Yoshiyuki Watanabe1, Masahiro Fujiwara2, Takuya Fujiwara2, Hiroto Takahashi2, Chisato Matsuo2, Hisashi Tanaka2, Hideyuki Arita3, Manabu Kinoshita3, Naoyuki Kagawa3, and Noriyuki Tomiyama2
1Future Diagnostic Radiology, Osaka University, Suita, Osaka, Japan, 2Radiology, Osaka University, Suita, Japan, 3Neurosurgery, Osaka University, Suita, Japan
Synopsis
We retrospectively studied 33 consecutive
patients with a diagnosis of GBM or PCNSL performed both DCE and DSC imaging.
The rCBV of GBM are significantly larger,
and Ktrans of GBM was significantly lower than that of PCNSL in CE ROIs. There
was no significant difference between two tumors in CE ROI about other DCE
parameters, Ve, Vp Kep and surrounding ROIS. The ROC analysis performed with
respect to the GBM and PCNSL groups revealed that 90% tile rCBV and 50% tile of
Ktrans showed the largest area under the curve (AUC) of 0.949 and 0.815,
respectively.
PCNSL can be
differentiated from GBM with rCBV value and Ktrans. rCBV was superior to Ktrans
in differentiating two tumors and Ktrans had no additional value in differentiating
these tumors.
Background and Purpose
MRI features of primary central nervous system lymphoma (PCNSL) and
glioblastoma (GBM) are highly variable and sometimes similar complicating
differentiation solely by conventional MRI[1, 2]. In order to provide surgical plans and optimal
treatments for GBM and PCNSL, preoperative differential diagnosis is quite
important. Many previous studies have
aimed to differentiate GBM from PCNSL using advanced imaging, such as
diffusion-weighted imaging (DWI), perfusion MRI and texture analysis, etc. Two
perfusion parameters, dynamic susceptibility contrast (DSC) and dynamic
contrast-enhanced (DCE) –MRI, were reported separately, so there were few
reports to compare DSC and DCE with one examination. The purpose of this study
was to explore the potential use of the DSC and DCE -PWI to differentiate PCNSL
and GBM.
Methods
We retrospectively studied 33 consecutive patients with a diagnosis of
GBM or PCNSL performed both DSC and DCE imaging between 2014 and 2018. All patients had an
untreated enhanced tumor and undergone routine brain MRI, DCE and DSC PWI
before surgical resection. Patients consisted of 20 Glioblastoma (male 16,
female 4, mean age= 57 yr.: 24-83yr) and 13 PCNSL (male 9, female 4, average age=69
yr.: 44-83yr). Two GBM cases and one PCNSL case were excluded due to massive
hemorrhage or artifact from oral metals. MR was performed 3T scanner as
following sequences; Precontrast sequence: T1WI, T2WI, DWI, and FLAIR, DCE
imaging: 0.1ml/Kg Gd-DOTA 3ml/s with saline flash, 3D-SPGR: TR/TE=3.3/1.5ms,
FA=14°,Matrix 192X192, FOV 256mm, slice thickness 7mm X 20 slice , DSC imaging:
0.1 ml/kg Gd-DOTA 3ml/s, GRE-EPI: TR/TE = 2000/21 ms, FA = 60°, matrix 96×128,
FOV 220 mm, slice thickness = 5 mm, 20 slices 1 mm gap and post contrast 3D-T1WI.
Image analysis was performed by Olea
Sphere 3.0 (Olea Medical), DCE analysis by extended Toft model, and DSC
analysis: by Bayesian model. Slice fusion for FLAIR, CE-T1WI, DCE image, DSC
image was performed and two ROI was set in contrast enhanced (CE) area and
surrounding T2 prolonged area. Histogram analysis of each two ROIs was
performed and calculated the Mean, SD, 50%, 90%, 100% tile values. An unpaired
t-test was used to compare the difference in each histogram parameter between GBM
and PCNSL.
The receiver operating characteristic (ROC) curve analyses were
performed to determine optimum thresholds and diagnostic accuracy.Results
The rCBV of GBM are significantly larger,
and Ktrans of GBM was significantly lower than that of PCNSL in CE ROIs (Table).
There was no significant difference between two tumors in CE ROI about the other
DCE parameters, Ve, Vp Kep and surrounding ROISs. The ROC analysis performed
with respect to the GBM and PCNSL groups revealed that the 90% tile rCBV and
50% tile of Ktrans showed the largest area under the curve (AUC) of 0.949 and
0.815, respectively.
Figure shows the scatter plots of the 90%
tile rCBV and 50% tile Ktrans. rCBV showed good performance in differentiating GBM
and ML, and Ktrans had no additional information to distinguish the two tumors.Discussion
There are many
previous reports about rCBV or DCE parameters differentiating GBM from PCNSL [3-8], and rCBV has a propensity to show large AUC values.
However, there were only few reports about combining these two methods. DSC and
DCE are different parameters of tumor perfusion and permeability. In terms of
malignant tumor differentiation between GBM and ML, DCE was of low importance.
Conclusions
PCNSL
can be differentiated from GBM with rCBV value and Ktrans. rCBV was superior to
Ktrans in differentiation two tumors and Ktrans had no additive value to
differentiate these tumors.Acknowledgements
NoneReferences
1. Koeller,
K.K., J.G. Smirniotopoulos, and R.V. Jones, Primary
central nervous system lymphoma: radiologic-pathologic correlation.
Radiographics, 1997. 17(6): p.
1497-526.
2. Rees, J.H., et al., Glioblastoma multiforme:
radiologic-pathologic correlation. Radiographics, 1996. 16(6): p. 1413-38; quiz 1462-3.
3. Lu, S., et al., Utility of dynamic contrast-enhanced magnetic resonance imaging for
differentiating glioblastoma, primary central nervous system lymphoma and brain
metastatic tumor. Eur J Radiol, 2016. 85(10):
p. 1722-1727.
4. Kickingereder, P., et al., Evaluation of microvascular permeability
with dynamic contrast-enhanced MRI for the differentiation of primary CNS
lymphoma and glioblastoma: radiologic-pathologic correlation. AJNR Am J
Neuroradiol, 2014. 35(8): p. 1503-8.
5. Murayama, K., et al., Differentiating between Central Nervous
System Lymphoma and High-grade Glioma Using Dynamic Susceptibility Contrast and
Dynamic Contrast-enhanced MR Imaging with Histogram Analysis. Magn Reson
Med Sci, 2017.
6. Nakajima, S., et al., Differentiation between primary central
nervous system lymphoma and glioblastoma: a comparative study of parameters
derived from dynamic susceptibility contrast-enhanced perfusion-weighted MRI.
Clin Radiol, 2015. 70(12): p.
1393-9.
7. Toh, C.H., et al., Differentiation of primary central nervous system lymphomas and
glioblastomas: comparisons of diagnostic performance of dynamic susceptibility
contrast-enhanced perfusion MR imaging without and with contrast-leakage
correction. AJNR Am J Neuroradiol, 2013. 34(6): p. 1145-9.
8. Ma, J.H., et al., Differentiation among glioblastoma multiforme, solitary metastatic
tumor, and lymphoma using whole-tumor histogram analysis of the normalized
cerebral blood volume in enhancing and perienhancing lesions. AJNR Am J
Neuroradiol, 2010. 31(9): p.
1699-706.