With MRI being increasingly incorporated in the radiotherapy workflow, the multidisciplinary community has a strong interest in developing “4D-MRI” techniques for both offline (tumor motion characterization for treatment planning) and online (tumor motion tracking) applications. In a cohort of 10 volunteers, the present study applied 2D (coronal) bSSFP with interleaved cylindrical navigators monitoring the liver dome to retrospectively derive 4D-MRI comparing two sorting methods, namely phase and amplitude-probability. Amplitude-probability binning was shown, both qualitatively and quantitatively, to reduce “volume inconsistencies” caused by variable breathing.
MRI
Ten normal volunteers consented for an IRB-approved study and were imaged coronally under free breathing conditions on a 3T widebore system (MR750w, GE Healthcare, Waukesha, WI) using a 2D balanced steady-state free precession (bSSFP) sequence including cylindrical navigator echoes interleaved between successive image frames5. Navigators were positioned to monitor the liver dome craniocaudally. To allow for sufficient sampling of 10 reconstructed 4D/respiratory bins, 30 cine images were acquired at each slice location (all dynamics acquired before moving to the next slice location)6,7. The FOV included the lungs/upper-abdomen (3602-4202 mm2 on matrix of 192×192 or 200×200) with a slice profile thickness of 5mm. Repetition time (frame rate) spanning single-shot bSSFP+navigator waveforms varied from 383-493ms with a flip angle of 35°. The first two volunteers’ exam included 17 slices; the remaining eight volunteers’ exams included either 31 or 33 slices.
Retrospective Sorting
Retrospective, single-pass sorting and slice stacking was performed using in-house software (Matlab, The Matworks, Inc., Natick MA) and DICOM 2D images. Navigator profiles (from an acquisition log file) were analyzed to determine the dome/edge position or equivalent mathematical surrogate (Figure 1a). Subsequently, timing information (from an additional log file) was used to interpolate this set of surrogate positions onto a uniform temporal grid synchronized with imaging. (Herein, spline interpolation was employed with 4× temporal upsampling to improve inspiratory peak localization). Respiratory bin values (computed as continuous variables) per time point were determined using two methods – standard phase and amplitude-probability2,8 (Figure 1c). Amplitude-probability binning involved generating dome/surrogate position distributions for inhalation and exhalation and asserting that each bin spans an equal-area portion of said distribution (hence equal-probability) (Figure 1b). DICOM tag TriggerTime was referenced to assign a continuous phase and amplitude-probability bin value per 2D image. 2D image selection for phase- and amplitude-probability-4D-MRI was based on continuous bin values being nearest the given central bin value.
Volume Consistency Analyses
Volume consistency of phase- versus amplitude-probability-4D-MRI was assessed both qualitatively and quantitatively. Qualitative inspection was carried out via visual comparison of side-by-side sagittal and axial 3D cut-planes at the liver dome position for the three bins closest to peak inhalation (10,1,2). Quantitative analyses incorporated 11 contiguous sagittal cut-planes: within a 2D ROI that encompassed the liver dome and was common over all slices and bins for a given volunteer, the anterior-posterior (x) directional image (≡I) gradient magnitude image (≡|dI/dx|) was calculated using Matlab function imgradientxy (Figure 2a). A mean anterior-posterior image gradient magnitude (≡mean|dI/dx|) was derived by averaging over all pixels and over 11 slices; this calculation was tallied for each respiratory bin. To remove the signal bias introduced by motion of anatomy relative to fixed 2D ROI selection, mean|dI/dx| for phase-based sorting (≡mean|dI/dx|phase) was normalized by the same result for amplitude-probability sorting, per bin.
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