Real-world risk-assessment using the Mirai breast cancer risk prediction model: A preliminary analysis of patients from a comprehensive cancer screening clinic.

S Sriya Yalamanchili (Inova Health System, Fairfax, VA) M Madeline Kaltman (University of Wisconsin, Madison, WI) R Raissa Kentsa (2National Cancer Institute, NIH, Bethesda, United States) R Reema Patel (University of Pittsburgh, Pittsburgh, PA) J John F. Deeken (Inova Schar Cancer Institute, Fairfax, VA) S Sanja Karovic (Inova Schar Cancer Institute, Fairfax, VA) E Erik Dvergsten (Inova Schar Cancer Institute, Fairfax, VA) B Bryan Bassig (Inova Health System, Fairfax, VA) R Rebecca Davidson Kaltman (Saville Cancer Screening and Prevention Center, Inova Schar Cancer Institute, Fairfax, VA)

Abstract

e22560 Background: The current standard of care for breast cancer risk assessments is the Tyrer-Cuzick (TC) model, which requires clinical variables including family history, hormone exposure and breast density. Mirai, a validated artificial intelligence program designed to determine breast cancer risk based solely on mammographic images, requires less clinical data and predicts the probability that a woman will develop breast cancer over the next five years. Our study aims to describe Mirai performance on mammograms from a sample of women that were seen for a breast cancer risk assessment in a comprehensive cancer screening clinic within a large health system. Methods: This preliminary descriptive analysis includes 84 identified women with mammograms available for Mirai analysis and an available TC lifetime risk estimate of developing breast cancer. All patients were seen between 12/2021 and 6/2023. Women with known pathogenic variants or hereditary cancer syndromes and those with prior breast cancer diagnoses, including DCIS, were excluded. Probabilities from the Mirai model were categorized as low risk ( < 1.8%), and then intermediate or high-risk based on the median cut-point of probabilities > 1.8%. TC lifetime risk estimates were categorized as low ( < 20%), intermediate (20% - < 40%), or high ( > 40%). Mirai results were compared to TC model results and the percentage of patients who would have a change in risk level based on using Mirai instead of TC was assessed. Results: Patients had an average age of 47 years (range: 29-72 years) and 64% were White, 13% were Asian, 7% were Black/African-American, and 15% were of unknown or another race. Lifetime breast cancer risk estimated from the TC model ranged from 6.4%-56.0% with 19.0% of patients categorized as low-risk (n = 16), 71.4% as intermediate risk (n = 60), and 9.5% as high-risk (n = 8). Comparatively, 5-year risk prediction estimates from Mirai ranged from 0.97%-5.3% with 67.9% (n = 57), 17.9% (n = 15), and 14.3% (n = 12) categorized as low, intermediate, and high-risk, respectively. Overall, 29.8% of patients (n = 25) were concordant in the assigned risk category from the TC and Mirai models. Of the 59 (70.2%) patients that had a discordant risk assessment category, 47 (79.7%) were found to be at a lower risk by the Mirai model compared to their TC score. Twelve (20.3%) patients undergoing Mirai had a higher risk compared to their TC score. Conclusions: These preliminary results from patients seen for a breast cancer risk assessment suggest an overall modest concordance in assigned risk assessment categories. The Mirai model demonstrates its potential in deescalating short-term breast cancer screening in a majority of patients seen in a high-risk clinic by using a shorter-interval, more accurate risk estimate that does not rely on historical data. Larger trials are needed to prospectively validate these findings.

Article Details

Volume / Issue Vol. 44, Issue 16_suppl
Published June 01, 2026
ISSN 0732-183X
Publisher Lippincott Williams & Wilkins

Journal Info

Journal of Clinical Oncology

Lippincott Williams & Wilkins

ISSN: 0732-183X Health Sciences

Authors (9)

S

Sriya Yalamanchili

Inova Health System, Fairfax, VA

M

Madeline Kaltman

University of Wisconsin, Madison, WI

R

Raissa Kentsa

2National Cancer Institute, NIH, Bethesda, United States

R

Reema Patel

University of Pittsburgh, Pittsburgh, PA

J

John F. Deeken

Inova Schar Cancer Institute, Fairfax, VA

S

Sanja Karovic

Inova Schar Cancer Institute, Fairfax, VA

E

Erik Dvergsten

Inova Schar Cancer Institute, Fairfax, VA

B

Bryan Bassig

Inova Health System, Fairfax, VA

R

Rebecca Davidson Kaltman

Saville Cancer Screening and Prevention Center, Inova Schar Cancer Institute, Fairfax, VA