Use of Artificial Intelligence in the Symptomatic BReAst Clinic SEtting
NCT ID: NCT06578988
Last Updated: 2024-08-30
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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ACTIVE_NOT_RECRUITING
25000 participants
OBSERVATIONAL
2024-03-01
2025-10-01
Brief Summary
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It is reasonable to think that these systems could be useful in the context of symptomatic breast clinic. However, these systems developed in the screening setting have unknown performance in the context of symptomatic breast clinic.
It is therefore important to test the performance of these systems in this alternative context.
This study will use retrospective data, from where it is possible to determine ground truth outcomes with greater confidence, accessing relatively large volumes of data with less patient burden when compared to prospective studies. This important cohort of patients has been less investigated to date, mainly because symptomatic data is typically more difficult to curate than screening data where key data is methodically prospectively collected.
The proposed work will be carried out in collaboration with a selected AI vendor and local clinical teams to define optimal use case scenarios for the symptomatic breast clinic.
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Detailed Description
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Ultrasound and / or mammography are typically performed and reported by the imaging team at the same visit, with biopsy performed when indicated. This service is an important part of cancer care provision, with approximately half of the breast cancers diagnosed presenting via the symptomatic service rather than identified at screening.
It is important to note that cancers diagnosed symptomatically tend to be larger and more aggressive with worse outcome than those diagnosed via screening. The volume of referrals to the National Health Service (NHS) symptomatic service has risen over the last decade, placing increased pressure on service delivery, in breast imaging.
Artificial Intelligence (AI) systems for the classification of mammography images have been developed and are beginning to be trialled and deployed in a breast cancer screening setting with encouraging results. It is reasonable to think that these systems could be useful in the context of symptomatic breast clinic. However, these systems developed in the screening setting have unknown performance in the context of symptomatic breast clinic. It is therefore important to test the performance of these systems in this alternative context.
Conditions
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Study Design
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CASE_ONLY
RETROSPECTIVE
Study Groups
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Symptomatic breast clinic.
Patients 18 years or older attending symptomatic breast clinic from January 2015 to December 2019.
Mammography Images
Ultrasound and / or mammography are typically performed and reported by the imaging team at the same visit, with biopsy performed when indicated. This service is an important part of cancer care provision, with approximately half of the breast cancers diagnosed presenting via the symptomatic service rather than identified at screening.
Interventions
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Mammography Images
Ultrasound and / or mammography are typically performed and reported by the imaging team at the same visit, with biopsy performed when indicated. This service is an important part of cancer care provision, with approximately half of the breast cancers diagnosed presenting via the symptomatic service rather than identified at screening.
Eligibility Criteria
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Inclusion Criteria
* Mammography images, including both full field two-dimensional digital mammography and digital breast tomosynthesis.
* Dates of attendance will be from January 2015\* to December 2019 at the lead data collection site. Dates of collection may be different at the other sites depending on local data curation consideration but will be a minimum of 2 years prior to study start to allow determination of ground truth.
* If any mammography images prior to 2015 should be available at the lead site, these will be collected as well (a maximum of 3). Prior mammograms will also be collected at the other sites if available, depending on local PACS set-up.
Exclusion Criteria
* Patients on the National data opt out.
18 Years
ALL
No
Sponsors
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Imperial College Healthcare NHS Trust
OTHER
St George's University Hospitals NHS Foundation Trust
OTHER
Royal Surrey County Hospital NHS Foundation Trust
OTHER
Royal Marsden NHS Foundation Trust
OTHER
Responsible Party
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Locations
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The Royal Marsden NHS Foundation Trust
Sutton, Surrey, United Kingdom
Countries
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Other Identifiers
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CCR5910
Identifier Type: -
Identifier Source: org_study_id
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