Aug 2026· Proceedings of the 32nd ACM SIGKDD Conference on Knowledge Discovery and Data Mining V.2· 0 citations· 28 references
TL;DR
Empirical evaluation and robustness experiments show that M2DDI maintains high predictive accuracy even when modality-specific information is partially missing, outperforming existing methods under similar conditions and establish M2DDI as an effective and mechanism-aware solution for comprehensive DDI prediction.
Abstract
Drug-drug interaction (DDI) event prediction is critical for ensuring patient safety and optimizing therapeutic outcomes. Existing computational approaches are limited by their inability to jointly model the heterogeneous mechanisms underlying DDIs, which span molecular structure, pharmacodynamic function, and network-mediated relations. To address this limitation, we introduce M2DDI, a unified framework for dynamic multimodal fusion in DDI prediction. M2DDI utilizes a Mixture-of-Experts architecture, with each expert dedicated to a distinct pharmacological modality. A novel prior-enhanced dual-path gating strategy adaptively selects relevant experts for each drug pair by integrating mechanism-matched feature queries and ATC-based biomedical priors, thereby aligning expert selection with underlying pharmacological mechanisms and addressing the challenge of data incompleteness. Empirical evaluation on benchmark datasets demonstrates that M2DDI achieves state-of-the-art performance, particularly in new drug scenarios. Additional robustness experiments show that M2DDI maintains high predictive accuracy even when modality-specific information is partially missing, outperforming existing methods under similar conditions. Analysis of expert selection patterns further confirms alignment with established pharmacological mechanisms. These results establish M2DDI as an effective and mechanism-aware solution for comprehensive DDI prediction. The code is available at: https://github.com/RunqingXuCn/M2DDI.
This review provides a unified roadmap to accelerate the clinical deployment of multimodal drug response prediction and proposes five actionable directions, namely privacy-preserving benchmarks, causally interpretable models, temporal dynamic frameworks, cross-domain generalization, and lightweight clinical tools.
Jing-Wen Fang, Zihan Wang, Jun-Hao Shao et al.· Drug Discoveries & Therapeut...· 0 citations
MKASynergy, an adaptive drug synergy prediction method based on a mixture-of-experts kernel mechanism, achieves competitive predictive performance and visualization analysis confirms the model’s effectiveness in feature decoupling and helps interpret latent drug synergistic mechanisms.
Cundong Lin, Jiancheng Ni, Ying Yang et al.· Network Modeling Analysis in...· 0 citations
Experiments demonstrate that HSAF-DDI achieves superior overall performance compared to state-of-the-art methods, indicating the critical role of fine-grained biological features in improving the DDI prediction performance.
Xiaoli Lin, Si-Yuan Zhang, Bo Li et al.· Journal of Chemical Informat...· 0 citations
EQTri-DTI is designed to integrate three modality-specific networks to encode 1D protein sequences, 2D molecular images, and 3D drug structures and develops a joint uncertainty quantification scheme by calculating the weight summation of evidential uncertainty and prediction entropy from the aforementioned output, enabling a more comprehensive and nuanced assessment of uncertainties.
T-DDI pairs confidence-stratified predictions with LIME-based feature-level explanations and a web application for screening, supporting more reliable drug safety monitoring, and outperforming all evaluated baselines within the architectures and datasets considered here.
Q. Kha, Duc-Quang-Anh Nguyen, Phi Pham Van Hoang et al.· npj Digital Medicine· 0 citations
KGDDA is proposed, a multimodal framework designed for drug-disease association prediction that synergistically integrates KGs with medical ontologies, enabling the adaptive capture of intricate drug-disease interactions.
Qichang Zhao, Qiao Ling, Muhammad Habibulla Alamin et al.· IEEE transactions on computa...· 0 citations
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