Back to all papers

Incorporating global-local tissue changes to predict future breast cancer from longitudinal screening mammograms.

February 16, 2026pubmed logopapers

Authors

Wang X,Tan T,Gao Y,Marcus E,Zhou HY,Lu C,Han L,Portaluri A,Su R,Zhang T,Liang X,Beets-Tan R,Pinker K,Sun Y,Mann R,Teuwen J

Affiliations (14)

  • Department of Radiology, Netherlands Cancer Institute (NKI), Amsterdam, 1066 CX, The Netherlands; GROW School for Oncology and Development Biology, Maastricht University, Maastricht, 6200 MD, The Netherlands; AI for Oncology, Netherlands Cancer Institute (NKI), Amsterdam, 1066 CX, The Netherlands.
  • Faculty of Applied Sciences, Macao Polytechnic University, Macao, 999078, China. Electronic address: [email protected].
  • Department of Radiology, Netherlands Cancer Institute (NKI), Amsterdam, 1066 CX, The Netherlands; GROW School for Oncology and Development Biology, Maastricht University, Maastricht, 6200 MD, The Netherlands; Department of Radiology, University Medical Center Utrecht, Utrecht University, Utrecht, 3584 CX, The Netherlands.
  • AI for Oncology, Netherlands Cancer Institute (NKI), Amsterdam, 1066 CX, The Netherlands.
  • School of Biomedical Engineering, Tsinghua University, Beijing, 100084, China.
  • Department of Radiology, Netherlands Cancer Institute (NKI), Amsterdam, 1066 CX, The Netherlands; Department of Medical Imaging, Radboud University Medical Centre, Nijmegen, 6525 GA, The Netherlands.
  • Department of Radiology, Netherlands Cancer Institute (NKI), Amsterdam, 1066 CX, The Netherlands; Department of Medical Imaging, Radboud University Medical Centre, Nijmegen, 6525 GA, The Netherlands; Department of Biomedical Sciences and Morphologic and Functional Imaging, AOU G. Martino, University of Messina, Messina, 98100, Italy.
  • Department of Electrical Engineering, Eindhoven University of Technology, Eindhoven, 5612WH, The Netherlands.
  • Department of Radiology, Netherlands Cancer Institute (NKI), Amsterdam, 1066 CX, The Netherlands; GROW School for Oncology and Development Biology, Maastricht University, Maastricht, 6200 MD, The Netherlands; Department of Medical Imaging, Radboud University Medical Centre, Nijmegen, 6525 GA, The Netherlands.
  • Department of Radiology, Netherlands Cancer Institute (NKI), Amsterdam, 1066 CX, The Netherlands; GROW School for Oncology and Development Biology, Maastricht University, Maastricht, 6200 MD, The Netherlands.
  • Department of Radiology, Columbia University Irving Medical Center, New York, NY 10032, USA.
  • Faculty of Applied Sciences, Macao Polytechnic University, Macao, 999078, China; Department of Electrical Engineering, Eindhoven University of Technology, Eindhoven, 5612WH, The Netherlands.
  • Department of Radiology, Netherlands Cancer Institute (NKI), Amsterdam, 1066 CX, The Netherlands; Department of Medical Imaging, Radboud University Medical Centre, Nijmegen, 6525 GA, The Netherlands. Electronic address: [email protected].
  • AI for Oncology, Netherlands Cancer Institute (NKI), Amsterdam, 1066 CX, The Netherlands; Department of Medical Imaging, Radboud University Medical Centre, Nijmegen, 6525 GA, The Netherlands. Electronic address: [email protected].

Abstract

Early detection of breast cancer (BC) through mammography screening is critical for reducing mortality and improving patient outcomes. However, full-population-based, age-driven screening might not lead to optimal resource use and may enlarge screening associated harms in low risk women. Accurate and interpretable BC risk prediction is essential to improve strategies and make screening more personalized. Although recent deep learning models have shown promise in leveraging mammograms for risk stratification, challenges remain in interpretable modeling of temporal changes, efficiently capturing multi-scale risk tissue features from large-scale images, and precise time prediction to enhance clinical interpretability. In this study, we propose Tarcking-Aware Breast Cancer Risk model (TA-BreaCR), a novel framework that integrates local-to-global multiscale longitudinal tissue changes and explicitly models the ordinal relationship of time to BC events, enabling joint prediction of both future BC risk and estimated time to onset. The model is evaluated on two datasets (In-house and EMBED), outperforming existing and state-of-the-art methods in both risk classification and time-to-event prediction tasks. Visualization analysis reveals consistent attention to high-risk regions over time, enhancing interpretability. These results highlight the potential of TA-BreaCR to support individualized BC screening and prevention.

Topics

Breast NeoplasmsMammographyEarly Detection of CancerRadiographic Image Interpretation, Computer-AssistedJournal Article

Ready to Sharpen Your Edge?

Subscribe to join 11k+ peers who rely on RadAI Slice. Get the essential weekly briefing that empowers you to navigate the future of radiology.

We respect your privacy. Unsubscribe at any time.