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Artificial intelligence for breast cancer detection in screening mammography in Sweden: a prospective, population-based, paired-reader, non-inferiority study

Karin Dembrower, MD et al. - The LANCET Digital Health 2023

AUTHORS

Karin Dembrower, MD

Alessio Crippa, PhD

Eugenia Colón, MD

Prof Martin Eklund, PhD

Fredrik Strand, MD

and theScreenTrustCAD Trial Consortium

Trial Consortium Members

Karin Dembrower, Capio S:t Göran Hospital and Karolinska Institutet

Alessio Crippa, Karolinska Institutet

Eugenia Colón, Capio S:t Göran Hospital

Martin Eklund, Karolinska Institutet

Fredrik Strand, Karolinska University Hospital and Karolinska Institutet

Anders Byström, Capio S:t Göran Hospital

Jonathan Waldenström, Capio S:t Göran Hospital

Lennart Skärblom, Capio S:t Göran Hospital

Astrid Rocchi, Capio S:t Göran Hospital

Kjell Hågemo, Capio S:t Göran Hospital Karin Torneman, Capio S:t Göran Hospital

Ingrid Wiklander-Bråkenhielm, Capio S:t Göran Hospital

Johanna Swärd, Capio S:t Göran Hospital

Maria Balarova, Capio S:t Göran Hospital

Anca Plotoaga, Capio S:t Göran Hospital

Edith Herterich Capio S:t göran Hospital

PUBLISHED

The LANCET Digital Health 2023

Summary


Background

Artificial intelligence (AI) as an independent reader of screening mammograms has shown promise, but there are few prospective studies. Our aim was to conduct a prospective clinical trial to examine how AI affects cancer detection and false positive findings in a real-world setting.


Methods

ScreenTrustCAD was a prospective, population-based, paired-reader, non-inferiority study done at the Capio Sankt Göran Hospital in Stockholm, Sweden. Consecutive women without breast implants aged 40–74 years participating in population-based screening in the geographical uptake area of the study hospital were included. The primary outcome was screen-detected breast cancer within 3 months of mammography, and the primary analysis was to assess non-inferiority (non-inferiority margin of 0·15 relative reduction in breast cancer diagnoses) of double reading by one radiologist plus AI compared with standard-of-care double reading by two radiologists. We also assessed single reading by AI alone and triple reading by two radiologists plus AI compared with standard-of-care double reading by two radiologists. This study is registered with ClinicalTrials.gov, NCT04778670.

Findings

From April 1, 2021, to June 9, 2022, 58 344 women aged 40–74 years underwent regular mammography screening, of whom 55 581 were included in the study. 269 (0·5%) women were diagnosed with screen-detected breast cancer based on an initial positive read: double reading by one radiologist plus AI was non-inferior for cancer detection compared with double reading by two radiologists (261 [0·5%] vs 250 [0·4%] detected cases; relative proportion 1·04 [95% CI 1·00–1·09]). Single reading by AI (246 [0·4%] vs 250 [0·4%] detected cases; relative proportion 0·98 [0·93–1·04]) and triple reading by two radiologists plus AI (269 [0·5%] vs 250 [0·4%] detected cases; relative proportion 1·08 [1·04–1·11]) were also non-inferior to double reading by two radiologists.


Interpretation

Replacing one radiologist with AI for independent reading of screening mammograms resulted in a 4% higher non-inferior cancer detection rate compared with radiologist double reading. Our study suggests that AI in the study setting has potential for controlled implementation, which would include risk management and real-world follow-up of performance.


Funding

Swedish Research Council, Swedish Cancer Society, Region Stockholm, and Lunit.

Read the full paper
AIBreastBreast CancerCancer AIComputer VisiondiagnosticDiagnosticsEuropeImagingLunitLunit INSIGHTmammographyRadiologyResearchscreeningThe LANCET

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