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Related Experiment Video

Updated: May 24, 2026

A Multimodal Imaging Framework to Advance Phenotyping of Living Label-free Breast Cancer Cells
10:37

A Multimodal Imaging Framework to Advance Phenotyping of Living Label-free Breast Cancer Cells

Published on: August 22, 2025

A Digital Twin-Inspired Closed-Loop Latent Simulation Framework for Cross-Cohort Breast Cancer Subtype Classification

Nabil Hezil, Ahmed Bouridane, Rifat Hamoudi

    IEEE Journal of Biomedical and Health Informatics
    |May 22, 2026
    PubMed
    Summary
    This summary is machine-generated.

    This study introduces a novel deep learning framework for breast cancer subtype classification, improving accuracy by refining patient representations iteratively. The Cross-Cohort Modality-Disjoint Latent Simulation (CDLS) framework enhances subtype prediction using diverse data types.

    Related Experiment Videos

    Last Updated: May 24, 2026

    A Multimodal Imaging Framework to Advance Phenotyping of Living Label-free Breast Cancer Cells
    10:37

    A Multimodal Imaging Framework to Advance Phenotyping of Living Label-free Breast Cancer Cells

    Published on: August 22, 2025

    Area of Science:

    • Computational Biology and Bioinformatics
    • Machine Learning in Oncology
    • Medical Image Analysis

    Background:

    • Current deep learning models for breast cancer PAM50 subtype classification use a single-pass prediction, limiting iterative refinement and uncertainty analysis.
    • Integrating diverse data modalities like histopathology, transcriptomics, and mammography presents challenges due to missing data across cohorts.
    • Existing methods often rely on per-patient data fusion, which is not feasible when patients lack complete multimodal data.

    Purpose of the Study:

    • To develop an advanced deep learning framework, the Cross-Cohort Modality-Disjoint Latent Simulation (CDLS), for improved breast cancer subtype classification.
    • To enable iterative representation refinement and uncertainty trajectory analysis within a closed-loop system.
    • To effectively integrate heterogeneous data from multiple cohorts under a modality-disjoint regime.

    Main Methods:

    • Implemented a Cross-Cohort Modality-Disjoint Latent Simulation (CDLS) framework integrating histopathology (WSI), transcriptomics (RNA-seq), mammography, and clinical data.
    • Employed a Proximal Policy Optimization (PPO)-governed stochastic policy to refine a 7-dimensional latent state ($z$) over 5 optimization steps using a Twin-GRU transition model.
    • Incorporated a closed-loop latent feedback mechanism involving k-Nearest Neighbors (kNN) retrieval for aligning simulated states with real patient embeddings.

    Main Results:

    • Achieved a Balanced Accuracy of 0.870 ± 0.044 and MCC of 0.904 ± 0.046 in multi-seed evaluations (n=4).
    • Cross-validation confirmed stability with Accuracy 0.871 ± 0.029 and MCC 0.897 ± 0.038.
    • The chosen 7-dimensional latent space bottleneck was guided by intrinsic dimensionality estimates (d_id = 6.3 ± 0.4).

    Conclusions:

    • The CDLS framework offers a robust approach for breast cancer subtype classification by enabling iterative representation refinement and handling modality-disjoint data.
    • The closed-loop latent feedback mechanism effectively aligns simulated and real patient representations, enhancing classification performance.
    • PPO selection was based on trajectory geometry properties, ensuring broader latent coverage and path diversity, crucial for complex biological systems.