: The Prostate Imaging Reporting and Data System (PI-RADS) version 2 (v2) categorizes the likelihood of clinically significant prostate cancer on magnetic resonance imaging and determines the diagnostic pathway. We determined clinically significant prostate cancer and all prostate cancer detection rates in each PI-RADS v2 category.
Materials and Methods: MEDLINE®, EMBASE® and Cochrane databases were searched for prospective studies reporting the detection rates of clinically significant prostate cancer or all prostate cancer. Random effects models were used to determine pooled detection rates of clinically significant prostate cancer and all prostate cancer for each PI-RADS category. The risk of bias was assessed with the Quality Assessment of Diagnostic Accuracy Studies-2. Meta-regression analysis was performed to identify factors affecting study heterogeneity.
Results: Thirteen prospective studies including 4,265 men who underwent magnetic resonance imaging targeted biopsy and/or systematic biopsy for a PI-RADS v2 category 3 or greater, or systematic biopsy for PI-RADS 1-2 were included. The pooled detection rates of clinically significant prostate cancer monotonically increased for each PI-RADS v2 category, ie 4% (95% CI 2-8) for category 1-2, 17% (95% CI 13-21) for category 3, 46% (95% CI 38-55) for category 4 and 75% (95% CI 73-78) for category 5. Substantial study heterogeneity was noted in clinically significant prostate cancer detection rates for categories 1-2 and 4, which were significantly affected by study subject selection (biopsy naïve patients only or not) and studies with a high risk of bias.
Conclusions: PI-RADS v2 can be useful for the stratification of the risk of clinically significant prostate cancer in patients at risk for prostate cancer but the limitations in category 4 still remain.

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