Advancing Neoadjuvant Chemotherapy Response Prediction through Deep Learning-Enabled Retrospective Quanfication of Pharmacokinetics
Motivation: While multiphasic contrast-enhanced MRI has propelled noninvasive pCR prediction in breast cancer, its limited temporal resolution restricts quantitative analysis, affecting generalizability and interpretability. Goal(s): To enhance pCR prediction, we integrated retrospective pharmacokinetic quantification by addressing the temporal resolution limit using deep learning. Approach: We incorporated a novel retrospective pharmacokinetic quantification approach into our pCR prediction model to better capture the tumor microenvironment's pharmacokinetic indicators. Results: Our approach improved predictive accuracy in external test datasets, demonstrating the method's superior performance and broader applicability. Impact: Deep-learning pharmacokinetic quantification enhances the accuracy and applicability of pCR prediction using multiphasic DCE-MRI, offering the potential for precise pre-treatment evaluation that could streamline NAC targeting and minimize initiation delays for breast cancer patients unlikely to respond to standard treatments.
Authors
- Yibin Xie (ORCID: https://orcid.org/0000-0002-0333-567X)
- Stephen J. Pandol (ORCID: https://orcid.org/0000-0003-0818-6017)
- Chaowei Wu (ORCID: https://orcid.org/0000-0002-1060-9149)
- Nan Wang (ORCID: https://orcid.org/0000-0002-7616-8083)
- Lixia Wang (ORCID: https://orcid.org/0000-0002-2304-7536)
- Debiao Li (ORCID: https://orcid.org/0000-0001-8560-8231)
- Anthony Christodoulou (ORCID: https://orcid.org/0000-0002-9334-8684)
Publication Details
- Journal
- Proceedings on CD-ROM - International Society for Magnetic Resonance in Medicine. Scientific Meeting and Exhibition/Proceedings of the International Society for Magnetic Resonance in Medicine, Scientific Meeting and Exhibition
- Published
- 2024-11-26
- DOI
- https://doi.org/10.58530/2024/2117
- Primary Topic
- Computational Drug Discovery Methods
- Type
- article
- Field-Weighted Citation Impact
- 0.00