Evaluation of the PI-RADS v2.1 Score Using Multiple Readers
NCT ID: NCT04299997
Last Updated: 2022-03-15
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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COMPLETED
171 participants
OBSERVATIONAL
2019-09-01
2020-06-30
Brief Summary
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The purpose of our study is to evaluate the accuracy and inter-reader reproducibility of the PI-RADS v2.1 score on a large set of 171 prostate MRIs using 21 readers of varying experience.
Twenty-one readers (14 seniors and 7 juniors) from 9 different institutions and with varying experience in prostate mpMRI accepted to participate to the study.
Reader will assess the dataset independently and will be blinded to the other readers' results. They also be blinded to clinical and biochemical data.
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Detailed Description
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Conditions
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Study Design
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COHORT
RETROSPECTIVE
Study Groups
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171 mpMRIs corresponding to consecutive patients who underwent
The mpMRIs were performed on a 1.5T GE MR unit or on a 3T GE or Philips MR units. All mpMRIs included T2-weighted imaging, diffusion-weighted imaging (maximal b value: 2000 s/mm²) and dynamic contrast-enhanced imaging.
Assessment of the accuracy of the PI-RADS v2.1 score for predicting the presence of ISUP ≥2 prostate cancer at subsequent biopsy in the dataset of the 171 MRIs for 21 different readers.
1. Ass of targeted suspect lesions
On each mpMRI,radiologist will contour lesions that were targeted at subsequent biopsy based on reports. Contours will be disclosed to readers who will assess,for each lesion:
* Likert score("gut feeling"ie subjective ass of the likelihood that lesion is clinically significant prostate cancer(5-level scale))
* PI-RADSv2, PI-RADSv2.1 score(by strictly applying the published PI-RADS criteria)
* EPE score(ie the likelihood of extraprostatic extension;5-level subjective scale without predefined criteria)
* Max diameter
2. Def of add suspect lesions Readers could define suspect"additional targets"(AT);for each AT,they will provide the same criteria. It is expected that, for these suspect AT,at least one score is≥3
3. Ass of lobes Scores of prostate lobes will be automatically calculated based on 2 previous steps of reading. However,in lobes with no suspect lesion,readers could define whether same criteria are1or2,in peripheral zone and transition zone
Interventions
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Assessment of the accuracy of the PI-RADS v2.1 score for predicting the presence of ISUP ≥2 prostate cancer at subsequent biopsy in the dataset of the 171 MRIs for 21 different readers.
1. Ass of targeted suspect lesions
On each mpMRI,radiologist will contour lesions that were targeted at subsequent biopsy based on reports. Contours will be disclosed to readers who will assess,for each lesion:
* Likert score("gut feeling"ie subjective ass of the likelihood that lesion is clinically significant prostate cancer(5-level scale))
* PI-RADSv2, PI-RADSv2.1 score(by strictly applying the published PI-RADS criteria)
* EPE score(ie the likelihood of extraprostatic extension;5-level subjective scale without predefined criteria)
* Max diameter
2. Def of add suspect lesions Readers could define suspect"additional targets"(AT);for each AT,they will provide the same criteria. It is expected that, for these suspect AT,at least one score is≥3
3. Ass of lobes Scores of prostate lobes will be automatically calculated based on 2 previous steps of reading. However,in lobes with no suspect lesion,readers could define whether same criteria are1or2,in peripheral zone and transition zone
Eligibility Criteria
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Inclusion Criteria
* Performed between September 2015 and July 2016
* No history of prostate cancer at the time of the mpMRI
Exclusion Criteria
* Patients under Active Surveillance
MALE
No
Sponsors
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Hospices Civils de Lyon
OTHER
Responsible Party
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Locations
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Hôpital Edouard Herriot
Lyon, , France
Countries
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Other Identifiers
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MULTI_2020
Identifier Type: -
Identifier Source: org_study_id
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