SHIFT-DRP: Dynamic Multi-Scale Active Learning for Drug Response Prediction
Xintao Wang1, Huiyan Xu1, Yanpeng Zhao1
1School of Mechatronic Engineering and Automation, Shanghai University, Shanghai 200444, China.
Abstract:
Deep learning models show promise for drug response prediction in personalized cancer treatment, but exhibit limited prediction capability for novel drug-cell line combinations due to insufficient coverage of the chemical spaces in training data. The vast combinatorial space of drug-cell line pairs makes comprehensive experimental screening impractical, while uniform sampling is inefficient, as a large proportion of randomly selected experiments contain redundant information. To address this challenge, we present SHIFT-DRP, an active learning framework that intelligently selects drug-cell line pairs for experimental validation to maximize model improvement under limited resources. The core approach is a dynamic sampling strategy that transitions from diversity-focused exploration to uncertainty-driven refinement, ensuring both broad feature space coverage and targeted improvement where the model lacks adequate learning. The framework employs a pretrained model for molecular representation and a cross-attention mechanism to model drug-cell line interactions. Evaluation on four data sets demonstrates SHIFT-DRP's superiority over existing active learning methods, achieving better prediction performance while reducing the required experimental resources by 24% compared with uniform sampling. Ablation studies confirm the effectiveness of the dynamic sampling strategy, and case studies reveal SHIFT-DRP's ability to identify structurally similar compounds that exhibit divergent responses in the same cell line. SHIFT-DRP offers an efficient solution for guided experimental screening and data collection in drug response prediction with significant implications for precision medicine development.
More Related Videos
09:41An Organotypic High Throughput System for Characterization of Drug Sensitivity of Primary Multiple Myeloma Cells
Published on: July 15, 2015
08:49Incorporating Target Protein Structure Flexibility and Dynamics in Computational Drug Discovery Using Ensemble-Based Docking Analysis
Published on: June 20, 2025
Related Concept Videos
Drug Discovery: Overview
Structure-Activity Relationships and Drug Design
SAR studies the intricate relationship between a drug's chemical structure and biological activity. It focuses on understanding how modifications to a drug's structure can influence...
Dose-Response Relationship: Overview
Factors Affecting Drug Response: Overview
Analysis of Population Pharmacokinetic Data
Model Approaches for Pharmacokinetic Data: Distributed Parameter Models
The distributed parameter models are specifically designed to account for variations and differences in some drug classes. This model is particularly useful for assessing regional concentrations of anticancer or...
