Synopsis
In DCE-MRI, T1 map is necessary for signal to concentration
conversion. In highly fat-water mixed tissue such as breast, contrast uptake
primarily changes T1 values of water protons. Therefore, DCE quantification in
breast cancer must reliably measure water T1. We evaluated T1 maps
obtained using Dixon based fat-water separated VFA method and compared values
in fat, fibro-glandular tissue and tumors. We observed that T1 mapping with Dixon
based VFA method and non-linear fitting recovers T1 values for
tissue in breast by reducing partial volume. We conclude that water only T1
mapping will improve accuracy of PK modeling in breast cancer.Purpose
In
breast tumor characterization, DCE-MRI is commonly used for understanding the
vasculature changes associated with neo-angiogenesis [1]. For
DCE-MRI, pre-contrast T
1-relaxation mapping is necessary for
converting signal to contrast concentration for pharmaco-kinetic (PK) modeling. However, contrast uptake primarily affects T
1 relaxation rate
of water protons only, and not fat protons [2]. Hence, in breast tissue with a high
density of fat and water mixed voxels, generating water-only T
1
relaxation maps is necessary for accurate PK modeling [3,4,5]. In this study, we
evaluated T
1 relaxation maps obtained using traditional
non-fat-suppressed variable flip angle (VFA) data with those obtained from
Dixon based fat-water separation VFA method. Results are presented in fat, fibro-glandular
tissue (FGT) and breast tumors.
Methods
Patient
database: Six breast cancer patients were scanned on a GE 3T MR750 scanner using an
8-channel breast coil. An appropriate IRB approved all the studies. Imaging: T
1 mapping consisted
of two different acquisitions:
a. Conventional
3D SPGR non-fat suppressed variable flip angle (
T1-VFA) method: TE/TR =
2.1/5.28 ms, five FA= (2, 3, 5, 10, 15)º, matrix size=256×256×112 (1.36mm×1.36mm×1.4mm resolution), axial
orientation;
b. VIBRANT-FLEX-VFA : Dixon
based method to generate fat-only and water-only images with TE/TR = 1.2, 2.3 /
5.3 ms, and flip angles and geometry as described in a
above. Fat-only images were available in four cases, while water-only and conventional
(T1-VFA) images were available in all six patients.
c.
Bloch-Siegert [6] based B
1
map acquisition using a body receive coil with 2D-GRE and TE/TR =
13.5/30ms, FA = 20º, matrix
size=128×128×22 (2.73mm×2.73mm×7mm resolution). Fat fraction was computed using FA = 2º fat and water images.
T1 mapping: An
in-house tool developed within the Insight Toolkit (ITK) framework was used for
VFA based T
1 mapping [7]. Bloch-Siegert
based B
1 data was processed to obtain spatially varying scaling
factor for FA correction. No significant geometrical distortions were observed
between B
1 data and VFA data and hence only an identity transform
was used for geometric matching of B
1 map to T
1 data. The
flip angle corrected VFA data were processed to obtain T
1 map using:
linear fitting and non-linear Levenberg–Marquardt fitting. To assess goodness-of-fit
for T
1 mapping, coefficient of
determination (R
2) was computed.
Analysis: A trained radiologist marked representative ROIs
in both left and right breast for fat (on fat-only, 2º,N=4), FGT (water-only,
15º, N=6)
and tumor lesion (water-only, 15º, N=2). Only
those voxels with R
2 > 0.5 for T
1 model fit were retained.
Results and Discussions
Figure
1 demonstrates well-known variation of transmit B
1 in breast imaging
at 3T (left breast scaling ~= 1.2, right breast scaling ~= 0.8) [8]. Fat T
1
values from fat-only images are lower (337±50 ms) compared to those with T1-VFA
(442±35 ms) (Figure 2) and match with literature values [4,9]. For FGT, T,
1
values were elevated with water–only images (1489±265 ms), compared to T1-VFA
images (1238±138 ms) and similar to previous literature values for FGT (1444ms)
[3,9]. R
2 values for water-only images were lower (~0.82±0.08),
compared to T1-VFA based images (~0.9±0.06) (Figure 3). For tumor
lesions (Figure 4, A and B), in one case where fitting accuracy was higher (R
2
= 0.82), there was a 10% increase in T
1 with water-only (2780 ms)
compared to T1-VFA (2523 ms). However, in other tumor case, with relatively
poor fitting (R
2 = 0.77), we noticed reduction (26%) in the T
1
value with water-only (1638 ms), compared to T
1-VFA (2216 ms). Further
investigation indicated that motion across FA volumes was responsible for this
apparent reduction in T
1 values (Figure 4C). Lesion mask was drawn on
FA =15º water-only image, while other FA images had moved from this
reference. As a result, the fat-voxels (fat fraction in lesion = 0.29±0.3) from
surrounding region (patient had very fatty breast) were counted in tumor ROI
and reduced the tumor T
1 (See Fig 4C). Matching FA = 15º to FA = 2º using dense
registration and warping tumor mask accordingly increased T
1 value
for tumor to 2038 ms. With water-only images and in FGT and tumor regions, non-linear
fitting produced slightly elevated T
1 values compared to linear
fitting (Fig 5A), as well as marginally higher R
2 with non-linear (0.8)
compared to linear fitting (0.78, p < 0.01) (Fig 5B). Bland-Altman analysis indicated
a mean bias of 17 ms (limits of agreement = +84 to -118 ms) (Fig 5C).
Conclusion
We
demonstrate that T
1 mapping with Dixon based VFA method and non-linear
fitting recovers the T
1 values for tissue in breast by reducing partial
volume effects. The Dixon water only T
1 mapping will improve the accuracy
of PK modeling in breast tumors.
Acknowledgements
No acknowledgement found.References
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