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Multimodal prediction for radiotherapy-induced hematologic toxicity in rectal cancer patients

AI Summary
  • Transformer-based multimodal fusion model integrating CT, dose maps, biomarkers and demographics predicted radiotherapy-induced hematologic toxicity with AUCs 0.828 internal, 0.757 and 0.756 external.
  • Initial hematologic biomarkers were the strongest unimodal predictor; planning target volume was the most sensitive anatomical region.
  • The model demonstrated interpretability and generalisation, offering actionable insights to personalise radiotherapy planning for high-risk locally advanced rectal cancer patients.
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NPJ Precis Oncol. 2026 May 14. doi: 10.1038/s41698-026-01476-0. Online ahead of print.

ABSTRACT

Early identification of acute hematologic toxicity (HT) in locally advanced rectal cancer (LARC) patients undergoing radiotherapy is crucial for optimizing clinical outcomes. Here, we retrospectively collected multi-center LARC patients (n = 464, n = 56, and n = 79) with complete CT images, dose maps, hematologic biomarkers, and demographic information. A Transformer-based multimodal fusion model was constructed to combine the visual and non-visual representation features for HT prediction, and the study also testified to the modality-specific and region-specific contributions to HT. The multimodal fusion model achieved a state-of-the-art HT prediction performance in LARC patients: with an area under the curve (AUC) of 0.828 (95% confidence interval [CI]: 0.820-0.835), 0.757 (95% CI: 0.750-0.766), and 0.756 (95% CI: 0.752-0.762) in internal and two external testing datasets. The initial hematologic biomarkers were the best unimodal risk indicator, while the planning target volume served as the most sensitive region. The study confirms the sole and combined contributions of each modality to the radiotherapy-induced HT in LARC patients, and the multimodal fusion model shows promising interpretability and generalization for HT occurrence, which offers valuable insights to optimize personalized treatment plans for high-risk patients.

PMID:42135422 | DOI:10.1038/s41698-026-01476-0

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