Abstract:
Compelling clinical studies have shown that lung cancer screening allows for early
diagnosis and treatment of lung cancer. Despite the high quality CT images available
to the radiologists for decision making, missing lung cancer on the chest radiograph
attributes to errors made by the radiologists in determining whether a lung nodule is
malignant or not, on the basis of medical imaging and other clinical information.
Several research studies have recommended Computer Aided Diagnosis (CADx)
systems which facilitate early detection of lung cancer nodules at more curable stages.
The significant and on-going research areas in CADx systems include automated
segmentation systems and classification models for nodules characterization. The non
availability of large databases has been a limitation for the training and development of
accurate diagnostic models.
The thesis aims to develop image analysis based methods in 3-D to improve the
performance of CAD systems for lung cancer detection and pathological stage
estimation. The contributed research work was carried out in the areas ol segmentation
and cancer diagnostic models respectively which are integral parts of a CAD system.
During the first phase of research, a semi-automatic 3-D segmentation algorithm
developed for varying nodules sizes and shapes which enables accurate volumetric
assessment and further analysis for nodules characterization in Computed Tomography
(CT) images. The proposed model performs nodule segmentation by incorporating the
geometric and region based properties of a lung nodule in CT images. An adaptive
approach was developed to compute the mean gray level intensity of a lung nodule
which is used as a stopping function besides the gradient properties to enable accurate
nodule extraction from the CT images. The algorithm was tested and validated on
multiple databases including LIDC, FDA, RIDER and CUMC with a mean spatial
was
overlap of 85% As second research contribution, a Bayesian Inversion framework was devised
to predict the cancer occurrence as well as its pathological stage. The proposed
stochastic model was tested on NLST database, a repository of low dose longitudinal
CT data sets and is aimed to address the constraint of limited number of annotated CT
datasets in lung cancer for multi-class classification. To develop the proposed
framework, quantitative imaging features known as radiomic features were extracted
from the segmented nodules (benign and malignant), analyzed and ranked using an
intuitive approach to identify the diagnostic features for cancer and its stage estimation
respectively. The carried out research work showed that Surface Area and Sum Entropy
are the two radiomic features that possess general phenotype/characteristics to
differentiate between benign and cancerous tumors of lung, colon and head and neck
cancer respectively. These highly discriminating features were validated by integration
into non-linear mathematical equation and achieved an accuracy of 97.0% for lung
nodule classification.
Another group of radiomic features was investigated in malignant nodules
which can differentiate between early stage (stage I and stage II) and advanced stage
(stage III and stage IV) cancer. Based on the analysis performed using regularization
method and supervised feature selection, radiomic features which showed strong
discrimination between early and advanced stage cancer were Sphericity, Large
Dependence High Gray Level Emphasis (LDHGLE), Cluster Prominence, Small Area
Emphasis and Strength respectively. These features were integrated into a mathematical
equation for validation and achieved an accuracy of 86.84% when tested on data sets
of malignant nodules with early and advanced stage cancer.
By incorporating the aforementioned formulated equations for cancer and its
stage detection respectively, the proposed stochastic framework predicted the
occurrence as well as its pathological stage with an accuracy of 86%