Virendra Kumar Yadav1, Neha Vats1, Manish Awasthi1, Dinil Sasi1, Mamta Gupta2, Rakesh Kumar Gupta2, Sumeet Agarwal3, and Anup Singh1,4
1Center for Biomedical Engineering, Indian Institute of Technology, Delhi, India, 2Fortis Memorial Research Institute, Gurugram, India, 3Electrical Engineering, Indian Institute of Technology, Delhi, India, 4Biomedical Engineering, AIIMS, New Delhi, India
Synopsis
Segmentation of brain tumor lesion is important
for diagnosis and treatment planning. Tumor
tissue and edema usually appears hyperintense on fluid-attenuated-inversion-recovery (FLAIR) MR images. FLAIR images are widely used for brain tumor localization
and segmentation purpose. In this
study, a Support-Vector-Machine
(SVM) model was developed for segmentation of FLAIR hyper-intense region semi-automatically
using BraTS 2018 dataset. The proposed approach require a minimal user
involvement in selecting one region around tumor in the central slice. It was
observed that proposed SVM approach segmentation results shows better dice
coefficient in comparison to what reported in literature.
Introduction
Accurate
detection and segmentation of brain tumors in MRI images assists in treatment
planning. Increasing amount of brain imaging data has made the clinical expert
job tiresome1. To reduce the manual effort in accurate diagnosis by
the clinician and speedup the process, several alternative ways has been
investigated1-8. Various semi-automated and fully automated process have
been proposed in literature to carryout tumor segmentation task using MRI
images1-8. In clinical practice, semi-automatic approaches are
adopted2. Advantage of semi-automatic approach is, radiologist
control over segmentation process to ensure accuracy2. This study
aims to develop a machine learning (i.e. support vector machine) based
semi-automatic system to carry out the tumor segmentation task from 3D
Fluid-attenuated inversion recovery (FLAIR) MR images of brain.Method
A total
60 FLAIR images (30 images from LGG and 30 images from HGG) were chosen from
BraTS dataset for development and testing of SVM model9-11. Intensity value of each voxel of FLAIR images is
only considered feature. For training SVM Model, a rough Region of
Interest (ROI) of any shape (square, polygon, circle etc.) is selected on FLAIR
image which contains tumor. All futher computation was performed on this
selected ROI instead on whole FLAIR image. Intensity scaling (0-255) was
performed. Let’s represent this ROI mask as R1mask (Figure
1). Segmented tumor masks are also available in BraTS 2018 dataset, which
serve as ground-truth for training and validation. Let’s represent this
ground-truth mask, over same ROI, as R2mask(Figure 1). Multiply R1mask with R2mask
provided hyperintense region of FLAIR image and let’s represent it by R3.
Subtract R3 from R1mask to obtain Rsub.
From Rsub a data set V1- is created for non-zeros intensity values containing
two column vectors: intensity value and label (figure 1). Put all labels ‘-1’
in label field of data set V1- . Similarly generate a
data set V1+ of similar structure from R3. Put
all labels ‘1’ in label field of vector V1+ . This
process is carried out for 20 FLAIR images (10 images from each HGG and LGG
respectively) containing tumor region. Finally, a combined dataset V is created
containing all intensities along with their corresponding labels i.e. 1 or -1. Every
voxel intensity along with their corresponding labels was considered as sample.
Dataset was divided into training set and testing set in 90:10 ratio. Ten-fold
cross validation was used to validate proposed SVM model. SVM model was trained
using linear kernel. A range of C (0.0001-1000) in SVM model was investigated
to obtain the value of C for which mean of Ten-fold cross validation error was minimum.
Observed C value for which model produce minimum Ten-fold cross validation
error was accepted to develop the final model for FLAIR hyperintense lesion
segmentation. To use this final developed model, a user has to visually scan
the FLAIR images of a particular patient in search of images containing tumor.
A FLAIR image which contain tumor of larger size compared to other tumor slices
is chosen and around tumor, a rough ROI is drawn on this chosen FLAIR image and
applied to all surrounding slices automatically. From these ROIs, proposed SVM
model will result tumor segmentation for all FLAIR images which contains tumor.
For testing accuracy of segmentation, dice coefficient index was computed
between proposed segmentation based mask and available groundtruth mask from
data of new test patients. Result
Observed
error percentage in training, validation and testing set were 8.5973,
8.594 and 8.597 respectively for best C (equal to 1). Developed SVM model, tested
against 40 images (HGG=20, LGG=20) taken from BraTS 2018 dataset provided an average
dice score against ground truth (available in BraTS 2018 dataset), equal to 87.7
and 86. 8 for HGG and LGG images respectively (Table I). Proposed model resulted
better segmentation accuracy compared to previously reported results available
in literature (Table II).Discussion
Advantage
of using BraTS 2018 dataset is that it contains image sequences which were
collected worldwide by using different clinical image acquisition protocol,
different scanners and from multiple organizations. It is believe that Training
SVM model on such a dataset generalizes SVM model. A manual ROI is selected
around specific region of interest (around tumor) of any shape. Selecting rough ROI (around tumor) did not requires much expertise and skills. As all the
processing is performed on selected ROI on FLAIR image instead on whole image,
resulted in reduced computation time. Voxel intensity is only considered feature in training
SVM model at this stage for classifying pixel as tumor or non-tumor pixel. Proposed
approach not only exploits the advantage of semi-automatic approaches but also
take care interobserver variability in segmentation process.Conclusion
In
this study, an effort has been made to develop a semi-automatic model (SVM
based) to segment hyperintense lesion in FLAIR images for clinical use. The
proposed model uses single imaging sequence (FLAIR), an ROI which is smaller in
size as compared to the original image and one feature i.e. voxel intensity,
which makes it relatively fast. It was found that developed SVM model when tested
against some other images which were not included in the training (from BraTS
2018 dataset) showed improved performance compared to other approach’s results
reported in literature.Acknowledgements
This work was supported by Indian Institute of Technology Delhi and Fortis Memorial Research Institute Gurugram. The authors thanks Dr. Anirban Sengupta, Dr. Ayan, Rafeek, Esha, Dharmesh, Umang and Dr. Sumantra Dutta Roy for their valuable suggestion. References
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