Mehrdad Pourfathi1, Luis Loza1, Stephen Kadlecek1, Ian Duncan1, Diane Lim2, Shampa Chatterjee3, Kai Ruppert1, Sarmad Siddiqui1, Harrilla Profka1, Yan Liu2, Jessica Kim2, Hooman Hamedani1, Yi Xin1, Faraz Amzajerdian1, Maurizio Cereda4, Ryan Baron1, Mary Spencer1, Tahmina Achekzai1, Jose Conejo-Garcia5, and Rahim R. Rizi1
1Radiology, University of Pennsylvania, Philadelphia, PA, United States, 2Sleep Medicine, University of Pennsylvania, Philadelphia, PA, United States, 3Physiology, University of Pennsylvania, Philadelphia, PA, United States, 4Anesthesiology and Critical Care, University of Pennsylvania, Philadelphia, PA, United States, 5Moffitt Cancer Center, Tampa, FL, United States
Synopsis
We demonstrate the feasibility of hyperpolarized MRI technology to image lung cancer in mice. We demonstrated the use of 13C MRSI to detect elevated pyruvate to lactate conversion in the tumor relative to the adjacent non-cancerous lung tissue. We also showed the feasibility of 129Xe imaging to detect non-aerated regions in the lung tissue co-localized with the tumor. The utility of these modalities combined may provide a multi-faceted tool to assess tumor's stage and its response to therapy in lung cancer.
Introduction
CT
and PET/CT are the most commonly-used imaging techniques for lung cancer
screening (1). However, repeated scans for staging and monitoring
tumor response to treatment expose patients to hazardous ionizing radiation. Hyperpolarized
MRI is a set of novel imaging methods that have been used safely in humans: 13C MRI to monitor treatment in
prostate cancer (2), and 129Xe to
characterize altered lung structure and function in a variety of conditions. In
this study, we demonstrate the utility of both techniques for detecting changes
in tumor metabolism and lung function, respectively, in a murine lung cancer
model.Materials and Methods
Tumor was induced in C57BL/6 mice
as previously described (3). Mice were scanned in a 9.4T vertical-bore
micro-imaging MRI system (Bruker Inc.) using either a dual-tuned 1H/13C
or 1H/129Xe resonator (Bruker Inc.). T2-weighted
images were acquired using a dual-echo respiratory gated RARE pulse sequence
(TR/TE1/TE2 = 570ms, 2.1ms, 10.2ms, ETL = 4, NA = 8,
matrix size = 192x192, FOV = 30x30 mm2, 0.8mm slice thickness, 16
slices. For carbon experiments, 22μL of [1-13C]
pyruvate was hyperpolarized using a HyperSense DNP polarizer (Oxford
Instruments HyperSense) and melted rapidly at 180oC to yield a neutral
isotonic solution of 80mM hyperpolarized pyruvate. 200μL of the solution was injected via the tail vein
within 3 seconds. Data acquisition started 10 seconds after the start of
injection, using an 2D FID-CSI pulse sequence (TR/TE = 28/0.5ms, spectral
bandwidth = 6kHz, FA = 9o, matrix size=16x16, FOV = 25x25cm2,
5mm slice thickness). For 129Xe
experiments, enriched 129Xe gas was hyperpolarized via optical
pumping (XeMed XeBox). Xenon Images were acquired using a respiratory-gated coronal
multi-slice FLASH pulse sequence (TR/TE = 100/0.8ms, FA = 60o, matrix
size = 64x64, FOV = 35x25 mm2, 2.5mm slice thickness, 4 slices) while
the mouse was freely breathing a mixture of hyperpolarized 129Xe (30%),
oxygen (20%) and nitrogen (50%).Results and Discussion
Figure 1 shows the T2-weighted image, 13C spectroscopic image and
corresponding pyruvate and lactate maps overlaid on the T2 scan acquired
from a single mouse, three weeks after the induction of cancer in the left lung.
Enhanced lactate signal is co-localized with the tumors (white arrows) in two
locations: over the primary tumor in the lung, as well as the secondary tumor
protruding out of the thoracic cavity. The right panel shows the spectrum
averaged over the healthy lung tissue (voxel A), primary lung cancer in the
lung (voxel B) and a secondary tumor (voxel C). The lactate-to-pyruvate ratio derived
from these spectra is elevated in the tumor (0.82 for the primary, 2.63 for the
secondary tumors) relative to the adjacent normal lung tissue (Lac/Pyr = 0.32).
This suggests that hyperpolarized carbon-13 MRI has the capacity to metabolically
differentiate the tumor from the neighboring non-cancerous lung tissue. Figure
2 shows the T2-weighted scan in another mouse two weeks after
induction of cancer in the left lung. The hyperpolarized 129Xe gas image shows the absence
of ventilation in an area co-localized with the tumor. Further study is
needed to characterize cancer-related changes in lung function and gas uptake
by measuring the dissolved phase of 129Xe around the tumor. While this
data is only preliminary, it nevertheless suggests the feasibility of using both
techniques in combination as a multimodality approach to studying lung cancer.
The advantage of these techniques in a clinical setting is the absence of
ionizing radiation, which makes repeated scanning of patients possible. Conclusions
In this
study, we demonstrated the feasibility of using hyperpolarized 13C and
129Xe imaging to investigate tumor glycolysis and altered lung
function in a murine cancer model, and showed that both techniques have the
ability to detect small tumors. In future studies, we intend to investigate the
utility of both techniques as a multi-parametric approach for obtaining information
about both lung function around the tumor and metabolism in the tumor, with the aim of improving staging and treatment
response monitoring.Acknowledgements
No acknowledgement found.References
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JD et al, JNM2017;58:399–405.
2. Aggarwal
R et al European Urology 2017
3. Sheen
MR et al, Open Life Sciences 10:85