Masako Ohno1, Tosiaki Miyati2, Naoki Ohno2, Hiroko Kawashima2, Kazuto Kozaka1, Yukihiro Matsuura1, and Toshifumi Gabata1
1Kanazawa University Hospital, Kanazawa, Japan, 2Kanazawa University, Kanazawa, Japan
Synopsis
To
acquire more detailed information on perfusion and diffusion in breast cancer,
we analyzed three diffusion components using triexponential function.
Perfusion-related
diffusion (Dp), fast free
diffusion (Df), and slow
restricted diffusion coefficients (Ds)
were calculated from triexponential function. We compared these parameters between
invasive ductal carcinoma (IDC) and ductal carcinoma in situ (DCIS) groups.
Ds was
significantly lower in the IDC group than those in the DCIS group because
of difference in the cellularity.
Triexponential
analysis makes it possible to noninvasively obtain more detailed information on
perfusion and diffusion in breast cancer, thereby assisting in the diagnosis.INTRODUCTION
Differentiation
of various malignant breast cancer, eg, invasive ductal carcinoma (IDC) and
ductal carcinoma in situ (DCIS), is essential for treatment
and management of breast cancer. Moreover, quantitative evaluation of perfusion and
diffusion information is useful for the diagnosis, monitoring, and treatment
management of breast cancer [1, 2]. Intravoxel incoherent
motion (IVIM) analysis with diffusion-weighted images can provide perfusion and
diffusion information [3]. However, these overlap with each other, and
theoretically there are three diffusion components, ie, perfusion-related
diffusion, fast-free diffusion, and slow-restricted diffusion [4]. Therefore, to
acquire more detailed information on perfusion and diffusion in breast cancer,
we analyzed these three diffusion components using triexponential function.
METHODS
On a 3.0-T MRI,
single-shot diffusion echo planar imaging with multiple b-values of 0 to 3000 s/mm
2
(15 points) was performed in 41 patients with IDC (mean age, 55.8 years; range,
31-85 years) and 7 patients with DCIS (mean age, 52.7 years; range, 41-69
years). The signal intensity at each b-value in the lesion was obtained. Then,
we derived perfusion-related diffusion (
Dp),
fast free diffusion (
Df),
and slow restricted diffusion coefficients (
Ds)
calculated from triexponential function by a two-step approach in which the
literature value of the diffusion coefficient of free water at 37 degrees centigrade (3.0×10
-3
mm
2/s) was assigned to
Df
[5]. In addition, we derived perfusion-related diffusion (
D*) and slow restricted diffusion coefficients (
D) using biexponential analysis to
compare with triexponential analysis. We compared these parameters between the
IDC and DCIS groups.
RESULTS AND DISCUSSION
Ds and
D were
significantly lower in the IDC group than those in the DCIS group (Table 1). These
results can be explained by the fact that the cellularity of IDC was increased
compared with that of DCIS (Figure 1).
Dp
of the IDC showed a tendency to be higher, but not significant, than that of
the DCIS. This result agreed with the previous report which has demonstrated
stronger contrast enhancement in IDC than DCIS because of the higher tumor
angiogenesis in IDC [6]. Moreover, there was no significant correlation between
Dp and
Ds (Table 2), suggesting
that
Dp and
Ds do not necessarily provide
the same kind of information. On the other hand, we found a positive
correlation between
D* and
D. These results indicate that
triexponential analysis could extract independent diffusion information better
than biexponential analysis.
CONCLUSION
Triexponential analysis
makes it possible to noninvasively obtain more detailed information on
perfusion and diffusion in breast cancer, thereby assisting in the diagnosis.
Acknowledgements
No acknowledgement found.References
[1] Shi J, et al. Med Phys 2009;36(11):5052-5063.
[2] Bogner
W, et al. Radiology 2009; 253(2):341-351.
[3] Le Bihan D, et al. Radiology 1988; 168:497–505.
[4] Hayashi T, et
al. J Magn Reson Imaging 2013; 38
(1):148-53.
[5] Ohno N, et al. J Magn Reson
Imaging 2015; in press.
[6] Jansen S A, et al; J Magn Reson
Imaging 2011; 33:1382–1389.