Abstract
Dynamic contrast-enhanced MRI (DCE-MRI) images are increasingly used for assessing cancer treatment outcome. These time sequences are typically affected by motion, which causes significant errors in tracer kinetic model analysis. Current intra-sequence registration methods for contrast enhanced data either assume restricted transformations (e.g. translation) or employ continuous optimization, which is prone to local optima. In this work, we propose a new approach to DCE-MRI intra-sequence registration and pharmacokinetic modelling, which is formulated in an MRF optimization framework. The complete 4D graph corresponding to a DCE-MRI sequence is reduced to a concatenation of minimum spanning trees, which can be optimized more efficiently. To address the changes due to contrast, a data cost function which incorporates pharmacokinetic modelling information is formulated. The advantages of this method are demonstrated on 8 DCE-MRI image sequences of patients with advanced rectal tumours, presenting mild to severe motion.
| Original language | English |
|---|---|
| Pages (from-to) | 73-84 |
| Number of pages | 12 |
| Journal | Lecture Notes in Computer Science (including subseries Lecture Notes in Artificial Intelligence and Lecture Notes in Bioinformatics) |
| Volume | 8677 |
| DOIs | |
| State | Published - 2014 |
| Externally published | Yes |
UN SDGs
This output contributes to the following UN Sustainable Development Goals (SDGs)
-
SDG 3 Good Health and Well-being
Fingerprint
Dive into the research topics of 'An MRF-based discrete optimization framework for combined DCE-MRI motion correction and pharmacokinetic parameter estimation'. Together they form a unique fingerprint.Cite this
- APA
- Author
- BIBTEX
- Harvard
- Standard
- RIS
- Vancouver