Suhail Parvaze P1, Rakesh K Gupta2, Rupsa Bhattacharjee3, Anup Singh4, Rakesh Kumar Singh5, Gaurav Khanna6, Amal Roy Chaudhary7, Rana Patir8, Sandeep Vaishya8, Jaladhar Neelavalli 9, and Tejas Shah9
1Philips Innovation Campus, Bangalore, India, 2Department of Radiology and Imaging, Fortis Memorial Research Institute, Gurugram, India, 3Indian Institute of Technology Delhi, Delhi, India, 4Department of Biomedical Engineering, Indian Institute of Technology Delhi, Delhi, India, 5Fortis Memorial Research Institute, Gurugram, India, 6SRL Diagnostics, Fortis Memorial Research Institute, Gurugram, India, 7Radiation Oncology, Fortis Memorial Research Institute, Gurugram, India, 8Department of Neurosurgery, Fortis Memorial Research Institute, Gurugram, India, 9BIU, Philips Innovation Campus, Bangalore, India
Synopsis
Edema
in GB is characterized by the presence of tumor cells infiltration as compared
to brain metastasis with only pure edema. Radiomics features extracted using FLAIR
images in GB and BM are found to be exhibiting variation in some of the entropy
and non-uniformity-based features, which could be used as signature to
differentiate GB from brain metastasis.
Introduction
Differentiation of glioblastoma from solitary
brain metastasis (BM) is challenging due to their similar appearance on MRI [1].
Glioblastoma (GB) originates in vivo from the brain parenchyma while metastasis
seeds into the brain parenchyma from rest of the body. Both of these
pathologies usually produce extensive peritumoral edema, central necrosis and
variable hemorrhage. GB shows enhancing and non-enhancing components and tumor
cells are seen with the edema apparent on imaging and have been validated on
histopathology while metastatic lesions are not infiltrative with localized
boundary defined by the post contrast study [2][3][4]. Differentiating
edematous tissue (EDT) from non-enhancing-tumor tissue (NET) and identifying
the clear peritumoral boundaries of EDT are some of the major challenges that are
critical to their differentiation and management [5]. Conventional MRI is not
yet successfully able to delineate EDT, especially in GB. Combination of FLAIR
and DCE-MRI has, to some extent, segmented the EDT and NET tissue [6][7][8].
However, EDT segmented by this approach still demonstrates infiltration of
tumor cells on histopathology. We hypothesize that certain radiomics features
of edema seen in metastasis should be specific to differentiate peritumoral
edema with infiltrating tumor cells from metastasis with no tumor cell
infiltration within edema. Radiomic features of edema from subjects with
meningioma were used as a baseline for understanding EDT having no tumor cell
infiltrationsMethods
In this study 48 surgery naïve histologically
proven GB and 21 BM subjects were evaluated. 6 subjects with meningioma were
also considered for the purpose of characterizing pure edema seen in adjacent
brain parenchyma. Subjects which didn’t have EDT segmented by the perfusion
parameters were excluded in the study. Multimodal image acquisition was
performed on Philips Ingenia 3T scanner with a 15-channel head coil, T1-weighted,
FLAIR, T1-DCE MRI and post contrast T1GD images were acquired. DCE T1-perfusion
MRI data analysis was carried using in-house code to generate perfusion parameters
and kinetic parameters [8]. Respective demographics such as age span (AS) and
male to female ratio (MFR) of the subjects are as follows; for meningioma AS (34-72
years), MFR (4:2), BM - AS (33-70 years), MFR (14:7) and GB - AS (34-71), MFR
(30:18). The distribution pertaining to origin of BM from various cancers are
as follows, lung carcinoma -12, breast -5, gastroenterology - 1, endometrial -2
and pancreatic -1. T1 perfusion parameters (CBF, rCBV etc.,) were computed which
were used to generate tissue specific segmentation masks with the aid of SVM
classifier [8]. Tumor sub-regions namely contrast enhancing tumor (ET) and necrosis
(NEC) were delineated using post contrast (T1GD) sequence. Whereas, NET and EDT
were delineated using FLAIR images and trained SVM model [8]. Subsequently, a 2D
binary mask was extracted from the normal appearing white matter (NAWM) region on
FLAIR image. Radiomics based feature extraction was implemented using
PyRadiomics 2.2.0 library [8]. Radiomics
features were extracted from the EDT ROI for subjects belonging to GB, BM and
meningioma using FLAIR images. Same texture features were also extracted from
the NAWM [9]. Statistical significance was computed for Radiomics features from
EDT extracted between BM and meningioma and also computed for features between
GB and BM – meningioma combined as one group [10]. The pipeline of the work
implemented in this study is demonstrated in Figure 1Results
The input sequences and feature maps of
representative images are shown in Figure 2. Comparison of Radiomics features
across GB, BM - meningioma resulted in 14 significant features (Table 1).
Radiomics features were statistically insignificant in the EDT regions between
meningioma and BM and hence were combined as one group for its differentiation
from GB edema. Radiomics features from EDT representing GB had higher values
than BM and meningioma except for one feature. The representative feature map
of one of the significant feature GLRM-Run length non-uniformity (GLRLM-RLNU)
is depicted in the Figure 2Discussion
Results in this study indicate that Radiomics
features were able to differentiate the texture variation across NAWM and EDT
in GB, BM and meningioma. EDT features in BM and meningioma found to be
insignificant. This might be due to the fact that there exists commonality in EDT
across these two tumor types. Some of Radiomics features were significant to
differentiate the EDT of GB from BM. This further substantiate that the EDT in GB
has infiltrating tumor cells and differ from peritumoral edema seen in BM. Most
of the significant features belonged to either entropy or non-uniformity
categories. High entropy and non-uniformity in the GB features also may be
aiding in the understanding of EDT in the GB which is known to contain tumor
cells as compared to BM which is devoid of tumor cell infiltration in the
perilesional edema. The histogram of the feature map obtained using EDT ROI
indicates that the GB has feature values spread whereas in the case of BM the
feature values seems to be skewed. These specific texture features may be of
value in differentiating GB from solitary BM based on the edema features by
demonstrating infiltration in GBAcknowledgements
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