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An Enhanced Artificial Intelligence Breast MRI Interpretation System (IntelliScan)

J

Jamil Kanfoud

Status

Unknown

Conditions

Breast Cancer

Treatments

Diagnostic Test: Breast MRI interpretation

Study type

Interventional

Funder types

Other

Identifiers

Details and patient eligibility

About

Interpretation of breast MR images is a very time-consuming process and places a great burden on breast radiologists. This project aims to develop a technical solution that addresses this healthcare challenge by developing a system that is able to automatically interpret breast MR images in order to aid the radiologist in their diagnosis.

Full description

Breast cancer is the most common type of cancer in women worldwide, with nearly 1.7 million new cases diagnosed in 2015. In the UK, one in five cases of breast cancer results in a fatality. The IntelliScan project aims to develop a technological solution that addresses a significant healthcare challenge. IntelliScan will develop a software system that will be able to interpret breast MR images automatically in order to identify potential breast cancers.

Regular MRI screening of the breast is offered to women from the age of 20, who are at higher risk of developing breast cancer. MR image sequences provide a large amount of information to the radiologist and the interpretation of images is a manual process, which is very time consuming. The high number of women eligible for MRI screening combined with the amount of data provided by MRI scans places a great burden on healthcare systems. Therefore, automatisation of this process would greatly relieve this burden and also has the potential to provide more accurate diagnoses.

In this first study, the system's user interface as well as the algorithm will be developed using existing MRI scans. Existing MRI scans with known breast anomalies will be used to develop the decision-making basis for the algorithm. The system will then be tested using existing MRI scans without information about possible anomalies and results will be compared to results from the software system currently in use. In addition, the user-friendliness of the system's user interface will also be evaluated.

Enrollment

1,526 estimated patients

Sex

Female

Ages

20+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Breast MRI scans
  • MRI examinations undertaken at partner NHS Trust in the UK
  • MRI examinations undertaken on the MRI system currently installed at partner NHS Trust site (since 2008)

Exclusion criteria

  • Incomplete breast MRI datasets
  • Breast MRI without lesions
  • Breast lesion on MRI not biopsied

Trial design

Primary purpose

Diagnostic

Allocation

N/A

Interventional model

Single Group Assignment

Masking

Single Blind

Trial contacts and locations

0

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Central trial contact

Jamil Kanfoud, M.Eng.; Susann Wolfram, PhD

Data sourced from clinicaltrials.gov

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