Jorge E Jimenez1, Leah C Henze Bancroft2, Roberta Strigel1,2,3, Kevin M Johnson1, Scott B Reeder1,2,4,5,6, and Walter F Block1,2,4
1Department of Medical Physics, University of Wisconsin-Madison, Madison, WI, United States, 2Department of Radiology, University of Wisconsin School of Medicine and Public Health, Madison, WI, United States, 3Carbone Cancer Center, University of Wisconsin-Madisonsin, Madison, WI, United States, 4Department of Biomedical Engineering, University of Wisconsin-Madison, Madison, WI, United States, 5Department of Medicine, University of Wisconsin School of Medicine and Public Health, Madison, WI, United States, 6Department of Emergency Medicine, University of Wisconsin School of Medicine and Public Health, Madison, WI, United States
Synopsis
In this work, we show the value of a
digital phantom to evaluate a dynamic reconstruction. We evaluated the fidelity
of the reconstruction using SSIM measurements from simulations and three
patients to support conclusions derived from the digital phantom. The highly
configurative characteristics of the in-silico platform provide a tool for
other researchers to test, evaluate and compare their own acquisition and
reconstruction techniques.
Introduction
A significant gap exists in the ability
to validate and compare the plethora of constrained reconstruction
methodologies being applied to DCE-MRI of cancerous lesions. Considerable
difficulty, time and expense is incurred identifying appropriate subjects with
the desired range in morphological and temporal enhancement patterns while also
identifying a gold standard for the actual spatial and temporal enhancement pattern
of each subject. We integrate digital components to create spatially and
temporally realistic breast lesions and merge them into realistic breast
background tissue. The purpose of this work is to demonstrate utility of the in
silico platform by evaluating an extended version of the dynamic reconstruction
from our previously presented abbreviate DCE breast MRI protocol1.Methods
A digital breast phantom tool has been
developed at our institution2-4
that creates variants of breast lesions with reasonable morphology and
enhancement patterns derived from user-selected pharmacokinetic parameters, as
shown in Figure 1. Raw data in the
ISMRMRD format is generated to simulate data weighted by user-specified coil
sensitivity maps, acquired along user-specified trajectories, and degraded by
realistic noise.
We generated raw data to simulate four lesion
variants (Figure 3) merged into a realistic breast background being acquired by
a 3D radial mask-subtracted (SVIPR) trajectory. To simplify analysis, a
step-function transition was used in the two spatially heterogeneous lesions
between the core and ring-enhancing region.
We evaluated the utility of the digital
phantom by evaluating:
- A new reconstruction methodology we developed
that dovetails with 3D radial acquisitions, Spatial CS with Temporal
Local Low-Rank assistances—STELLR
(Figure 2).
- A simple Parallel Imaging reconstruction (PILS)5-based strategy.
STELLR exploits sparsity created by
pre-contrast mask-subtraction, a spatial constraint and local low-rank
constraint in the temporal dimension to produce bilateral breast images with 10
second frame rates and 0.83 mm resolution. In vivo STELLR studies were used to
assure that the stochastic noise level in the digital simulation was
representative of actual scans. We benchmarked the temporal and spatial
fidelity of both methods by computing the global value and similarity image of
the Structural Similarity Index Measurements (SSIM) 6,7.
In-vivo comparison: Three patients
consented to a research DCE MRI, IRB-approved, HIPAA compliant study using a
16-channel breast coil (Discovery 750 3T, GE Healthcare) over a 32 cm FOV. SVIPR,
a T1-weighted 3D radial trajectory8 with four unique
echoes was used to acquire one pre- and one post-contrast phase, each 3 minutes
long (Fig. 2a).
Results
PILS reconstruction failed to provide a proper
visualization of the expected enhancement pattern. On the contrary, the dynamic
non-linear STELLR approach was able to overcome the significant data
undersampling (45x acceleration). The STELLR reconstruction provided detailed
visualization of homogeneous and heterogeneous lesions morphology. The value of
the SSIM similarity image is demonstrated in the bottom row of Figure 3, where
the darkened regions in the speculated lesion show the difficulty in accurately
depicting the rim enchainment in this challenging lesion. The digital phantom
successfully mimicked in vivo performance, as shown in the comparison of
in-vivo and in silico enhancement in Figure 4. STELLR relies on mask subtraction
to increase sparsity and achieved maximum performance. Finally, in vivo reconstructions
of a volunteer in Figure 5 showing morphologic details of a known breast
cancer, including spiculated margins and an irregular shape corroborate the digital
phantom’s predicted performance. Discussion
Due to the lack of a gold standard for high
temporal resolution dynamic reconstructions, definitive validation of temporal
and spatial performance claims is difficult. Some groups have shown the value
of physical phantoms9,10
and a dynamic digital phantom11 to
accelerate and ensure validation of new MR techniques using realistic digital
imaging features and kinetic behavior. The advanced digital phantom described
here could evaluate new acquisition and reconstruction performance for depicting
specific in vivo physiology and/or heterogeneous treatment response prior to
undergoing the expense and efforts of clinical trials. The highly configurative characteristics
of the digital phantom and its ISMRM compatible formats will allow us
and others to compare reconstruction methods within and across institutions.Conclusion
We demonstrated the value of a digital phantom
to evaluate the performance of the SVIPR STELLR approach. The in-silico
simulation allowed for quantitative measurements. The in-silico platform can be
configured or adapted to other scenarios to satisfy researcher’s necessities
beyond clinical evaluation of new DCE-MRI methods. Acknowledgements
Research supported by NIH
R25 GM083252, K24 DK102595, T32CA009206, and F31CA217160, RSNA Research &
Education Foundation, the Department of Radiology R & D Fund at the
University of Wisconsin, Wisconsin Women's Health Foundation, the Science and
Medicine Graduate Research Scholars and GE Healthcare.References
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