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Cochrane Database of Systematic Reviews

MRI pathway and TRUS‐guided biopsy for detecting clinically significant prostate cancer

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Información

DOI:
https://doi.org/10.1002/14651858.CD012663Copiar DOI
Base de datos:
  1. Cochrane Database of Systematic Reviews
Versión publicada:
  1. 24 mayo 2017see what's new
Tipo:
  1. Diagnostic
Etapa:
  1. Protocol
Grupo Editorial Cochrane:
  1. Grupo Cochrane de Urología

Copyright:
  1. Copyright © 2017 The Cochrane Collaboration. Published by John Wiley & Sons, Ltd.

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Autores

  • Frank‐Jan H Drost

    Correspondencia a: Department of Radiology and Nuclear Medicine, Erasmus University Medical Center, Rotterdam, Netherlands

    [email protected]

    [email protected]

    Department of Urology, Erasmus University Medical Center, Rotterdam, Netherlands

  • Monique J Roobol

    Department of Urology, Erasmus University Medical Center, Rotterdam, Netherlands

  • Daan Nieboer

    Department of Public Health, Erasmus University Medical Center, Rotterdam, Netherlands

  • Chris H Bangma

    Department of Urology, Erasmus University Medical Center, Rotterdam, Netherlands

  • Ewout W Steyerberg

    Department of Public Health, Erasmus University Medical Center, Rotterdam, Netherlands

  • M G Myriam Hunink

    Department of Radiology and Nuclear Medicine, Erasmus University Medical Center, Rotterdam, Netherlands

    Department of Epidemiology, Erasmus University Medical Center, Rotterdam, Netherlands

    Center for Health Decision Science, Harvard T.H. School of Public Health, Harvard University, Boston, USA

  • Ivo G Schoots

    Department of Radiology and Nuclear Medicine, Erasmus University Medical Center, Rotterdam, Netherlands

Contributions of authors

Frank‐Jan H Drost (FD), Ivo G Schoots (IS) and Monique J Roobol (MR) all initiated the review and wrote the protocol. FD and IS will conduct the literature search, review abstracts and full‐text studies for inclusion, and perform quality assessment, data extraction, analysis and writing of the review. MR will assist with the selection of studies and quality assessment and will contribute to the writing of the review. Daan Nieboer will perform the statistical analysis. Chris H Bangma, Ewout W Steyerberg and MG Myriam Hunink critically evaluated the protocol and will provide general advice on the review.

Declarations of interest

Ivo G Schoots: None known.

Monique J Roobol: None known.

Frank‐Jan Hendrik H Drost: None known.

Chris H Bangma: None known.

Ewout W Steyerberg reports the following relevant financial activities outside the submitted work: receives royalties from Springer for the textbook entitled Clinical Prediction Models.

MG Myriam Hunink reports the following relevant financial activities outside the submitted work: receives royalties from Cambridge University Press for the textbook entitled, Decision Making in Health and Medicine; received travel support from the European Society of Radiology (ESR), the International Society for Strategic Studies in Radiology (ISSSR), and the European Institute for Biomedical Imaging Research (EIBIR).

Acknowledgements

The authors thank Mr. WM Bramer, information specialist, Medical Library, Erasmus University Medical Center, Rotterdam, for conducting the systematic literature search.

Version history

Published

Title

Stage

Authors

Version

2019 Apr 25

Prostate MRI, with or without MRI‐targeted biopsy, and systematic biopsy for detecting prostate cancer

Review

Frank‐Jan H Drost, Daniël F Osses, Daan Nieboer, Ewout W Steyerberg, Chris H Bangma, Monique J Roobol, Ivo G Schoots

https://doi.org/10.1002/14651858.CD012663.pub2

2017 May 24

MRI pathway and TRUS‐guided biopsy for detecting clinically significant prostate cancer

Protocol

Frank‐Jan H Drost, Monique J Roobol, Daan Nieboer, Chris H Bangma, Ewout W Steyerberg, M G Myriam Hunink, Ivo G Schoots

https://doi.org/10.1002/14651858.CD012663

Keywords

MeSH

Medical Subject Headings Check Words

Humans; Male;

The MRI pathway comprises two components: MRI (suspicion score) and MRI‐targeted biopsy in the presence of suspicious lesions for clinically significant prostate cancer:a) MRI suspicion score: refers to only the first component of the MRI pathway. b) MRI±MRI‐TBx: refers to both components of the MRI pathway. Review design Meta‐analysis of studies reporting on:The MRI pathway and the reference standard: ·Comparison 1a: MRI suspicion score vs reference standard and all additional biopsies (e.g. MRI‐targeted biopsies). Comparison 1b: MRI±MRI‐TBx vs reference standard. TRUS‐guided biopsy and reference standard: ·Comparison 2 MRI pathway B) MRI±MRI‐TBx and TRUS‐guide biopsy: Comparison 3 A combination of all tests: Comparison 4: comparing both index tests, either directly with the reference standard or indirectly as a randomised trial of test accuracy.
Figuras y tablas -
Figure 1

The MRI pathway comprises two components: MRI (suspicion score) and MRI‐targeted biopsy in the presence of suspicious lesions for clinically significant prostate cancer:

  • a) MRI suspicion score: refers to only the first component of the MRI pathway.

  • b) MRI±MRI‐TBx: refers to both components of the MRI pathway.

Review design

Meta‐analysis of studies reporting on:

The MRI pathway and the reference standard: ·

  • Comparison 1a: MRI suspicion score vs reference standard and all additional biopsies (e.g. MRI‐targeted biopsies).

  • Comparison 1b: MRI±MRI‐TBx vs reference standard.

TRUS‐guided biopsy and reference standard: ·

  • Comparison 2

MRI pathway B) MRI±MRI‐TBx and TRUS‐guide biopsy:

  • Comparison 3

A combination of all tests:

  • Comparison 4: comparing both index tests, either directly with the reference standard or indirectly as a randomised trial of test accuracy.

Two‐by‐two contingency tables for target condition.Comparison 1a: MRI suspicion score vs reference standard (if MRI‐targeted biopsies are performed these will serve as additional reference biopsies).Comparison 1b: MRI±MRI‐TBx vs reference standard.Comparison 2: TRUS‐guided biopsy vs reference standard.Comparison 3: MRI±MRI‐TBx vs TRUS‐guided biopsy.For comparison 1b and comparison 3, a negative test can result in two ways:a negative MRI (thus no MRI‐targeted biopsies are taken). a positive MRI but negative MRI‐targeted biopsy result. Both negative outcomes should be merged, creating a two‐by‐two from a three‐by‐two contingency table (first and second column).In comparison 3 the TRUS‐guided biopsy is not a proper reference standard. Therefore we will focus on the number of cancers identified and the concordance and disconcordance between both index tests.TP = true positive; FP = false positive; TN = true negative; FN = false negative; Dposneg = Discordant MRI positive + targeted biopsies positive and TRUS‐guided biopsies negative; Dnegpos = Discordant MRI positive/negative + targeted biopsies negative and TRUS‐guided biopsies positive.
Figuras y tablas -
Figure 2

Two‐by‐two contingency tables for target condition.

Comparison 1a: MRI suspicion score vs reference standard (if MRI‐targeted biopsies are performed these will serve as additional reference biopsies).

Comparison 1b: MRI±MRI‐TBx vs reference standard.

Comparison 2: TRUS‐guided biopsy vs reference standard.

Comparison 3: MRI±MRI‐TBx vs TRUS‐guided biopsy.

For comparison 1b and comparison 3, a negative test can result in two ways:

  1. a negative MRI (thus no MRI‐targeted biopsies are taken).

  2. a positive MRI but negative MRI‐targeted biopsy result.

Both negative outcomes should be merged, creating a two‐by‐two from a three‐by‐two contingency table (first and second column).

In comparison 3 the TRUS‐guided biopsy is not a proper reference standard. Therefore we will focus on the number of cancers identified and the concordance and disconcordance between both index tests.

TP = true positive; FP = false positive; TN = true negative; FN = false negative; Dposneg = Discordant MRI positive + targeted biopsies positive and TRUS‐guided biopsies negative; Dnegpos = Discordant MRI positive/negative + targeted biopsies negative and TRUS‐guided biopsies positive.