Bjorn Stemkens1, Rob HN Tijssen1, Jan JW Lagendijk1, and Cornelis AT van den Berg1
1Department of Radiotherapy, University Medical Center Utrecht, Utrecht, Netherlands
Synopsis
Geometric accuracy is vital for MR-guided
radiotherapy. In this study we quantify
the geometric fidelity of a retrospectively sorted 4D-MRI and 2D MS cine-MR
acquisition, which serve as input for a motion model for dose accumulation
mapping and tumor tracking. A linearly moving MRI-compatible motion phantom was
used to quantify the positional error in the 4D-MRI and 2D MS acquisitions
using a range of user-defined motion trajectories.
Geometrical errors were found
to be smaller than the voxel or pixel size.Purpose
MRI is becoming a prominent
imaging technique in the field of external beam radiotherapy, for both
radiation therapy treatment planning and, with the recent introduction of the
MR-Linac
1, for guidance during radiation. However, geometric
accuracy is vital for correct delineations pre-treatment and accurate tumor
tracking during radiation. Previously, we have implemented a motion model
approach for dose accumulation mapping and tumor tracking during radiotherapy
treatment
2. The method determines the current 3D motion state of the
abdomen, based on 1) a statistical motion model derived from a retrospectively
sorted 4D-MRI acquired prior to treatment
3, and 2) fast 2D cine-MR
images acquired during the treatment. The current motion state is estimated by
co-registering the incoming 2D data to a 3D volume that is deformed based on
the predetermined statistical model
4. For an accurate calculation of
the accumulated dose, it is essential that the estimated motion states are
geometrically accurate. Here, we quantify the geometric fidelity of 1) the
retrospectively sorted 4D-MRI and 2) the 2D cine-MR images using an
MR-compatible motion phantom. This was achieved by moving the phantom using a
range of user-defined waveforms while acquiring 4D-MRI and 2D cine-MR data and
comparing the 4D and 2D positions with reference positions.
Methods
Acquisitions:
All acquisitions were performed on a 1.5T MR scanner (Ingenia, Philips, Best,
Netherlands). 4D-MRI data were acquired using a 3D RF-spoiled GRE with radial
in-plane sampling (parameters in Table 1)
interleaved with a navigator. Moreover, two orthogonal (coronal and sagittal)
2D cine-MRI slices (see Fig. 1c)
were acquired in an interleaved fashion (parameters in Table 1). Additionally, static 3D volumes were acquired using the
same parameters used for the 4D-MRI, which served as reference images for the
various positions of the motion phantom.
Experimental set-up: An elliptically shaped motion phantom (Quasar, Modus Medical Devices
Inc., London, Canada) was used that consists of two static compartments and one
linearly moving cylinder, which was driven by user-defined waveforms (see Fig. 1a, b). The static parts were
filled with CuSO4-doped water, while the moving cylinder was filled
with doped agarose gel. A Ping Pong ball, simulating a tumor, was filled with
CuSO4-doped water and inserted in the center of the cylinder. Four
4D-MRI and nine 2D data sets were acquired, while the cylinder was moving in a
1D linear fashion using the waveforms described in Table 2. The 4D-MRI waveforms were used to test the hypothesis that
the 4D-MRI acquisition depicts the average position within every phase for
various motion amplitudes. The nine 2D waveforms represent all expected motions
within the abdomen.
Analysis: 4D-MRIs
were constructed by retrospectively sorting the 4D data into ten respiratory
phases through phase binning. Based on the user-defined waveforms, the average
position of the ball for every phase was calculated, which are the
geometrically correct (GC) positions. Next, the GC positions within the images
were calculated using the static (reference) 3D acquisitions. The difference in
center of mass (COM) of these positions and the positions in the 4D-MRI data
sets were calculated as a measure for the geometrical error of the 4D-MRI. Finally,
rigid registration was performed for all 2D MS acquisitions and the
root-mean-squared error (RMSE) and normalized RMSE (NRMSE) between the estimated
translations and the user-defined waveforms were calculated.
Results and Discussion
The differences between the
positions determined by the navigator and the waveforms were smaller than 1 mm.
Fig. 2 displays one of the
calculated 4D motion trajectories in blue. Moreover, for every phase a boxplot
is plotted, which was calculated using the different positions in that phase,
indicating that the 4D-MRI depicts correct positions,
despite large intra-phase variation. The
average differences in COM over the ten phases for the four 4D-MRI acquisitions
were 1.03, 1.30, 0.96 and 1.25 mm respectively, which resembles the average
geometrical error for the 4D-MRI.
Fig. 3
shows a coronal view of the phantom at different positions (left) and the
corresponding phases of the 4D-MRI. The red lines are a visual aid for
corresponding positions. The average RMSE for the 2D MS acquisitions was 1.06
mm, corresponding to an NRMSE of 4.9%. The acquisition with the frequency sweep
waveform showed that the images depict the correct position for sinusoidal
motion up to 0.5Hz.
Conclusion
Using a linear MRI-compatible motion phantom the
geometric errors of a retrospectively sorted 4D-MRI (1-1.3 mm) and a 2D MS
acquisition (0.6-1.5 mm), which serve as input for a motion framework, were
calculated and found to be smaller than the voxel/pixel size. Future studies
will focus on phantom motions in more directions, to simulate more
representative in-vivo motion
trajectories.
Acknowledgements
No acknowledgement found.References
[1] Lagendijk JJW, Raaymakers BW, van den Berg CAT,
et al. MR guidance in radiotherapy, PMB, 2014;59:R349-R369
[2] Stemkens B,
Tijssen RHN, de Senneville BD, et al. Estimating dynamic 3D abdominal motion
for radiation dose accumulation mapping using a PCA-based model and 2D
navigators, ISMRM 2015, #3679
[3] Stemkens B, Tijssen RHN, de Senneville BD, et
al. Optimizing 4D MRI data sampling for respiratory motion analysis of
pancreatic motion, IJROBP, 2015;91(3):571-578
[4] King AP, Buerger C, Tsoumpas
C, et al. Thoracic respiratory motion estimation from MRI using a statistical
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