Marnix C. Maas1, Patrik Zámecnik1, Moritz J. Schneider2,3, Thomas Gaass2,4, Thomas Benkert5, Julien Dinkel2,4, and Tom W.J. Scheenen1
1Medical Imaging, Radboudumc, Nijmegen, Netherlands, 2Comprehensive Pneumology Center, German Center for Lung Research (DZL), Munich, Germany, 3Antaros Medical AB, Mölndal, Sweden, 4Department of Radiology, University Hospital, LMU Munich, Munich, Germany, 5MR Application Predevelopment, Siemens Healthcare GmbH, Erlangen, Germany
Synopsis
Detection
of lymph node (LN) metastases can be improved using Ferumoxtran-10, an ultrasmall
superparamagnetic particles of iron oxide (USPIO) contrast agent . Commonly, T2* contrast is used to distinguish between normal LNs (high USPIO
uptake, low signal) and metastases (low uptake, high signal). T1-weighted imaging
may offer complementary information, but is challenging because of the strong
T2* effects of the contrast agent. This work investigates whether ultrashort
echotime (UTE) imaging with a stack-of-spirals sequence can mitigate this issue. High-resolution
USPIO-enhanced T1-weighted UTE of the pelvis was achieved, and T1-mediated signal
hyperintensities were indeed observed in LNs in patients with prostate cancer.
Introduction
Detection
of pelvic lymph node (LN) metastases can be improved using the ultrasmall
superparamagnetic particles of iron oxide (USPIO) contrast agent Ferumoxtran-101. The contrast agent accumulates in healthy lymph
nodes through uptake by cells of the immune system, while in metastatic LNs particle
accumulation is much lower. USPIO-enhanced MRI for detection of LN metastases
is usually based on T2*-weighted (T2*w) imaging, in which LNs with high USPIO uptake exhibit signal
loss while LNs with low uptake retain a high signal intensity. T1-weighted
imaging may offer complementary information to T2*-weighted imaging in this
context, as the R1 and R2* relaxivities of Ferumoxtran-10 differ in their
dependency on the microscopic distribution of the USPIO nanoparticles2. Thus, T1w imaging may potentially aid in
improving the specificity of USPIO enhanced LN diagnostics. However, obtaining
unambiguous USPIO-enhanced T1 contrast is challenging using conventional echo-type
sequences, because of the strong T2* effect of the contrast agent. Ultrashort echo
time (UTE)-type sequences may mitigate this issue by minimizing T2* relaxation effects.
Before any additional value of T1w UTE for LN diagnostics can be investigated,
the feasibility of obtaining the desired contrast at sufficiently high
resolution3 and image quality must be established. Therefore,
the purpose of this study was to assess whether T1-mediated signal enhancement
due to USPIO uptake can be observed in pelvic lymph nodes in prostate cancer
patients at high isotropic spatial resolution using a stack-of-spirals UTE
sequence.Methods
All
measurements were performed on a 3T system (MAGNETOM PrismaFit, Siemens Healthcare,
Erlangen, Germany) with standard body and spine phased array coils. The prototypical
UTE sequence used a stack-of-spirals k-space trajectory with non-selective
excitation and variable-duration slice encoding to minimize the effect of T2*
decay4,5. The acquisition protocol
was optimized in 2 healthy male volunteers (age 30 and 44 years) without USPIO infusion, resulting
in the following parameters: coronal slab orientation, TR/TE = 4.3/0.05ms, flip
angle 15°, FOV 400 mm, matrix 512, 432 spiral interleaves (corresponding to an
undersampling factor of 2) with linear reordering, spiral duration 1160 ms, stack of 256
partitions interpolated to 320, acquisition time 8 minutes. The sequence looped
over partitions and spiral angles in its inner and outer loops, respectively. Patients with prostate cancer scheduled
for USPIO-enhanced MRI as part of their clinical diagnostic workup were
enrolled. Stack-of-spirals UTE was added to the end of their clinical
examination, which also included a 3D T1-weighted GRE sequence and a 3D
T2*-weighted water-selective MEDIC sequence, both at 0.73 mm isotropic
resolution. UTE images were reconstructed offline using the L1-ESPIRiT
implementation of the BART toolbox6, employing manual coil selection to
reduce streaking artifacts originating from structures outside the FOV. Images
were assessed on the presence of signal hyperintensity in LNs, and scored on
image quality, visibility of LNs and blood vessels, and artifacts on 5-point
scales by a radiologist and a physicist in consensus, both with 7 years of
experience in USPIO-enhanced pelvic MRI.Results
After
protocol optimization, four male patients with prostate cancer (age 54-75 years)
were included. One of these had had an intraprostatic injection of
superparamagnetic iron oxide (SPIO) particles 3 weeks prior to USPIO infusion,
and one had surgical clips in the area of interest. Imaging was successful in
all 4 patients. Image quality was rated good to excellent in all patients (Figure 1, Table 1), with excellent and strongly hyperintense depiction of the vasculature
and high SNR. Although the overall visibility of LNs varied between patients,
T1-mediated hyperintensities were observed in at least 1 LN in all patients
(Figure 2). Some variations in contrast behavior in T2*-weighted MEDIC and
T1-weighted UTE were observed between LNs (Figure 2). Artifacts due to
respiratory or bowel motion, streaks, or foldover into the pelvic region were minor
(Figure 3). Blooming artifacts were observed in the patients with
intraprostatic SPIO injection and surgical clips, but not in the other
patients. Chemical shift related artifacts were observed at the borders between
watery and lipid tissues (e.g. between muscle and surrounding lipid tissue,
Figure 3).Discussion
This
work shows that high-resolution T1w USPIO-enhanced MRI of pelvic LNs is
feasible in patients with prostate cancer, and that intranodal T1-mediated
signal enhancement can indeed be observed. The observed variations in contrast
behavior between T2*-weighted and T1-weighted UTE support the hypothesis that
T1w imaging may hold complementary information, but larger studies are needed
to investigate this further. The fat-water artifact observed at the boundary
between muscle and lipid tissue may mimic T1-induced signal enhancement at the
boundary between the watery LNs and surrounding lipid tissue. This may be
mitigated by using fat suppression techniques, or by decreasing the duration of
the spiral readouts. Both would likely lead to an increase in
scanning time; however, the high SNR obtained suggests that further acceleration of the
acquisition may be possible. Golden angle reordering may then be advantageous for
reducing undersampling artifacts.Conclusions
T1-mediated
signal hyperintensities can be observed within pelvic LNs of patients
post-USPIO infusion using a stack-of-spirals UTE sequence, at 0.8mm isotropic
resolution in less than 10 minutes. Although further optimization is warranted,
this opens the possibility of investigating the possible additional value of
T1w UTE imaging for the diagnosis of LN metastases.Acknowledgements
No acknowledgement found.References
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