Towards survival prediction of cancer patients using medical images

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PeerJ Computer Science

Introduction

Medical imaging has been a highly adopted technique for diagnostics in the healthcare sector due to its speed, accuracy, and non-invasiveness. According to the National Health Service (NHS), in 2020, 40.4 million medical imaging tests are performed in United Kingdom (England & Improvement, 2016). Similarly, the global market size of medical imaging is estimated to be $26 billion in 2021 with expected growth to $35 billion by 2026 (Markets, 2021). This adaption of different medical imaging modalities like positron emission tomography (PET) (Bailey et al., 2005), magnetic resonance imaging (MRI) (Lam, 2018), and computed tomography (CT) scan (De Chiffre et al., 2014) by doctors is attributed to their aid in better diagnosis, treatment, and prognosis. In general, these medical images are used to diagnose heart disease, lung disease, Coronavirus disease 2019 (COVID-19), fractured bones, cancer, and brain disorders (Sharma & Aggarwal, 2010). Moreover, Artificial Intelligence (AI) based computer-aided diagnosis (CADx) algorithms are providing additional advantage of automatically identifying and interpreting the anomalies from images to assist doctors in clinical diagnostics and prognosis. One key aspect of such clinical prognosis is survival prediction of patients using information like age, sex, disease history, and profile. In this regard, researchers have developed different scoring techniques like thrombolysis in myocardial infarction (TIMI) risk (Antman et al., 2000), Global Registry of Acute Coronary Events (GRACE) (Tang, Wong & Herbison, 2007), NSTEMI (non-ST-segment elevation myocardial infarction), Pitt bacteremia Score (PBS) (Henderson et al., 2020; Marchesini, Morelli & Piangerelli, 2015), and acute physiology and chronic health evaluation II (APACHE II) (Park et al., 2009) to predict the survival time of patients. These scoring methods are designed after experimenting and selecting the most important factors contributing to the survival of the patient (Widera et al., 2012). In addition to clinical information, medical images also provide a novel opportunity to predict the survival rate of cancer patients after examining the complex visual features of tumorous cells. In general, different types of radiomic and hand-crafted features of the image are extracted to examine the relationship between visual features and survival rate of patient (Banerjee, Mitra & Shankar, 2018; Alam et al., 2018). For instance, shape-based and first-order based radiomic features are used for survival prediction of brain tumor patients form BraTS dataset (Sun & Zhang, 2018; Banerjee, Mitra & Shankar, 2018). Similarly, hand-crafted features of tumor like volume, volume ratio, and position, etc., of tumor cells are introduced for survival prediction (Guo et al., 2019; Banerjee, Mitra & Shankar, 2018). However, these studies are limited to specific pre-selected feature types and machine learning models. It’s inevitable that someone will do a major review of different features, feature selection methods, and machine learning models.

In this article, we test the performance of 10 machine learning models with gold standard BraTS and NSCLC datasets containing brain tumor and lung cancer images, respectively. Also, we extract and compare the performance of nine classes of radiomic and hand-crafted features of medical images. Precisely, we evaluate a total of 540 combinations formulated by using eight feature classes, six feature selection methods, and 10 machine learning models. For classification, we find that Logistic Regression (LoR) outperforms competing models on MRI and CT scanned images. LoR model gives the maximum 66% and 54% accuracy on BraTS and NSCLC datasets, respectively. Similarly, the Linear Regression (LR) model is the best performing model for regression with 52–53% accuracy on both datasets. Moreover, age is the most important factor in the survival prediction of cancer patients. Our major contributions and findings are as follows:

  • We evaluate the performance of 156 image features from nine classes, six feature selection methods, and 10 machine learning models to select the best performing model and features for MRI and CT scanned datasets of BraTS and NSCLC, respectively.

  • A comprehensive analysis using the AUC score for each model shows that logistic regression is the best performing classifier and more ‘stable’ model with 0.769 and 0.751 AUC score for BraTS and NSCLC, respectively.

  • Our analysis on features highlights that shape-based and gray level contrast features are best performing features for MRI scanned data. While grey level symmetry features perform best for CT scanned images.

  • Experiments and analysis show that logistic regression and linear regression models are more suitable models for survival prediction purposes as compared to decision tree, multilayer perceptron, artificial neural network, random forest, and support vector machine models.

The rest of the article is structured as follows: we explain the literature review in ‘Literature review’. Next, the details of the datasets are presented in ‘Dataset’. In ‘Methodology’, the proposed methodology to understand the medical images is detailed while the results and findings are explained in ‘Results’. Finally, we conclude our article in ‘Conclusion’.

Literature review

In recent years, the research community has worked effectively on examining the medical images for survival prediction of patients (Kickingereder et al., 2016). For instance, Baid et al. (2018) and Baid et al. (2020) experimented with radiomic features of first-order statistics, shape-based 2D, shape-based 3D, gray level run length matrix (GLRLM), and GLCM using multilayer perceptron (MLP) and random forest models for survival prediction of brain tumor patients (Baid et al., 2018; Baid et al., 2020). Similarly, a study evaluated the performance of first-order statistics, GLCM, and neighbouring gray tone difference matric (NGTDM) along with age by applying a recursive feature selection method to select best performing features (Alam et al., 2018). Using the Extreme Gradient Boosting model, authors reported the age as most important feature for survival prediction. In addition, radiomic features like volumetric, textural, and shape-based were tested for survival prediction task of BraTS datasets (Baid et al., 2020). In a similar vein, pre-trained neural network model of the Visual Geometry Group (VGG16) was augmented with volumetric and age features for survival prediction of patient (Cabezas et al., 2018). Moreover, hand-crafted features such as tumor volume, volume ratio, surface area, the position of the enhancing tumor etc. have shown significant results for survival prediction of patients (Guo et al., 2019).

Selection of important features reducing the complexity and redundancy of features enhances the performance of machine learning models. In this regard, Gates et al. (2018) applied step-wise, univariate, and multivariate feature selection methods for selection of best radiomic features. Their analysis highlighted that gray level run length matrices (GLRLM) and NGTDM were not important features for patient survival prediction of brain tumor patients. In addition, the SVM model was also applied along with recursive feature elimination with cross-validation (RFECV). Moreover, location-based features of tumorous areas were tested for survival prediction (Soltani et al., 2021). In the study, authors compared the performance of LR, Support Vector Regression (SVR), and random forest (RF) regression models and concluded that tumor location-based features significantly impacted the performance of survival prediction task. Finally, the neuromorphic convolution neural network was also designed for survival prediction for brain tumor patients (Han & Han, 2018). Also, the performance of all radiomic features with feature selection methods of RFE, univariate feature selection, and SelectFromModel (Scikit-learn developers, 2021b) was evaluated. In a similar study (Sun & Zhang, 2018), authors extracted radiomic features and applied least absolute shrinkage and selection operator (LASSO) (Tibshirani, 1996) methods for selection of top features. In addition, researchers applied step-wise forward and backward selection methods for the selection of the top features (Hoerl & Kennard, 1970). For the experiment, MLP, RF, and support vector regression models were applied for predicting the survival days.

The survival prediction of lung cancer patients using CT scanned images and radiomic features is a well-explored area of research. Authors extracted radiomic and automatic features from CT scanned images using the ResNet18 network and used a CNN for the lung cancer patient survival time prediction (Ayyachamy et al., 2019). In addition, the binary classification (dead or alive) was done by utilizing radiomic features from CT scan features, clinical information, and ANN model (Chufal et al., 2019). The comparative analysis of the Bayesian network and SVM was also conducted for the survival prediction of patients (Jayasurya et al., 2010). The comparison highlighted the better performance of the Bayesian network with noisy data. Additionally, a study focusing on shape-based, intensity, and texture features of CT scanned images achieved the best performance (confidence interval 0.62−0.74) with gradient boosting linear model (Sun et al., 2018).

Table 1 shows the comparison of our work with the literature review. From this related work, we infer that researchers have used pre-selected classes of radiomic and hand-crafted features for survival prediction tasks. Authors use pre-selected three or four classes of radiomic features or hand-crafted features for the survival prediction task. Leveraging the literature, we perform a detailed comprehensive analysis of feature extraction, feature selection, and model selection methods to understand the medical images for the survival prediction task.

Table 1:
Comparison of our work with literature.
Sr# Article Feature class Modelsused Accuracy
First order Shape based GLCM GLSZM GLRLM NGTDM GLDM Hand crafted
1 Soltani et al. (Soltani et al., 2021) Yes Yes Yes Yes Yes Yes Yes No LR, RFR, RFC, ANN N/A
2 Baid et al. (Baid et al., 2020) Yes Yes Yes No No No No No NN using MLP, RF 58.49%
3 Guo et al. (Guo et al., 2019) No No No No No No No Yes Gradient Boosted Decision Tree 52%
4 Baid et al. (Baid et al., 2018) Yes Yes Yes No Yes No No No MLP 57.1%
5 Alam et al. (Alam et al., 2018) Yes Yes No No No No No No CNN 37%
6 Gates et al. (Gates et al., 2018) Yes No Yes No Yes Yes No No RF 52
7 Sun et al. (Sun & Zhang, 2018) Yes Yes No No No No No No Ridge Regression N/A
8 Proposed Work Yes Yes Yes Yes Yes Yes Yes Yes LoR, LR, MLPC, RFC, RFR, MLPR, SVM, ANN DTC, DTR, 66%
DOI: 10.7717/peerjcs.1090/table-1

Dataset

We use two datasets containing MRI and CT scanned images of brain tumor and lung cancer to develop models for survival prediction of cancer patients. Particularly, we use the BraTS 2020 (Menze et al., 2014; Bakas et al., 2017; Bakas et al., 2019) and NSCLC Radiomics (Aerts et al., 2014; Clark et al., 2013; Aerts et al., 2019) datasets for this research work. Table 2 describes the list of abbreviations used in the article.

Table 2:
List of abbreviations and acronyms used in the article.
SR# Abbreviation Explanation SR# Abbreviation Explanation
1 LR Linear Regression 25 RFE Recursive Feature Elimination
2 LoR Logistic Regression 26 DICOM Digital Imaging and Communications in Medicine
3 MLPC Multilayer Perceptron Classifier 27 TesA Testing Accuracy
4 MLPR Multilayer Perceptron Regressor 28 MAE Mean Absolute Error
5 RFC Random Forest Classifier 29 RSME Root Square Mean Error
6 RFR Random Forest Regressor 30 SR# Serial number
7 SVM Support Vector Machine 31 FSM Feature selection methods
8 EM Evaluation Metrics 32 FS Features Selected
9 DTC Decision Tree Classifier 33 ANN Artificial Neural Network
10 DTR Decision Tree Regressor 34 MIr Mutual_Info_regression
11 MIc Mutual_Info_classification 35 Fr F-test_regression
12 Fc F-test_classification 36 ML Machine learning
13 MinA Minimum accuracy 37 MaxA Maximum accuracy
14 AD Accuracy difference 38 CT Computed Tomography
15 MRI Magnetic resonance imaging  39 NSCLC Non-Small Cell Lung Cancer
16 GRACE Global Registry of Acute Coronary Events 40 TIMI Thrombolysis In Myocardial Infarction
17 APACHE-II Acute Physiology And Chronic Health Evaluation II 41 NSTEMI Non-ST-segment Elevation Myocardial Infarction
18 PET Positron Emission Tomography 42 CADx Computer-Aided Diagnosis
19 AI Artificial intelligence 43 COVID-19 Coronavirus disease of 2019
20 GLRLM Gray Level Run Length Matrix 44 PBS Pitt Bacteremia Score
21 GLCM Gray Level Co-occurrence Matrix 45 NGTDM Neighbouring Gray Tone Difference Matric
22 RFECV Recursive Feature Elimination with Cross-Validation 46 LASSO Least Absolute Shrinkage and Selection Operator
23 AD Accuracy difference 47 GLSZM Gray Level Size Zone Matrix
24 AIC Akaike Information Criterion 48 AUC Area Under Curve
DOI: 10.7717/peerjcs.1090/table-2

To predict the survival time of patients (brain tumor), we use 236 patients’ magnetic resonance images (MRI) from the BraTS dataset released in 2020. BraTS dataset is released on yearly basis and from 2017 onwards, BraTS is providing information on the survival days of patients along with MRI (Bakas et al., 2017). BraTS contains native (T1), T2-weighted (T2), post-contrast T1-weighted (T1Gd), and T2 Fluid Attenuated Inversion Recovery (T2-FLAIR) volume images of each patient extracted by varying clinical conventions and scanners (Bakas et al., 2017). Also, the ground truth image containing labels of four classes of enhancing tumor (tumor), edema (ED), necrosis and non-enhancing tumor (NCR/NET), and “other” is provided. In addition, the overall survival of each patient is available in days. Each MRI and ground truth image is compressed to neuroimaging informatics technology initiative (NIfTI) records and consists of a 3D image of 240 × 240 × 155 pixels.

We also use the NSCLC dataset containing CT scanned images of lung cancer patients. The dataset contains records of 422 patients and all CT scanned images are accessible as digital imaging and communications in medicine (DICOM) records. There are a series of CT scans available for each patient. In addition, one Segmentation and Radiotherapy Structure Sets DICOM image for each patient as ground truth is available. Each Segmentation and Radiotherapy Structure Sets image contains a manual outline of the 3D volume of the essential gross tumor volume (GTV-1) by a radiation oncologist. Also, gender, overall stage, and death status of patients along with a patient survival time are available as additional clinical info. Please note that BraTS and NSCLC provide anonymized data which limits the acquisition of censoring information of patients. However, standardization and benchmarking of both datasets inherit that patients are observed for the longest possible bucket of time which nullifies the impact of censoring on survival prediction. For instance, BraTs and NSCLC datasets report survival time of patients upto 1,767 days (4.48 years) and 4454 days (12.2 years), respectively.

For patient survival time prediction, the number of days of each patient is provided for each training sample of BraTS and NSCLC dataset. Despite the quantitative labels of overall patient survival time, the BraTS overall patient survival prediction task handles it as a classification task by binning the patient survival days into three bins. We label the patient survival days as 0, 1, and 2 if the survival days fall into the range of 0–300, 300–450, and >450 days, respectively as done by BraTS. Similar binning is applied for the NSCLC dataset as well. Additionally, we randomly split each dataset into training and testing datasets with the ratio of 80:20 respectively. Overall statistics of datasets are given in Table 3.

Methodology

In this section, first, we describe feature extraction and selection methods chosen for the study. Next, we present the machine learning models and evaluation metrics used to benchmark the image features. Finally, we dive into the experimental setup of our article.

Feature extraction and selection

Figure 1 shows the basic flow diagram of our proposed methodology. Our first chosen feature extraction method is radiomic features. Radiomic features extract sub-visual and quantifiable data from the images which can not be obtained from the naked eye. For in-depth analysis, we further categorize radiomic features into 8 classes in accordance with Van Griethuysen et al. (2017). Precisely, radiomic features are categorized into first order, shape based 2D, shape based 3D, Gray-Level Co-Occurrence Matrix (GLCM), Gray Level Run Length Matrix (GLRLM), Gray Level Size Zone Matrix (GLSZM), Neighborhood Grey Tone Difference Matrix (NGTDM), and Gray Level Dependence Matrix (GLDM) features. Table 4 shows the statistics of radiomic feature classes and few example features of every class. First order statistics examines the intensity of pixels in images using standard metrics like energy, 10th percentile, minimum, and median values. For instance, energy of image pixels is calculated using Eq. (1). E = i = 1 N p X i + c 2 where X is the set of Np number of voxels within the ROI and c is optional parameter.

Table 3:
Statistics of BraTS 2020 and NSCLC radiomics dataset.
SR# Dataset Images Image type Image size Disease type #of patients Survival Info
Train Test Total Train Test Total
1 BraTS 2020 369 125 494 MRI 240 ×240 ×155 Brain Tumor 494 189 47 236
2 NSCLSC Radiomics 338 84 422 CT Scan 512 ×512 ×(75–297) Lung cancer 422 338 84 422
DOI: 10.7717/peerjcs.1090/table-3
Flow diagram of our methodology to understand medical images for survival prediction.

Figure 1: Flow diagram of our methodology to understand medical images for survival prediction.

Table 4:
Statistics of feature classes and example features.
SR# Feature class # of Features Example
1 First Order Statistics 19 Energy, 10th Percentile, Median, Mean
2 Shape Based 3D 16 Mesh volume, Surface area, Compactness, Elongation
3 Shape Based 2D 10 Sphericity, Major axis length, Perimeter
4 GLCM 24 Joint energy, Joint average, Sum variance, Sum entropy
5 GLSZM 16 Small area emphasis, Gray level non-uniformity
6 GLRLM 16 Gray level variance, Run percentage, Run variance
7 NGTDM 5 Coarseness feature value, Complexity feature value
8 GLDM 14 Low gray level emphasis, Gray level variance
9 Hand Crafted 36 Brain tumor core x, Whole SV ratio, Edema grad
10 Total 156
DOI: 10.7717/peerjcs.1090/table-4

Shape-based features i.e., volume of voxel, surface area, and area to volume ratio describe the size and shape of tumorous area in the image. For example, the sphericity of 3D image with the volume (V) and area (A) is computed using Eq. (2). s p h e r i c i t y = 36 π V 2 3 A . Sphericity measures the roundness of objects in the image. Similarly, compactness, axis lengths, flatness, and elongation extract the features to understand the shape of tumor in images.

Gray Level Co-occurrence Matrix (GLCM) uses masks to calculate the distance between similar pixel values to extract the correlation in different regions of the image. Like, Cluster Prominence (CP) measures the skewness and symmetry of an image while Inverse Difference Moment (IDM) estimates the local homogeneity. CP and IDM are computed using Eqs. (3) and (4), respectively. CP = a = 1 N g b = 1 N g a + b u x u y 4 p a , b IDM = a = 0 N g 1 p x y a 1 + a 2

where ux and uy represents mean grey level intensities of x and y dimension while p(ab) is normalized value of co-occurrence matrix. Also, px represents the marginal row probability. Likewise, the variants of standard metrics like cluster share, contrast, entropy variance, joint entropy etc. are calculated for GLCM features. Gray Level Run Length Matrix (GLRLM) aggrandizes the GLCM by mapping the consecutive pixels that have the same gray level value. As an example, Gray Level Non-Uniformity (GLN) measures the similarity of gray-level intensity values in the image. Also, the dependency emphasis metrics examine the texture of image by estimating the distribution of pixels dependence. GLN and Short-Run Emphasis (SRE) are calculated using Eqs. (5) and (6), respectively. GLN = i = 1 N g j = 1 N t P i , j | θ 2 N r θ SRE = i = 1 N g b = 1 N d P i , j j 2 N z

where Nr(θ) is the number of runs in the image along angle θ. Like GLRLM, Gray Level Size Zone Matrix (GLSZM) quantifies gray level zones in the connected pixel zones. Similar metrics such as Small Area Emphasis (SAE), Gray Level Non-Uniformity Normalized (GLNN), and Size-Zone Non-Uniformity (SZN) are extracted as GLSZM features.

Neighbouring Gray Tone Difference Matrix (NGTDM) measures the difference between grey level value of center and average value of neighbours. For example, coarseness indicates the spatial rate of change using Eq. (7) Coarseness = 1 i = 1 N g p i s i where si sum of absolute differences for gray level i. Finally, Gray Level Dependence Matrix (GLDM) excerpts grey level dependencies in an image. Precisely, dependency is calculated by measuring pixels connected and dependent to center pixel of image. Features such as Gray Level Variance (GLV), Dependence Entropy (DE), and Low Gray Level Emphasis (LGLE) are derived from variance, entropy, and gray level emphasis metrics, respectively.

In addition, we notice that researchers have experimented with hand-crafted features to analyze the BraTS dataset. Leveraging these features (Guo et al., 2019), we test 36 hand-crafted features like tumor volume, volume ratio, surface area, position of the enhancing tumor etc. for survival prediction. Overall, we test the performance of 156 radiomic and hand-crafted features for the survival prediction of cancer patients.

Feature selection is a process to improve the performance of machine learning models by selecting the most contributing features only (Kira & Rendell, 1992). Therefore, we test the performance of univariate and recursive feature elimination methods. Univariate methods perform a univariate measurable test on features to measure their relationship for selection. Precisely, we choose F-test and mutual information method from the univariate feature selection category. Similarly, recursive feature elimination methods recursively remove the redundant and negligible features after training and analyzing the performance of machine learning models. We use recursive features elimination (RFE) and recursive feature elimination with cross-validation (RFECV) methods for survival prediction. In addition, univariate and recursive methods are tested for both classification and regression tasks.

Machine learning models and evaluation

The scope of our research is to test the performance of supervised machine learning models in the context of survival prediction. In this regard, we choose Decision Tree Classifier (DTC) (Safavian & Landgrebe, 1991), Support Vector Machine (SVM) (Noble, 2006), Logistic Regression (LoR) (Kleinbaum et al., 2002), and Random Forest Classifier (RFC) for classification of survival time. In addition, we test the neural network models of Multilayer Perceptron Classifier (MLPC) (Gardner & Dorling, 1998) and Artificial Neural Network (ANN) (Hassoun et al., 1995). MLP are strictly feed forward neural networks while ANN models can contain loops (Simplilearn, 2022). Similarly, state-of-the-art models of Multilayer Perceptron Regressor (MLPR), Decision Tree Regressor (DTR) Linear Regression (LR) (Montgomery, Peck & Vining, 2012), and Random Forest Regressor (RFR) (Pal, 2005) are tested for regression task. For the evaluation of models, we select standard evaluation metrics. For instance, classification performance is tested using measures of accuracy and Area Under Curve (AUC) (Goutte & Gaussier, 2005; Story & Congalton, 1986). Accuracy is simply the ratio between correctly predicted survival days of patients and the total number of survival patients. Moreover, AUC utilizes the specificity and sensitivity of the model to measure the ability of a classifier to distinguish between classes. Similarly, the regression models are tested using accuracy, Mean Absolute Error (MAE), Root Mean Squared Error (RMSE), and Akaike information criterion (AIC). Absolute Error is a difference between predicted patient survival days and actual patient survival days. The average of absolute errors of all samples is named Mean Absolute Error (MAE). The square root of the average absolute error is called root Mean Squared Error (RMSE). Additionally, AIC is a statistical measure which uses log-likelihood to estimate the quality of trained model.

Experimental setup

We create combinations of different feature classes, feature selection methods, and machine learning models. Our two defined feature classes are radiomic and hand-crafted features. Also, we further merge six grey level features from radiomic features due to their efficacy to create ‘grey level feature’. Precisely, we combine and test GLCM, GLDM, GLRLM, GLSZM, and NGTDM features. Also, we combine the first order and shape-based features. It is pertinent to note that we also merge shape-based 3D and 2D features as ‘shape-based’ features. Moreover, we augment these features with hand-crafted features. For evaluation of these eight feature classes, we formulate 540 combinations of feature classes, six feature selection methods, and ten models. All possible combinations of features, selection methods, and machine learning models are tested. Table 5 shows the sample combinations formulated for evaluation. Furthermore, we train our model using python 3.9 with Anaconda package management installed on Windows 10. We use the default parameters for machine learning models for training.

Table 5:
Example of formulated combinations.
SR# Feature class FSM Model
1 First order Fc LoR
2 Shape based MIc SVM
3 GLCM MIc MLPC
4 Radiomic features MIc SVM
5 GLRLM Fr DTC
6 First order MIr SVM
7 NGTDM MIc RFC
8 Hand crafted features MIc SVM
DOI: 10.7717/peerjcs.1090/table-5

Results

In this section, first, we describe our analysis of the BraTS dataset. Next, the evaluation results of the NSCLC dataset are presented. Finally, we select the best models for survival prediction of patients by analyzing the “stability” of models.

BraTS dataset

We initiate our analysis by extracting the base results of all feature classes without applying feature selection methods. Please note that we adopt five fold cross validation approach to test all models by varying training and testing data distribution (Refaeilzadeh, Tang & Liu, 2009; Nawaz, Khan & Qadri, 2022; Chatterjee et al., 2022; Xu et al., 2021). Tables 6 and 7 shows the result of BraTS dataset for classification and regression models, respectively. We provide the base result and the highest improvement achieved by models after applying feature selection method. Moreover, best performing feature selection method (FSM) and number of top features (FS) selected are also given. Focusing on classification results, we notice that NGTDM features outperform with 63% accuracy using the RF classifier. Also, logistic regression models failed to perform using all features with 48.2% average accuracy. The poor performance of the LoR model is attributed to the redundancy of features (King & Zeng, 2001). Also, the hand-crafted and first-order features perform poorly with up to 47% and 42% accuracy, respectively. Moreover, despite the low accuracy of the DT classifier with all features, the classifier achieves 52% accuracy with GLCM features. The reason is that in the case of GLCM features the classifier learns better rules to predict test data. On the other hand, we observe that generally, RFC models achieve > 49% accuracy except for hand-crafted and shape-based feature classes. In the case of regression, we achieve the highest 52% accuracy using linear regression and MLP models. However, the Root Mean Squared Error (RMSE) of the MLP model is very large highlighting the poor generalizability of the model due to overfitting. In addition, our analysis on a combination of features highlights that combination of first-order and shape-based features achieves 31% accuracy with LoR model. Also, adding the handcrafted features in this combination improves the accuracy by 17%. While the linear regression model shows 37–46% accuracy with the same combination of features. Moreover, maximum 50% accuracy is achieved with the combination of all grey-level features and LoR model. Results also highlight that classification and regression models did not show a significant improvement in results.

Table 6:
Results of classification models on BraTS 2020 dataset.
SR# Feature class EM LoR MLPC SVM RFC DTC ANN
1 First Order TesA 0.3+0.35 0.14+0.43 0.49+0.05 0.52+0.15 0.39+0.16 0.52+0.02
FSM Fc MIc Fc Fc Fr MIc
FS 16 10 6 12 2 7
2 Shape Based TesA 0.42+0.22 0.22+0.34 0.37+0.22 0.45+0.09 0.37+0.1 0.48+0.15
FSM Fc Fc MIr Fc Fr Fr
FS 2 6 3 all 2 7
3 GLCM TesA 0.48+0.07 0.27+0.31 0.41+0.13 0.59+0.03 0.52+0.1 0.52+0.06
FSM Fc Fr Fc MIc Fr Fc
FS 2 6 9 17 13 9
4 GLDM TesA 0.5+0.1 0.51+0.07 0.3+0.28 0.47+0.15 0.33+0.2 0.52+0.06
FSM Fc MIr MIc Fr MIr Fr
FS 2 5 8 6 3 9
5 GLRLM TesA 0.57+0.09 0.26+0.4 0.11+0.48 0.54+0.09 0.29+0.27 0.53+0.1
FSM MIr MIc Fr Fr MIr MIc
FS 5 6 11 8 6 11
6 GLSZM TesA 0.48+0.08 0.34+0.3 0.29+0.27 0.52+0.13 0.45+0.13 0.52+0.11
FSM Fr MIc MIc Fr MIr Fc
FS 3 12 3 6 6 3
7 NGTDM TesA 0.54+0.03 0.4+0.14 0.45+0.08 0.6+0.03 0.4+0.08 0.49+0.06
FSM Fc Fr Fr Fc Fc MIc
FS 2 5 all 4 2 2
8 Radiomic TesA 0.43+0.17 0.14+0.46 0.14+0.52 0.49+0.17 0.33+0.17 0.5+0.16
FSM Fc Fr MIc MIc Fc Fr
FS 2 2 22 all 6 16
9 Hand Crafted TesA 0.42+0.07 0.34+0.25 0.3+0.23 0.47+0.1 0.35+0.18 0.46+0.09
FSM MIr MIr MIr MIr Fc MIc
FS 2 7 9 21 6 6
10 First Order +Shape Based TesA 0.31+0.34 0.13+0.43 0.14+0.43 0.51+0.11 0.4+0.06 0.49+0.08
FSM Fc Fr MIc MIr Fc Fr
FS 2 10 17 17 16 14
11 GLCM+GLDM +GLRLM+GLSZM + NGTDM TesA 0.5+0.14 0.49+0.12 0.24+0.41 0.53+0.08 0.37+0.15 0.57+0.06
FSM Fc MIr MIr Fc Fr Fc
FS 3 20 13 22 15 13
12 Radiomic +Hand Crafted TesA 0.48+0.12 0.49+0.04 0.16+0.39 0.53-0.02 0.29+0.18 0.5+0.03
FSM Fc MIc MIr Fc MIr Fc
FS 14 4 12 19 11 3
13 First Order +Shape Based +Hand Crafted TesA 0.5+0.08 0.31+0.23 0.51+0.06 0.4+0.21 0.34+0.14 0.5+0.06
FSM Fr MIr Fr Fr Fr Fc
FS 16 2 12 21 16 16
DOI: 10.7717/peerjcs.1090/table-6
Table 7:
Regression models results on BraTS 2020 dataset.
SR# Feature class EM LR MLPR RFR DTR
1 First Order TesA 0.43+0.04 0.32+0.2 0.32+0.14 0.41+0.17
MAE 231.64 414.74 243.66 258.35
RMSE 294.48 519.32 328.51 401.63
AIC, p-value −10.90 0.0011 433.62, 0.0011 −7.53, 0.0001 34.39 0.0002
FSM, FS MIr, 15 Fc, 14 MIr,6 MIr, 15
2 Shape Based TesA 0.38+0.1 0.29+0.25 0.38+0.14 0.42+0.16
MAE 206.57 795.47 233.61 345.77
RMSE 268.76 913.05 336.14 487.8
AIC, p-value −2869.70, 0.0007 278.69 0.0001 202.85 0.0003 119.80,0.0024
FSM, FS Fc, 3 MIr, 10 Fr, 2 Fr, 2
3 GLCM TesA 0.4+0.08 0.52+0.07 0.36+0.1 0.44+0.09
MAE 224.04 250.19 234.17 344.6
RMSE 293.36 374.04 327 496.8
AIC, p-value −3.95, 0.0036 371.74, 0.0003 −0.73, 0.0001 23.41, 0.0002
FSM,FS Fr,18 Fc,16 Fr,5 Fr,5
4 GLDM TesA 0.33+0.07 0.3+0.23 0.38+0.1 0.39+0.14
MAE 225.69 325.88 252.74 313.94
RMSE 281.74 442.39 332.64 453.17
AIC, p-value −5.88 0.0003 11.78 0.0015 −5.67, 0.0011 22.71 0.0005
FSM,FS Fr,2 MIr,3 Fr,2 Fr,3
5 GLRLM TesA 0.39+0.07 0.27+0.25 0.48+0.08 0.44+0.09
MAE 232.51 366.56 220.76 338.31
RMSE 287.39 469.85 292.38 500.58
AIC, p-value −6.86, 0.0004 222.75, 0.0006 −10.87, 0.0007 16.71, 0.0002
FSM,FS Fr,4 Fc,2 Fr,4 Fc,3
6 GLSZM TesA 0.42+0.06 0.27+0.24 0.44+0.08 0.38+0.19
MAE 264.95 367.6 232.35 295.58
RMSE 381.33 470.67 305.39 453.94
AIC, p-value 0.032, 0.0021 1267.67, 0.0007 −7.76, 0.0012 16.71, 0.0002
FSM,FS MIr,12 Fc,2 Fc,14 Fr,6
7 NGTDM TesA 0.4+0.03 0.25+0.3 0.44+0.05 0.37+0.18
MAE 227.36 235.77 235.68 288.25
RMSE 293.97 351.65 316.5 441.41
AIC, p-value −3.13, 0.0008 15.89, 0.0002 −9.21, 0.0002 15.08, 0.0004
FSM,FS Fc,5 MIr,5 Fr,5 MIr,5
8 Radiomic TesA 0.49+0.03 0.51+0.03 0.32+0.21 0.37+0.2
MAE 552.94 3227.4 222.29 275.33
RMSE 1013.36 8417.41 274.38 394.79
AIC, p-value −71.18, 0.0017 202.14, 0.0017 −11.61, 0.0002 26.12, 0.0010
FSM,FS Fc,all MIr,19 Fr,5 MIr,7
9 Hand Crafted TesA 0.38+0.09 0.41+0.09 0.27+0.2 0.23+0.25
MAE 227.32 367.31 219.73 305.13
RMSE 306.02 472.31 300.86 425.47
AIC, p-value −1.067, 0.0005 667.62, 0.0011 −0.57, 0.0005 24.04, 0.0003
FSM,FS Fc,19 Fc,2 Fc,9 MIr ,21
10 First Order +Shape Based TesA 0.44+0.06 0.52+0.0 0.41+0.15 0.41+0.14
MAE 220.26 361.01 217.59 241.02
RMSE 281.62 465.08 281.89 314.71
AIC, p-value 0.22, 0.0003 125.87, 0.0014 −6.67, 0.0004 30.51, 0.0003
FSMF,FS Fc,13 Fc,2 Fr,4 Fc,21
11 GLCM+GLDM +GLRLM+GLSZM +NGTDM TesA 0.44+0.02 0.49+0.07 0.4+0.1 0.4+0.13
MAE 236.25 315.92 230.57 281.65
RMSE 294.58 450.55 298.25 390.29
AIC, p-value −6.67, 0.0006 1084.23, 0.0007 −10.07, 0.0002 22.07, 0.0002
FSM,FS Fr,5 Fr,17 Fr,2 Fr,5
12 Radiomic +Hand Crafted TesA 0.49+0.01 0.49+0.03 0.23+0.2 0.4+0.17
MAE 527.28 368.01 238.3 355.77
RMSE 1118.68 476.19 316.04 539.88
AIC, p-value 63.21 0.0014 641.72 0.0006 −4.68 0.0013 35.86 0.0003
FSM,FS Fc,all Fc,9 Fr,21 MIr,16
13 First Order +Shape Based +Hand Crafted TesA 0.38+0.07 0.49+0.01 0.27+0.16 0.49+0.1
MAE 236.24 368.98 281.17 252.02
RMSE 301.57 473.64 389.32 386.22
AIC, p-value −3.47, 0.003 389.87, 0.0020 2.04, 0.0002 23.23, 0.0001
FSM,FS Fr,11 Fc,2 Fr,2 MIc,7
DOI: 10.7717/peerjcs.1090/table-7

Next, we focus on analyzing the performance of machine learning models with top features selected by six feature selection methods. For an extensive analysis of features, the performance of models is evaluated by training the models with top features ranging from two to ‘all’. In this scenario, ‘all’ features represent the base results of the feature class. We observe that the performance of the logistic regression classifier improves from 42% to 64% accuracy as compared to base results with a selection of top two features with the Fc feature selection method. The improvement of 22% accuracy is attributed to the removal of redundant and insignificant from training and testing data. Moreover, the NGTDM class highlights that all features of the class are important for machine learning models and we get the best 54% accuracy with the SVM classifier. In addition, our results depict that selection of only seven hand-crafted features shows an improvement of 25% accuracy.

Our manual analysis of best-performing features infers that age is the most important feature in the prediction of patient survival days. Moreover, results highlight that classification feature selection methods of Fc and MIc outperform other feature selection methods. In general, we conclude that the logistic regression model achieves the best accuracy of 66% with the top five features selected from GLRLM class with the MIr feature selection method. In addition, feature selection methods improve the performance of classification and regression models by 22% and 10% accuracy, respectively. This result infers that classification models are significantly impacted by feature selection methods.

NSCLC dataset

Tables 8 and 9 show base results of classifier and regression models on the NSCLC dataset. Contrary to the BraTS dataset, results show that LoR and LR models achieve >49% accuracy for each feature class. Also, the ANN model shows more than 49% accuracy. The testing shows that the ANN model is not generalizable because the value of accuracy varies from 33% to 68% for each distribution of the dataset. Also, SVM, MLPC, and MLPR models failed to perform because the results of these models vary by running each model multiple times due to the changing distribution of data.

Table 8:
Results of classification models on NSCLC dataset.
SR# Feature class EM LoR MLPC SVM RFC DTC ANN
1 First Order TesA 0.5+0.0 0.32+0.22 0.5+0.02 0.47+0.08 0.42+0.08 0.49+0.01
FSM Fc MIc Fc MIr MIr MIr
FS 2 5 3 4 2 4
2 Shape Based TesA 0.5+0.03 0.52+0.03 0.32+0.2 0.52+0.01 0.49+0.08 0.48+0.04
FSM MIc MIr Fr MIr MIr MIc
FS 8 6 11 2 2 4
3 GLCM TesA 0.51+0.01 0.32+0.22 0.53-0.01 0.48+0.08 0.38+0.11 0.49+0.02
FSM Fc Fc MIr MIr Fr MIr
FS 4 4 14 11 5 19
4 GLDM TesA 0.5+0.02 0.34+0.16 0.26+0.26 0.46+0.1 0.37+0.18 0.48+0.05
FSM MIr MIr MIr MIr MIc Fc
FS 10 4 4 2 2 12
5 GLRLM TesA 0.53+0.04 0.44+0.08 0.37+0.15 0.44+0.09 0.34+0.15 0.47+0.03
FSM MIr Fr Fc MIc MIr MIr
FS 6 4 4 2 14 13
6 GLSZM TesA 0.5+0.02 0.36+0.15 0.35+0.15 0.46+0.06 0.43+0.08 0.49+0.0
FSM Fc Fc Fc MIr MIc Fc
FS 2 2 2 4 4 2
7 NGTDM TesA 0.52+0.02 0.47+0.07 0.32+0.22 0.5+0.07 0.41+0.17 0.49+0.03
FSM Fc MIr MIc MIr MIr MIc
FS all all all 3 5 2
8 Radiomic TesA 0.51+0.03 0.51+0.03 0.49+0.02 0.5+0.04 0.41+0.09 0.5+0.01
FSM Fc MIc MIr MIr MIc Fc
FS 6 2 3 16 11 14
9 First Order +Shape Based TesA 0.51+0.03 0.5+0.04 0.52+0.01 0.5+0.08 0.42+0.09 0.51+0.02
FSM Fc MIr Fc MIr MIr Fc
FS 4 3 5 7 2 2
10 GLCM+GLDM +GLRLM+GLSZM +NGTDM TesA 0.51+0.02 0.5+0.04 0.38+0.15 0.47+0.07 0.41+0.06 0.48+0.05
FSM Fc MIc MIc MIr,MIc Fr
FS 13 2 3 17 22 13
11 Shape Based +GLRLM+NGTDM TesA 0.49+0.05 0.3+0.24 0.48+0.02 0.48+0.06 0.43+0.16 0.5+0.04
FSM Fc MIc Fc MIc MIr MIc
FS 5 2 2 10 2 11
DOI: 10.7717/peerjcs.1090/table-8
Table 9:
Regression models results on NSCLC dataset.
SR# Feature class EM LR MLPR RFR DTR
1 First Order TesA 0.49+0.03 0.35+0.2 0.49+0.05 0.47+0.19
MAE 858.14 867.01 790.89 509.06
RMSE 1203.85 1156.16 1031.55 919.16
AIC, p-value −29.55, 0.0021 −17.38, 0.0029 −27.41, 0.0017 65.26, 0.0007
FSM,FS Fr,10 Fc,3 MIc,8 MIr,2
2 Shape Based TesA 0.47+0.04 0.48+0.04 0.5+0.09 0.4+0.19
MAE 928.24 879.41 687.27 718.04
RMSE 1298.5 1150.78 943.85 1108.15
AIC, p-value −22.89, 0.0012 −19.47, 0.0009 −29.14, 0.0003 74.33, 0.0006
FSM,FS Fc,13 MIr,2 MIr,2 MIr,3
3 GLCM TesA 0.49+0.03 0.5+0.04 0.51+0.04 0.41+0.22
MAE 938.67 830.72 937.02 593.93
RMSE 1208.09 1132.43 1204.82 952.84
AIC, p-value −22.98, 0.0011 −30.77, 0.0009 −3.52, 0.0019 61.20, 0.0018
FSM,FS Fr,14 Fr,10 Fr,5 MIr,2
4 GLDM TesA 0.51+0.0 0.49+0.05 0.52+0.04 0.48+0.13
MAE 942.89 834.05 611.46 659.26
RMSE 1107.04 1140.74 809.24 1104.38
AIC, p-value −26.52, 0.0031 321.19, 0.0014 −28.26, 0.0009 66.59, 0.0005
FSM,FS Fc,2 Fc,8 MIc,2 Fc,2
5 GLRLM TesA 0.5+0.02 0.52+0.05 0.49+0.06 0.48+0.15
MAE 865.31 846.52 730.63 883.05
RMSE 1108.9 1148.12 948.39 1369.78
AIC, p-value −27.27, 0.0025 356.71, 0.0003 −11.23, 0.0021 84.64, 0.0003
FSM,FS Fc,2 Fc,10 MIr,4 Fc,5
6 GLSZM TesA 0.49+0.02 0.33+0.22 0.47+0.06 0.44+0.13
MAE 851.02 853.07 688.84 649.75
RMSE 1104.88 1140.92 907.73 1122.23
AIC, p-value −28.89, 0.0027 −27.94, 0.0035 −16.65, 0.0015 86.97, 0.0009
FSM,FS MIr,3 Fc,2 MIc,2 Fc,2
7 NGTDM TesA 0.51+0.03 0.54+0.01 0.5+0.03 0.47+0.12
MAE 851.04 845.11 755.27 607.07
RMSE 1102.23 1145.89 981.17 992.18
AIC, p-value −25.70,0.0012 23.39,0.0022 −35.74,0.0004 63.25,0.0010
FSM,FS Fc,2 Fc,3 MIc,3 Fc,2
8 Radiomic TesA 0.51+0.0 0.32+0.22 0.5+0.05 0.42+0.18
MAE 855.24 853.32 701.19 782.29
RMSE 1100.16, 0.0028 1148.03, 0.0028 956.90, 0.0013 1169.21, 0.0003
AIC, p-value −25.34, 0.0028 −24.80, 0.0028 −15.96, 0.0013 71.16, 0.0003
FSM,FS Fc,2 Fc,2 MIr,2 MIc,6
9 First Order+ Shape Based TesA 0.47+0.03 0.41+0.14 0.52+0.06 0.44+0.13
MAE 855.24 863.81 700.87 736.83
RMSE 1100.16 1152.2 950.9 1144.94
AIC, p-value −23.40, 0.0023 254.72, 0.0033 −30.68, 0.0011 59.82, 0.0002
FSM,FS Fc,2 Fc,3 MIr,2 MIr,3
10 GLCM+GLDM+ GLRLM+GLSZM +NGTDM TesA 0.5+0.04 0.37+0.18 0.49+0.05 0.45+0.16
MAE 868.84 839.42 773.03 785.29
RMSE 1110.19 1134.89 1004.97 1221.86
AIC, p-value −25.34, 0.0027 −18.16, 0.0008 −16.38, 0.0004 57.72, 0.0040
FSM,FS Fc,2 MIr,2 MIr,4 MIc,2
11 Shape Based+ GLRLM+NGTDM TesA 0.48+0.03 0.45+0.09 0.48+0.08 0.49+0.12
MAE 853.73 853.76 691.05 758.28
RMSE 1124.91 1140.34 951 1206.06
AIC, p-value −21.89, 0.0012 −26.80, 0.0005 4.70, 0.0007 76.80, 0.0002
FSM,FS MIr,17 Fc,2 MIr,2 MIc,2
DOI: 10.7717/peerjcs.1090/table-9

Analyzing the individual feature class, the feature selection method MIr with GLRLM features and the LoR model achieve the highest accuracy of 57%. Moreover, the LoR model with the MIr feature selection method achieves the maximum improvement in accuracy by 0.08%. We also note that models with mutual information feature selection methods achieve better accuracy compared to F-test feature selection methods. The reason for the failure of the F-test feature methods is that they can handle only the linear dependency of features (Scikit-learn developers, 2021a). However, mutual information feature selection methods can handle various types of dependencies between features. Also, this result shows that BraTS has a more linear dependency on features compared to NSCLC. Focusing on a combination of feature classes, results show that the combination of shape-based, GLRLM and NGTDM achieves the highest accuracy of 59% and 61% for classification and regression, respectively.

Next, we shift our focus to comparing the performance of features for BraTS and NSCLC datasets. The comparison shows that grey level features outperform for the prediction of lung cancer patients in the NSCLC dataset. While shape-based and first-order features are among the best-performing features for the BraTS dataset. In addition, for the BraTS dataset, age is selected as the top feature by the best-performing combination of first-order and shape-based features using the LoR model with the Fc feature selection method. On contrary, age is listed as the 5th top feature by the mutual information feature selection method for NSCLC. Also, the logistic regression model shows better performance with >50% accuracy for both datasets. Similarly, the SVM classifier shows a 54% and 52% value of accuracy with GLCM features for BraTS and NSCLC, respectively. While MLP and decision tree regressor failed for both datasets with high root mean square error as shown in Tables 7 and 9.

Stability analysis

Our extensive analysis of combinations of features, feature selection methods and machine learning models signifies the best performing combination. However, as mentioned earlier, the performance of models is varied by changing the distribution of training and testing data. This observation implies that models achieving the best accuracy are not generalized models as well. Hence, we didn’t rely only on the best accuracy of combination to select the final model. For the final selection of classification models, we calculate the stability and Area Under Curve (AUC) of best performing five combinations. We label the combination as stable which fulfils two conditions. First, the minimum and maximum accuracy of the combination did not vary after testing the model on different training and test sets drawn from the data. Second, the combination achieves the highest AUC value highlighting the confidence of the model to measure of separability of classes. In particular, we test each combination using five fold cross validation after varying training and testing data. Table 10 shows the results of testing stability of best-performing combinations for BraTS and NSCLC datasets for classification. The table provides values of feature selection method (FSM), number of top features selected (FS), minimum (MinA) and maximum accuracy (MaxA) achieved in three iterations, Difference between accuracy (AD), and AUC. We notice that LoR model along with its respective features outperforms for classification of NSCLC and BraTS datasets. The model shows zero variance in accuracy and attains the highest AUC values of 0.769 and 0.751 for BraTS and NSCLC, respectively.

Focusing on regression models, Table 11 presents the analysis for regression models for BraTS and NSCLC datasets. Similar to classification, we also rely on minimum change in accuracy to label the stable model. Also, we test Akaike Information Criterion (AIC) to identify the stable models with least AIC value (Sakamoto, Ishiguro & Kitagawa, 1986). The results indicate the superior performance of LR model with zero variance in accuracy. Moreover, these results are further substantiated by lower AIC values of −71.18 and −29.55 for BraTS and NSCLC, respectively. In addition, we manually analyze the top selected features of models. Table 12 shows the top selected features. We note that age and shape-based features are commonly selected features by best-performing models. Interestingly, for BraTS dataset classification, GLCM contrast feature is selected which highlights the contrast between cancerous and non-cancerous cells as a significant feature. However, the NSCLC dataset relies on GLCM cluster prominence showing the symmetry in the image as a prominent feature. The difference in different feature selection for MRI and CT scans is linked to different image fetching techniques.

Table 10:
Model Selection for Classification: BraTS and NSCLC.
Sr# Feature Class Model FSM FS MinA MaxA AD AUC
BraTS
1 GLRLM LoR MIr 5 66 66 0 0.769
2 GLRLM MLPC MIc 6 29 66 37 0.698
3 Radiomic SVM MIc 22 32 66 34 0.509
4 First Order RFC Fc 12 42 67 25 0.386
5 GLCM DTC Fr 13 34 62 28 0.428
6 Radiomic ANN Fr 16 31 66 35 0.425
NSCLC
1 GLRLM LoR MIr 6 54 54 0 0.751
2 NGTDM MLPC MIr all 46 54 8 0.734
3 NGTDM SVM MIc all 32 54 22 0.531
4 First Order+ Shape based RFC MIr 7 48 58 10 0.444
5 NGTDM DTC MIr 5 38 58 20 0.382
6 NGTDM ANN MIc 2 27 52 25 0.424
DOI: 10.7717/peerjcs.1090/table-10
Table 11:
Model selection for regression: BraTS and NSCLC.
Sr# Feature class Model FSM FS MinA MaxA AD AIC
BraTS
1 Radiomic LR Fc all 52 52 0 −71.18
2 GLCM MLPR Fc 16 19 59 40 371.74
3 GLRLM RFR Fr 4 29 56 27 −10.87
4 First Order DTR MIr 15 31 58 27 34.39
NSCLC
1 First Order LR Fr 10 53 53 0 −29.55
2 First Order MLPR Fc 3 50 55 5 −17.38
3 Shape Based RFR MIr 2 54 59 7 −29.14
4 First Order DTR MIr 2 54 66 12 65.26
DOI: 10.7717/peerjcs.1090/table-11
Table 12:
Top five features of LoR and LR model on BraTS and NSCLC dataset.
SR# Dataset Model FS FSM Top features
1 BraTS LoR 5 MIr Age, shape-based (Maximum 2D diameter, Major Axis Length), GLRLM (Gray Level Non-Uniformity), GLCM (Contrast)
LR all Fc Age, shape-based (Least Axis Length, Major Axis Length, Minor Axis Length, Surface Volume Ratio),
2 NSCLC LoR 10 MIr First-order (Root Mean Squared, Mean, shape-based (Major Axis Length), Age, GLRLM (GrayLevelVariance)
LR 10 Fr Age, first-order (90th percentile), GLCM (Cluster Prominence), shape-based (Minor Axis Length, Surface Volume Ratio)
DOI: 10.7717/peerjcs.1090/table-12

Conclusion

The overall survival prediction of cancer patients using medical imaging is a challenging task due to the scarcity of clinical information and complex features. In this research work, we examine medical images to predict the survival time of cancer patients by using MRI/CT scanned images and age. In this regard, we explore the impact of six feature selection methods and 10 machine learning models on brain tumor and lung cancer datasets. Our analysis emphasizes using top features of images selected by uni-variant and mutual-information based feature selection methods. The feature selection improves the accuracy of models up to 98%. In addition, results show that GLRLM features provide the highest 66% and 54% accuracy using the logistic regression model on BraTS 2020 and NSCLC datasets, respectively. Also, we observe that random forest, decision tree, SVM, and ANN models cannot be used to train a generalized model for survival prediction. The results of these models vary with the changing distribution of training and testing data. Moreover, in-depth analysis of the best performing feature highlights the ‘age’ as the most common and contributing feature for survival prediction.

In this article, we utilize statistical methods for feature extraction. In future, we plan to test machine/deep learning-based feature extraction methods like convolutional neural network (CNN) and generative adversarial networks (GANs). Moreover, the scope of work can be extended to other diseases of breast, liver, and bone cancer.

Supplemental Information

Code and data files of the experiment

DOI: 10.7717/peerj-cs.1090/supp-1

ReadMe file for code

DOI: 10.7717/peerj-cs.1090/supp-2

Value of parameters used to train the model on Windows 10 using the python 3.9 installed using Anaconda 64 bit-version

DOI: 10.7717/peerj-cs.1090/supp-3
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