Elena A Kaye1, Kristin L Granlund2, Stephen B Solomon2, and Majid Maybody2
1Medical Physics, Memorial Sloan Kettering Cancer Center, New York, NY, United States, 2Radiology, Memorial Sloan Kettering Cancer Center, New York, NY, United States
Synopsis
Acquisition of a viable tissue sample is critical to success
of a biopsy. DWI could help differentiate between viable and necrotic tissue
during the procedure, however, EPI-DWI is not suitable in a percutaneous-biopsy
setting due to geometric distortions. DW Dual Echo Steady State (DESS) sequence
allows acquisition of 3D undistorted DWI images. This study evaluated the application
of DW-DESS during an MR-guided liver biopsy in two patients. Using single
breath-hold acquisition, DW-DESS image depicted a liver lesion sharper and less
distorted than EPI-DWI. DW-DESS also allowed DWI in the presence of a biopsy
needle without distortions of EPI. Introduction
Acquisition
of a viable tissue sample is critical to success of percutaneous biopsy. MRI offers a
unique diffusion-weighted imaging (DWI) contrast mechanism sensitive to
microstructural tissue properties and that differentiates between viable and
necrotic tissue
1. Unfortunately,
the commonly used echo planar imaging (EPI) DWI technique is not well-suited
for biopsy. The EPI geometric distortions of patient's anatomy result in an erroneous
impression of the relative position between the tumor and the needle entry
point. Furthermore, the artifact produced by a biopsy needle makes the DWI
image difficult to interpret and to guide further needle advancement. Hence, the
DW-PROPELLER technique, much less sensitive to local magnetic field variations
and motion than EPI, was previously proposed for biopsy guidance and the feasibility
of selective positioning of a biopsy needle within a viable region of the tumor
was demonstrated in a VX2 rabbit tumor model
1. However, despite
the benefits of the DW-PROPELLER, long acquisition time of this technique
diminishes its role in an interventional setting. DW Dual Echo Steady State (DW-DESS)
sequence
2, on the other hand, allows acquisition of 3D high resolution DW images
without EPI distortions and requires shorter acquisition times compared to
PROPELLER. Motion
sensitivity of DESS, however, precluded the development of this technique in the
abdomen
2-4.
Motivated by successful application of DESS in a motion susceptible setting,
e.g., breast imaging
2, the study aimed to
evaluate the application of DW-DESS during an MR-guided liver biopsy.
Methods
This
study was approved by the institutional review board. All
human subjects were scanned with written, informed consent. Imaging was
performed on a GE 1.5 T MR450w scanner (GE Healthcare, Waukesha, WI) using a
12-channel phased-array torso Radiofrequency coil. The diffusion sensitivity of
the DESS sequence was adjusted by modifying the spoiler gradient area in the
slice direction. Imaging in a volunteer liver was used to determine parameters
enabling a single breath-hold image acquisition. The motion artifacts were
compared between sequential and elliptic-centric phase encode ordering. Patient
scans were carried out in two subjects undergoing routine MR-guided liver
biopsy using a titanium-alloy 16G coaxial introducer needle and an 18G
semi-automatic biopsy gun (InVivo, Germany). An interventional
radiologist navigated the needle to the target using intra-procedural imaging
with LAVA-Flex sequence without a breath-hold in subject 1 and with a breath-hold
in subject 2. Breath-hold DESS images were acquired before and after the biopsy
needle was introduced in patients 1 and 2, respectively. In patient 1, a DW-DESS
image of a lesion was compared to a previously-obtained diagnostic EPI-DWI. In
patient 2, lesion appearance in the presence of biopsy needle and the artifact
of the needle were compared between DESS and LAVA (no EPI-DWI images were available). No
fat suppression was applied in DW-DESS. Table 1 summarizes patient
details and imaging parameters.
Results
The application of DESS to image the liver
in a volunteer showed that using an acquisition matrix of 256x160x16 with
minimum repetition time, scan time could be reduced to 27 seconds, enabling
single breath-hold image acquisition. Motion artifacts present in the second
echo (TE2) image during a breath-hold acquisition with a spoiler area of 2
cycles per voxel (Figure 1) showed the benefit of elliptic-centric phase
ordering compared to sequential ordering. The boundaries of a cyst could be
well-delineated in both cases. In patient 1, compared to the diagnostic EPI-DWI
image, the lesion appeared sharper, less blurred and distorted on the high DW DESS
image (Figure 2). Decreased signal intensity area was observed posterior to the
tumor (Figure 2c), potentially due to bulk motion. In patient 2, the biopsy needle
artifact seen in a high DW DESS image was found comparable to the one in the
LAVA-Flex image (Figure 3). Moreover, despite the small size of the tumor, the position
of the biopsy needle could be clearly visualized on the DW-DESS image.
Discussion
In
this study, we performed a preliminary qualitative evaluation of DW-DESS in a
setting of MRI-guided liver biopsy. The demonstrated capability to acquire a DW
image during a single breath-hold makes DESS a feasible technique for DWI of the
abdomen. Similar to breath-hold imaging in general, successful DESS imaging
will be limited by the patient’s ability to follow breath-hold instruction,
sometimes impaired in sedated patients. Diffusion sensitivity of DESS will be
optimized in future patients to demonstrate differentiation between viable and
necrotic tissue.
Conclusion
The
lack of geometric distortion, higher resolution, acceptable biopsy needle
artifact and short acquisition times of DW-DESS can help transform MRI-guided
biopsy from a macroscopically to a microscopically targeted procedure and reduce biopsy
sampling errors.
Acknowledgements
We acknowledge Dr. Marcus Alley for providing the DW-DESS pulse sequence.References
1. J. Deng, S. Virmani, G. Y. Yang et al, JMRI 30 (2), 366-373 (2009).
2. K. L.
Granlund, E. Staroswiecki, M. T. Alley, B. L. Daniel and B. A. Hargreaves,
Magnetic resonance imaging 32 (4),
330-341 (2014).
3. E.
Staroswiecki, K. L. Granlund, M. T. Alley, G. E. Gold and B. A. Hargreaves,
Magnetic Resonance in Medicine 67
(4), 1086-1096 (2012).
4. B. L. Daniel, K. L. Granlund, C. J. Moran et al, European journal of
radiology 81, S24-S26 (2012).