A multicompartment model for intratumor tissue-specific analysis of DCE-MRI using non-negative matrix factorization
- PMID: 33608885
- DOI: 10.1002/mp.14793
A multicompartment model for intratumor tissue-specific analysis of DCE-MRI using non-negative matrix factorization
Abstract
Purpose: A pharmacokinetic analysis of dynamic contrast-enhanced magnetic resonance imaging (DCE-MRI) data is subject to inaccuracy and instability partly owing to the partial volume effect (PVE). We proposed a new multicompartment model for a tissue-specific pharmacokinetic analysis in DCE-MRI data to solve the PVE problem and to provide better kinetic parameter maps.
Methods: We introduced an independent parameter named fractional volumes of tissue compartments in each DCE-MRI pixel to construct a new linear separable multicompartment model, which simultaneously estimates the pixel-wise time-concentration curves and fractional volumes without the need of the pure-pixel assumption. This simplified convex optimization model was solved using a special type of non-negative matrix factorization (NMF) algorithm called the minimum-volume constraint NMF (MVC-NMF).
Results: To test the model, synthetic datasets were established based on the general pharmacokinetic parameters. On well-designed synthetic data, the proposed model reached lower bias and lower root mean square fitting error compared to the state-of-the-art algorithm in different noise levels. In addition, the real dataset from QIN-BREAST-DCE-MRI was analyzed, and we observed an improved pharmacokinetic parameter estimation to distinguish the treatment response to chemotherapy applied to breast cancer.
Conclusion: Our model improved the accuracy and stability of the tissue-specific estimation of the fractional volumes and kinetic parameters in DCE-MRI data, and improved the robustness to noise, providing more accurate kinetics for more precise prognosis and therapeutic response evaluation using DCE-MRI.
Keywords: dynamic contrast-enhanced magnetic resonance imaging (DCE-MRI); non-negative matrix factorization (NMF); tissue-specific analysis; tumor heterogeneity.
© 2021 American Association of Physicists in Medicine.
References
REFERENCES
-
- Jahani N, Cohen E, Hsieh M, et al. Prediction of treatment response to neoadjuvant chemotherapy for breast cancer via early changes in tumor heterogeneity captured by DCE-MRI registration. Sci Rep. 2019;9:12114.
-
- Liang J, Cheng Q, Huang J, et al. Monitoring tumour microenvironment changes during anti-angiogenesis therapy using functional MRI. Angiogenesis. 2019;22:457-470.
-
- Payan N, Presles B, Brunotte F, et al. Biological correlates of tumor perfusion and its heterogeneity in newly diagnosed breast cancer using dynamic first-pass 18 F-FDG PET/CT. Eur J Nucl Med Mol Imaging. 2020;47:1103-1115.
-
- Mahrooghy M, Ashraf A, Daye D, et al. Pharmacokinetic tumor heterogeneity as a prognostic biomarker for classifying breast cancer recurrence risk. IEEE Trans Biomed Eng. 2015;62:1585-1594.
-
- Jiřík R, Taxt T, Macicek O, et al. Blind deconvolution estimation of an arterial input function for small animal DCE-MRI. Magn Reson Imaging. 2019;62:46-56.
MeSH terms
Substances
Grants and funding
LinkOut - more resources
Full Text Sources
Other Literature Sources
Medical