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In situtumor model for longitudinal in silico imaging trials
Aunnasha Sengupta1, Miguel A Lago1, Aldo Badano1
1Division of Imaging, Diagnostics, and Software Reliability, Office of Science and Engineering Laboratories, Center for Devices and Radiological Health, U.S. Food and Drug Administration, Silver Spring, MD 2099, United States of America.
This study introduces a computational model simulating breast cancer lesion growth, considering tissue stiffness. The model shows how cancer cells navigate differing tissue rigidities, aiding in virtual trials for breast cancer progression.
Area of Science:
- Computational modeling
- Medical imaging
- Biophysics
Background:
- Breast cancer progression is influenced by the mechanical properties of surrounding tissues.
- Understanding how tumor cells interact with varying tissue elasticity is crucial for accurate modeling.
Purpose of the Study:
- To develop a computational model simulating breast cancer lesion growth based on anatomical structure stiffness.
- To investigate how differential tissue resistance affects tumor morphology.
- To generate realistic digital mammogram (DM) images of simulated lesions for validation.
Main Methods:
- Utilized a computational model incorporating tissue elasticity (ligaments as rigid, fat/glandular tissue as soft).
- Simulated lesion growth within fatty breast models from the Virtual Imaging Clinical Trials for Regulatory Evaluation (VICTRE) pipeline.
- Generated digital mammograms using a simulated mammography system (Siemens Mammomat Inspiration) for visualization and validation.
- Conducted a reader study comparing simulated lesions with real mammograms from the DDSM dataset.
Main Results:
- The model demonstrated that simulated cancer cells preferentially grow in softer tissues, circumventing stiffer structures like ligaments.
- Digital mammogram images effectively illustrated lesion integration with anatomical backgrounds.
- Reader study indicated the simulated lesions' realism when compared to real mammograms.
- Average simulation time was approximately 2.5 hours, varying with the local environment.
Conclusions:
- The developed lesion growth model accurately simulates breast cancer progression influenced by anatomical topography.
- This model enhances the capability for longitudinal in silico trials in breast cancer research.
- The findings support the use of computational models for understanding tumor behavior in diverse tissue environments.
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