Junzhou Chen1,2, Pei Han1,2, Fei Han3, Zhehao Hu1,2, Nan Wang1,2, Wensha Yang4, Anthony G Christodoulou1,2, Debiao Li1,2, and Zhaoyang Fan1,2,5
1Biomedical Imaging Research Institute, Cedars-Sinai Medical Center, Los Angeles, CA, United States, 2Department of Bioengineering, University of California, Los Angeles, Los Angeles, CA, United States, 3Siemens Medical Solutions USA, Inc., Los Angeles, CA, United States, 4Department of Radiation Oncology, University of Southern California, Los Angeles, CA, United States, 5Department of Radiology, University of Southern California, Los Angeles, CA, United States
Synopsis
MRI can provide superior soft tissue contrasts for radiation therapy planning. However, radiation planning in the abdomen is especially difficult because respiratory motion can cause misregistration across separate scans with different contrast weightings due to inconsistent breath holds or poor patient compliance. While some studies have produced volumetric and motion-resolved images, they are all limited to a single contrast which is suboptimal for radiation planning. To address these issues, we present a free-breathing MR imaging platform that produces multi-contrast and motion-resolved volumetric images using MR-multitasking, dedicated for radiation therapy planning, and under a 9:30 mins scan time.
Introduction
Imaging simulation, is an essential step of radiation
treatment planning. For better delineation of the target and organs-at-risk
(OARs), MR has increasingly been adopted as a
simulation platform complementary to CT. Despite demonstrated successes in many
other disease sites, MR simulation is challenging in the mobile abdominal site because
1) multi-contrast images (useful for differentiating multiple OARs or the
target) are typically acquired in separate scans with unmatched parameters or
varied motion compensation strategies, and are susceptible to inter-scan misalignment;
2) image quality of breath-hold scans can be severely degraded in patients with
poor compliance or limited breath-hold capacity; 3) existing 4D MR (i.e. motion
resolved volumetric imaging for better understanding of target motion)
techniques are all limited to a single contrast weighting 1-4,
which may be suboptimal for target delineation. In this work, we present a standalone
MR simulation technique that accomplishes multiple tasks: to provide
multiple, dynamic contrast weightings with inherent spatial co-registration and
to provide motion-resolved volumetric images.Method
Sequence Design:
As shown in Fig. 1, each repetition time (TR) of our multi-task
(MT) MR sequence starts with a saturation recovery (SR) pulse followed by a
group of FLASH readouts during T1 recovery, a short temporal gap, and a second
and third group of FLASH readouts before and after T2-preparation,
respectively. K-space is sampled with a Cartesian spiral-in pattern (Fig. 1B)
with 10 lines in each spiral arm and the 10th line being the k-space
center and used as the navigator. This sampling pattern allows for 1) a more
densely sampled k-space center region but faster reconstruction time compared to radial sampling and 2) reduced eddy current effects
and thus high-quality navigator and images due to smaller k-space jumps when the k-space center is sampled 5,6.
Image reconstruction framework:
Using MR Multitasking7 (MT), a low-rank tensor (LRT) technique, we can efficiently encode an image
function of these multiple MR spatiotemporal dimensions (i.e. physical
dimensions, motion, contrast) into linear combinations of the spatial
coefficients $$$\mathbf{U}_\mathbf{r}$$$ , as shown in fig. 1C. In this case, $$ \mathcal{A}\ =\mathcal{G}\ \times_1\mathbf{U}_\mathbf{r}\times_2\mathbf{U}_{motion}\times_3\mathbf{U}_{contrast}$$
Where $$$\mathcal{A}$$$ is the tensor
representing a multidimensional image A(r,$$$t_{motion}$$$, $$$t_{contrast}$$$) with r being the physical dimensions [x,y,z],
and $$$t_{motion}$$$, $$$t_{contrast}$$$ being the temporal
dimensions. The $$$\mathbf{U}$$$ matrices contain basis functions
for each dimension, and $$$\mathcal{G}$$$ is the core tensor. A combined temporal factor $$$\mathrm{\Phi}=\mathcal{G}\times_2\mathbf{U}_{motion}\times_3\mathbf{U}_{contrast}$$$ is
determined from Bloch-constrained low-rank tensor completion and motion binning
from the navigator data. We then determine $$$\mathbf{U}_\mathbf{r}$$$ by$$
\hat{\mathbf{U}}_\mathbf{r} = \underset{\mathbf{U}_\mathbf{r}}{\arg\min} \|d-\Omega(\Phi \times_1 E \mathbf{U}_\mathbf{r})\|^2_2
$$
where $$$\mathbf{d}$$$ contains the
measured imaging data, $$$\Omega$$$ is the
spiral-in Cartesian sampling operator, $$$\mathbf{E}$$$ is the
multi-channel spatial encoding operator, and $$$\lambda$$$ is the Lagrange
multiplier for $$$R\left(\mathbf{U}_\mathbf{r}\right)$$$, a wavelet regularizer.
Experiments:
The MT-MR sequence was evaluated through in-silico and
in-vivo experiments, using following imaging parameters: coronal orientation, FOV
= 256(SI) x 358(LR) x 256(AP) mm3, resolution = 1.6 x 1.6 x 3.2(interpolated
to 1.6) mm3, echo spacing/TE = 6/2.62 ms, gap time = 700ms, total scan time = 9:30min.
3D images were reconstructed with 8 motion phases.
We first simulated the sequence using the digital abdomen
motion phantom developed by Lo et al.8,9
The quality of reconstructed images were evaluated against the “digital truth”
of the phantom by 1) visually comparing contrast weightings and liver dome’s locations
at motion state 1 and 8 and 2) calculating structural similarity (SSIM) maps
(structural component) between MT-MR images and the ground truth at motion
state 8 (end-exhalation).
We also performed testing on 6 healthy volunteers on a 3T system (MAGNETOM Vida, Siemens Healthcare, Erlangen, Germany). During the scan, volunteers
were instructed to lie still and breathe normally. Repeated free-breathing MR
images (>1 fps) of a 2D coronal slice were acquired to provide motion
references in 3 subjects. The ranges of respiratory motion measured at the liver
dome were compared between MT-MR and the reference method.Results
In silico
Fig. 2 shows the reconstructed results from the digital
phantom simulations at motion state 1 and 8 across 3 contrast points, along
with their respective digital truth. MT-MR provided visually comparable
contrast weightings and liver locations when compared to the digital truths. The
structural SSIM maps show that our reconstruction algorithm was successful in recovering
the majority of anatomical structures, although most structural differences
occur at organ boundaries, likely due to edge blurring.
In vivo
Fig. 3 showcases the capabilities of our MT-MR technique. One
may visualize abdominal structures in a flexible fashion because of the
availability of volumetric, motion-resolved, multi-contrast images. The
differences in motion ranges of the liver dome between MT-MR and 2D references were
within 0.2 mm (Fig. 4A). Fig. 4B shows the matched liver locations from
volunteer 1 between MT-MR and the 2D reference images. Discussion
In this work, we developed an MT-MR simulation technique
that provides respiratory motion-resolved, spatially co-registered multi-contrast,
and volumetric MR images for abdominal radiation treatment planning. Its
technical feasibility was demonstrated on a digital phantom and healthy
volunteers. There is still room to further improve spatial resolution. More importantly, the technique needs to be validated in
patients receiving radiation therapy. In conclusion, MT-MR is technically
feasible in serving MR simulation in abdominal radiation treatment planning.Acknowledgements
This work is supported by NIH grant NIH/NIBIB R01EB029088References
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