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Figure 1 from Development and Validation of a Multimodal–Multitask Deep Learning Approach for Estimating Late Distant Recurrence Risk in HR-Positive Early Breast Cancer

Year: 2026
Type: other
Abstract: A, Overview of the M3T model workflow. The model was developed using the NSABP B-42 translational cohort (N = 2,271) with five-fold cross-validation, integrating H&E image–derived features and selected tabular clinicopathologic features through the M3T (multimodal, multitask transformer). An auxiliary task predicting the lowest BMD T-score enhanced prognostic performance and improved stratification of patients with differential ELT benefit but was not required for model inference. The model outputs a continuous risk score that is dichotomized into low- and high-risk groups. Independent external validation was performed in the TAILORx translational cohort (N = 4,300). Prognostic, predictive, and calibration analyses were conducted to evaluate model performance. B, End-to-end image preprocessing, feature extraction, model training, and output architecture. Tissue regions were detected from H&E-stained WSIs, tiled at 10× magnification, and processed using CTransPath to generate tile-level image embeddings. Tile-level image embeddings and clinicopathologic features were projected into a shared representation space and processed through transformer encoder and decoder modules. During training, an auxiliary task predicting the lowest BMD T-score was incorporated to improve prognostic performance and stratification of patients with differential ELT benefit. The primary task generated a continuous risk score for late DR risk stratification. The dashed box shows the detailed architecture of the transformer encoder (left) and transformer decoder (right).
Open Access status: gold
OpenAlex ID: W7171950350
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