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Quantitative impact of Dixon mumap variability in dual-time-point brain PET/MR
Jackson, Kimberly; Bartlett, Rachel; Friedman, Kent; Shepherd, Timothy; Koesters, Thomas; Teruel, Jose; Fenchel, Mathias; Hermosillova-Valadez, Gerardo; Faul, David; Boada, Fernando
PMCID:4798694
PMID: 26956335
ISSN: 2197-7364
CID: 2023522
Inhomogeneous static magnetic field-induced distortion correction applied to diffusion weighted MRI of the breast at 3T
Teruel, Jose R; Fjøsne, Hans E; Østlie, Agnes; Holland, Dominic; Dale, Anders M; Bathen, Tone F; Goa, Pål E
PURPOSE/OBJECTIVE:To evaluate the performance of an advanced method for correction of inhomogeneous static magnetic field induced distortion in echo-planar imaging (EPI), applied to diffusion-weighted MRI (DWI) of the breast. METHODS:An algorithm for distortion correction based on the symmetry of the distortion induced by static field inhomogeneity when the phase encoding polarity is reversed was evaluated in 36 data sets of patients who received an MRI examination that included DWI (b = 0 and 700 s/mm(2) ) and an extra b = 0 s/mm(2) sequence with opposite phase encoding polarity. The decrease of the L2 -square norm after correction between opposed phase encoding b = 0 images was calculated. Mattes mutual information between b = 0 images and fat-suppressed T2 -weighted images was calculated before and after correction. RESULTS:The L2 -square norm between different phase encoding polarities for b = 0 images was reduced 94.3% on average after distortion correction. Furthermore, Mattes mutual information between b = 0 images and fat-suppressed T2 -weighted images increased significantly after correction for all cases (P < 0.001). CONCLUSION/CONCLUSIONS:Geometric distortion correction in DWI of the breast results in higher similarity of DWI to anatomical non-EPI T2 -weighted images and would potentially allow for a more reliable lesion segmentation mapping among different MRI modalities.
PMID: 25323982
ISSN: 1522-2594
CID: 4004122
Dynamic contrast-enhanced MRI texture analysis for pretreatment prediction of clinical and pathological response to neoadjuvant chemotherapy in patients with locally advanced breast cancer
Teruel, Jose R; Heldahl, Mariann G; Goa, PÃ¥l E; Pickles, Martin; Lundgren, Steinar; Bathen, Tone F; Gibbs, Peter
The aim of this study was to investigate the potential of texture analysis, applied to dynamic contrast-enhanced MRI (DCE-MRI), to predict the clinical and pathological response to neoadjuvant chemotherapy (NAC) in patients with locally advanced breast cancer (LABC) before NAC is started. Fifty-eight patients with LABC were classified on the basis of their clinical response according to the Response Evaluation Criteria in Solid Tumors (RECIST) guidelines after four cycles of NAC, and according to their pathological response after surgery. T1 -weighted DCE-MRI with a temporal resolution of 1 min was acquired on a 3-T Siemens Trio scanner using a dedicated four-channel breast coil before the onset of treatment. Each lesion was segmented semi-automatically using the 2-min post-contrast subtracted image. Sixteen texture features were obtained at each non-subtracted post-contrast time point using a gray level co-occurrence matrix. Appropriate statistical analyses were performed and false discovery rate-based q values were reported to correct for multiple comparisons. Statistically significant results were found at 1-3 min post-contrast for various texture features for the prediction of both the clinical and pathological response. In particular, eight texture features were found to be statistically significant at 2 min post-contrast, the most significant feature yielding an area under the curve (AUC) of 0.77 for response prediction for stable disease versus complete responders after four cycles of NAC. In addition, four texture features were found to be significant at the same time point, with an AUC of 0.69 for response prediction using the most significant feature for classification based on the pathological response. Our results suggest that texture analysis could provide clinicians with additional information to increase the accuracy of prediction of an individual response before NAC is started.
PMID: 24840393
ISSN: 1099-1492
CID: 4004112