Interactive, Up-to-date Meta-Analysis of MRI in the Management of Men with Suspected Prostate Cancer. Review uri icon

Overview

abstract

  • The aim of this study was to test an interactive up-to-date meta-analysis (iu-ma) of studies on MRI in the management of men with suspected prostate cancer. Based on the findings of recently published systematic reviews and meta-analyses, two freely accessible dynamic meta-analyses (https://iu-ma.org) were designed using the programming language R in combination with the package "shiny." The first iu-ma compares the performance of the MRI-stratified pathway and the systematic transrectal ultrasound-guided biopsy pathway for the detection of clinically significant prostate cancer, while the second iu-ma focuses on the use of biparametric versus multiparametric MRI for the diagnosis of prostate cancer. Our iu-mas allow for the effortless addition of new studies and data, thereby enabling physicians to keep track of the most recent scientific developments without having to resort to classical static meta-analyses that may become outdated in a short period of time. Furthermore, the iu-mas enable in-depth subgroup analyses by a wide variety of selectable parameters. Such an analysis is not only tailored to the needs of the reader but is also far more comprehensive than a classical meta-analysis. In that respect, following multiple subgroup analyses, we found that even for various subgroups, detection rates of prostate cancer are not different between biparametric and multiparametric MRI. Secondly, we could confirm the favorable influence of MRI biopsy stratification for multiple clinical scenarios. For the future, we envisage the use of this technology in addressing further clinical questions of other organ systems.

publication date

  • June 1, 2020

Research

keywords

  • Image-Guided Biopsy
  • Prostatic Neoplasms

Identity

PubMed Central ID

  • PMC7256175

Scopus Document Identifier

  • 85077607440

Digital Object Identifier (DOI)

  • 10.1016/j.ejrad.2017.07.016

PubMed ID

  • 31898035

Additional Document Info

volume

  • 33

issue

  • 3