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Oct 13, 2023

Machine Learning methods for Quantitative Radiomic Biomarkers

Scientific Reports volume 5,

Scientific Reports volume 5, Article number: 13087 (2015) Cite this article

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Radiomics extracts and mines large number of medical imaging features quantifying tumor phenotypic characteristics. Highly accurate and reliable machine-learning approaches can drive the success of radiomic applications in clinical care. In this radiomic study, fourteen feature selection methods and twelve classification methods were examined in terms of their performance and stability for predicting overall survival. A total of 440 radiomic features were extracted from pre-treatment computed tomography (CT) images of 464 lung cancer patients. To ensure the unbiased evaluation of different machine-learning methods, publicly available implementations along with reported parameter configurations were used. Furthermore, we used two independent radiomic cohorts for training (n = 310 patients) and validation (n = 154 patients). We identified that Wilcoxon test based feature selection method WLCX (stability = 0.84 ± 0.05, AUC = 0.65 ± 0.02) and a classification method random forest RF (RSD = 3.52%, AUC = 0.66 ± 0.03) had highest prognostic performance with high stability against data perturbation. Our variability analysis indicated that the choice of classification method is the most dominant source of performance variation (34.21% of total variance). Identification of optimal machine-learning methods for radiomic applications is a crucial step towards stable and clinically relevant radiomic biomarkers, providing a non-invasive way of quantifying and monitoring tumor-phenotypic characteristics in clinical practice.

‘Precision oncology’ refers to the customization of cancer care, where practices and/or therapies are being tailored to individual patients. Such customization process can maximize the success of preventive and therapeutic interventions with minimum side effects. Most of the precision oncology related research has centered on the molecular characterization of tumors using genomics based approaches, which require tissue extraction by tumor biopsies. Although several genomics based approaches have successfully been applied in clinical oncology1, there are inherent limitations to biopsy based assays. Tumors are spatially and temporally heterogeneous and repeated tumor biopsies, which increase the risk for a patient, are often required to capture the molecular heterogeneity of tumors. These ethical and clinical challenges related to biopsy-based assays, can be addressed by medical imaging, which is a routine practice for cancer diagnosis and staging in clinical oncology. Unlike biopsies, medical imaging is non-invasive and can provide information regarding the entire tumor phenotype, including the intra-tumor heterogeneity. Furthermore, recent advances in high-resolution image acquisition machines and computational hardware allow the detailed and efficient quantification of tumor phenotypic characteristics. Therefore, medical imaging provides unprecedented opportunities for precision oncology.

"Radiomics", an emerging and promising field, hypothesizes that medical imaging provides crucial information regarding tumor physiology, which could be exploited to enhance cancer diagnostics2. It provides a comprehensive quantification of tumor phenotypes by extracting and mining large number of quantitative imaging features3. Several studies have investigated various radiomic features in terms of their prognostic or predictive abilities and reliability across different clinical settings4,5,6,7,8,9,10. Different studies have shown the discriminating capabilities of radiomic features for the stratification of tumor histology6, tumor grades or stages11 and clinical outcomes8,12,13. Moreover, some studies have reported the association between radiomic features and the underlying gene expression patterns8,14,15.

"Machine-learning" can be broadly defined as computational methods/models using experience (data) to improve performance or make accurate predictions16. These programmable computational methods are capable of "learning" from data and hence can automate and improve the prediction process. Predictive and prognostic models with high accuracy, reliability and efficiency are vital factors driving the success of radiomics. Therefore, it is essential to compare different machine-learning models for radiomics based clinical biomarkers. Like any high-throughput data-mining field, radiomics also underlies the curse of dimensionality17, which should be addressed by appropriate feature selection strategies. Moreover, feature selection also helps in reducing overfitting of models (increasing the generalizability). Thus, in order to reduce the dimensionality of radiomic feature space and enhance the performance of radiomics based predictive models, different feature selection methods18 should be thoroughly investigated. However, as radiomics is an emerging research field, most of the published studies have only assessed the predictive capabilities of radiomic features without putting much emphasis on the comparison of different feature selection and predictive modeling methods. Only few recent studies have investigated the effect of different feature selection and machine learning classification methods on radiomics based clinical predictions19,20, but with limited sample sizes. Furthermore, these studies lacked independent validation of the results, which may restrict the generalizability of their conclusions.

In this study, we investigated a large panel of machine-learning approaches for radiomics based survival prediction. We evaluated 14 feature selection methods and 12 classification methods in terms of their predictive performance and stability against data perturbation. These methods were chosen because of their popularity in literature. Furthermore, publicly available implementations along with reported parameter configurations were used in the analysis, which ensured an unbiased evaluation of these methods. Two independent lung cancer cohorts were used for training and validation, with in total image and clinical outcome data of 464 patients. Feature selection and predictive modeling are considered as the important building blocks for high throughput data driven radiomics. Therefore, our investigation could help in the identification of optimal machine-learning approaches for radiomics based predictive studies, which could enhance the applications of non-invasive and cost-effective radiomics in clinical oncology.

A total of 440 radiomic features were used in the analysis. These radiomic features quantified tumor phenotypic characteristics on CT images and are divided into four feature groups: I) tumor intensity, II) shape, III) texture and IV) wavelet features. Tumor intensity based features estimated the first order statistics of the intensity histogram, whereas shape features described the 3D geometric properties of the tumor. Textural features, derived from the gray level co-occurrence (GLCM)21 and run length matrices (GLRLM)22, quantified the intra-tumor heterogeneity. These textural features were computed by averaging their values over all thirteen directions. Wavelet features are the transformed domain representations of the intensity and textural features. These features were computed on different wavelet decompositions of the original image using a coiflet wavelet transformation. Matlab R2012b (The Mathworks, Natick, MA) was used for the image analysis. Radiomic features were automatically extracted by our in-house developed radiomics image analysis software, which uses an adapted version of CERR (Computational Environment for Radiotherapy Research)23 and Matlab for the preprocessing of medical images. Mathematical definitions of all radiomic features, as well as the extraction methods, were previously described8.

In this study, we employed two NSCLC cohorts from the two different institutes of Netherlands: (1) Lung1:422 NSCLC patients treated at MAASTRO Clinic in Maastricht. (2) Lung2:225 NSCLC patients treated at Radboud University Medical Center in Nijmegen. CT-scans, manual delineations and clinical data were available for all included patients. More details on the included datasets are described in Supplementary-A. We dichotomized the censored continuous survival data using a cutoff time of 2 years. The patients who lived beyond the cutoff time were labeled as 1, whereas the deceased ones were labeled as 0. The objective of the study was to stratify patients into these two labeled survival classes. Two-years is considered as a relevant survival time for NSCLC patients and several other studies have designed their prediction models using a survival cutoff of 2 years24,25,26. We excluded the patients, which were followed for less than 2 years. It resulted in 310 patients in training cohort (Lung1) and 154 patients in validation cohort (Lung2). All the features were normalized using Z-score normalization.

Fourteen feature selection methods based on filter approaches were used in the analysis (Fisher score (FSCR), Relief (RELF), T-score (TSCR), Chi-square (CHSQ), Wilcoxon (WLCX), Gini index (GINI), Mutual information maximization (MIM), Mutual information feature selection (MIFS), Minimum redundancy maximum relevance (MRMR), Conditional infomax feature extraction (CIFE), Joint mutual information (JMI), Conditional mutual information maximization (CMIM), Interaction capping (ICAP), Double input symmetric relevance (DISR)). In order to improve the readability of this manuscript, we have defined all the acronyms related to feature selection methods in Table 1. We chose these methods mainly because of their popularity in literature, simplicity and computational efficiency. Furthermore, publicly available implementations were readily available for these methods27,28, which increases their reusability. Filter methods are feature-ranking methods, which rank the features using a scoring criterion. All filter based feature selection methods can be divided into two categories: univariate methods and multivariate methods. In case of univariate methods, the scoring criterion only depends on the feature relevancy ignoring the feature redundancy, whereas multivariate methods investigate the multivariate interaction within the features and the scoring criterion is a weighted sum of feature relevancy and redundancy. Feature relevancy is a measure of feature's association with the target/outcome variable, whereas feature redundancy is the amount of redundancy present in a particular feature with respect to the set of already selected features. Further description regarding the theoretical formulation of feature selection problem and each of the used feature selection methods can be obtained from Supplementary-B online.

In machine-learning, the classification is considered as a supervised learning task of inferring a function from labeled training data16. The training data consists of a set of examples, where each example is represented as a pair of an input vector (features) and a desired output value (target or category label). The classification algorithm (classifier) analyzes the training data and infers a hypothesis (function), which can be used for predicting the labels of unseen observations. Many classifiers belonging to different areas of computer science and statistics have been proposed in machine-learning literature29. In our study, we used 12 machine-learning classifiers arising from 12 classifier families (Bagging (BAG), Bayesian (BY), Boosting (BST), Decision trees (DT), Discriminant analysis (DA), Generalized linear models (GLM), Multiple adaptive regression splines (MARS), Nearest neighbors (NN), Neural networks (Nnet), Partial least square and principle component regression (PLSR), Random forests (RF) and Support vector machines (SVM)). The acronyms related to classifiers are defined in Table 1. All classifiers were implemented using R package caret30, which provides a nice interface to access many machine-learning algorithms in R. Furthermore, it also provides a user-friendly framework for training different machine-learning models. Classifiers were trained using the repeated (3 repeat iterations) 10 fold cross validation of training cohort (Lung1) and their predictive performance was evaluated in the validation cohort (Lung2) using area under ROC curve (AUC). We used parameter configurations that were previously defined by Fernandez-Delgado et al.31 in a comprehensive comparative study of 179 classifiers and 121 different datasets. We have listed the classification methods along with their parameters and corresponding R packages in Supplementary-C online.

In order to investigate and compare different feature selection and classification methods, we created a three-dimensional parameter grid for the analysis. For each of the 14 feature selection methods, we incrementally selected features ranging from 5 up to 50, with an increment of 5 features (n = 5, 10, 15, 20, … , 50). These subsets of selected features were then evaluated by using each of the 12 machine-learning classifiers and area under ROC curves (AUC).

In order to assess the stability of feature selection methods, we used a stability measure proposed by Yu et al.32 under the hard data perturbation settings33. We quantified the stability of a method as the similarity between the results obtained by the same feature selection method, when applied on the two non-overlapping partitions (of size N/2) of the training cohort (Lung1). To compute similarity between the two resultant feature sets, a weighted complete bipartite graph was constructed, where the two node sets corresponded to the two sets of selected features. The edge weights were assigned as the absolute Spearman correlation coefficient between the features at the nodes. We then applied the Hungarian algorithm34 to identify the maximum weighted matching between the two node sets and then similarity (stability) was quantified as the final matching cost. For each feature selection method, we computed the stability 100 times using a bootstrap approach and reported the median ± std values in the results.

The empirical stability of a classifier was quantified using the relative standard deviation (RSD %) and a bootstrap approach. We first selected 30 representative features using the Wilcoxon based feature selection method WLCX and used them to compute the classifier stability. For each classification method, we trained the model on the subsampled training cohort (size N/2) and validated the performance on the validation cohort using AUC. Subsampling of the training cohort was done 100 times using a bootstrap approach. RSD is the absolute value of the coefficient of variation and is often expressed in percentage. Here, it was defined as

where and were the standard deviation and mean of the 100 AUC values respectively. It should be noted that higher stability in the case of classifiers corresponds to lower RSD values.

In order to identify the highly reliable and accurate methods, we used the median values of AUC and stability as thresholds. We created two rank lists based on AUC & stability and cited the methods as highly accurate and reliable, which ranked in the top half of both the ranked lists. Feature selection methods having stability ≥0.735 (median stability of all feature selection methods) and AUC ≥ 0.615 (median AUC of all feature selection methods) are considered as highly reliable and accurate methods. Similarly, classification methods having RSD ≤ 5.97 (median RSD of all classifiers) and AUC ≥ 0.61 (median AUC of all classifiers) are considered as highly reliable and accurate ones.

There are three main experimental factors, which can potentially affect the prediction of radiomics based survival prediction: feature selection method, classification method and the number of selected features. Multifactor ANOVA was used to quantify the variability in AUC scores contributed by these factors and their interactions. In order to compare the variability contributed by each factor, the estimated variance components were divided by the total variance.

All the analysis was done using R software (R Core Team, Vienna, Austria) version 3.1.2 and Matlab R2012b (The Mathworks, Natick, MA) with Windows 7.

To investigate the machine-learning approaches for prognostic radiomic biomarkers, a total of 440 radiomic features were extracted from the segmented tumor regions of the pre-treatment CT images of two independent NSCLC cohorts. Feature selection and classification training was done using the training cohort Lung1 (n = 310 patients), whereas the validation cohort Lung2 (n = 154 patients) was used to assess the predictive performance [see Fig. 1].

A total of 440 radiomic features were extracted from the segmented tumor regions of the pre-treatment CT images of 464 NSCLC patients.

Feature selection and classification training was done using the training cohort Lung1 (n = 310), whereas Lung2 (n = 154) cohort was used as a validation cohort.

Predictive performance of different feature selection and classification methods was assessed using the area under receiver operator characteristic curve (AUC). Figure 2 depicts the performance of feature selection (in rows) and classification methods (in columns) using 30 selected features, which are the 30 top ranked features, resulted in feature selection. For each classification method, there are 14 AUC values corresponding to the 14 different feature selection methods. We used a median of all 14 AUC values as a representative AUC of a classifier. Similarly, for each feature selection method, a median of 12 AUCs (corresponding to 12 classification methods) is used as a representative AUC. These representative AUC values for the classification and feature selection methods are given in Table 2. For classification methods, random forest (RF) displayed highest predictive performance (AUC: 0.66 ± 0.03) (median ± std), whereas decision tree (DT) (AUC: 0.54 ± 0.04) showed the lowest predictive performance. As far as feature selection methods are concerned, the Wilcoxon test based method WLCX showed highest predictive performance (AUC: 0.65 ± 0.02), whereas method CHSQ (AUC: 0.60 ± 0.03) and CIFE (AUC: 0.60 ± 0.04) had the lowest median AUCs. We repeated the above experiment by varying the number of selected features (range 5–50). Results corresponding to 10, 20, 40 and 50 representative (top ranked) features are reported in Supplementary Figures S1, S2, S3 and S4 online. Furthermore, median AUC values over each of the experimental factors (feature selection methods, classification methods and number of selected features) are depicted by the heatmaps in Supplementary Figures S5, S6 and S7 online. Here as well, random forest (RF) (classifier) and Wilcoxon test based method WLCX (feature selection) showed highest median AUCs in majority of cases.

Heatmap depicting the predictive performance (AUC) of feature selection (in rows) and classification (in columns) methods.

It can be observed that RF, BAG and BY classification methods and feature selection methods WLCX, MRMR and MIFS shows relatively high predictive performance in many cases.

We assessed the feature selection methods in terms of their stability against data resampling using the hard data perturbation settings33. We observed that MIM was the most stable method (stability = 0.94 ± 0.02) (median ± std) followed by RELIEF (stability = 0.91 ± 0.05) and WLCX (stability = 0.84 ± 0.05), whereas GINI (stability = 0.68 ± 0.10), JMI (stability = 0.68 ± 0.05), CHSQ (stability = 0.69 ± 0.09), DISR (stability = 0.69 ± 0.05) and CIFE (stability = 0.69 ± 0.05) showed relatively low stability [Table 2].

Empirical stability of classification methods was quantified using the relative standard deviation (RSD) and a bootstrap approach. We observed that BY was the most stable classification method (RSD = 0.86%) followed by GLM (RSD = 2.19%), PLSR (RSD = 2.24%) and RF (RSD = 3.52%). BST had the highest relative standard deviation in AUC scores (RSD = 8.23%) and hence the lowest stability among the classification methods. RSD (%) values corresponding to all 12 classifiers are reported in Table 2.

Scatterplots in Fig. 3 assesses the stability and prediction performance. It can be observed that feature selection methods WLCX (stability = 0.84 ± 0.05, AUC = 0.65 ± 0.02), MIFS (stability = 0.8 ± 0.03, AUC = 0.63 ± 0.03), MRMR (stability = 0.74 ± 0.03, AUC = 0.63 ± 0.03) and FSCR (stability = 0.78 ± 0.08, AUC = 0.62 ± 0.04) should be preferred as their stability and predictive performance was higher than the corresponding median values across all feature selection methods (stability = 0.735, AUC = 0.615). Similarly for classification methods, RF (RSD = 3.52%, AUC = 0.66 ± 0.03), BY (RSD = 0.86%, AUC = 0.64 ± 0.05), BAG (RSD = 5.56%, AUC = 0.64 ± 0.03), GLM (RSD = 2.19%, AUC = 0.63 ± 0.02) and PLSR (RSD = 2.24%, AUC = 0.63 ± 0.02), the stability and predictive performance was higher than the corresponding median values (RSD = 5.93%, AUC = 0.61).

Scatterplots between the stability and predictive performance (AUC) of feature selection (FS) (Left) and classification methods (CF) (right).

Feature selection methods having stability ≥0.735 (median stability of FS) and AUC ≥ 0.615 (median AUC of FS) are considered as highly reliable and predictive methods. Similarly, classification methods having RSD ≤ 5.97 (median RSD of CF) and AUC ≥ 0.61 (median AUC of CF) are considered as highly reliable and accurate ones. Highly reliable and predictive methods are displayed in a gray square region.

To quantify the effects of the three experimental factors (feature selection methods, classification methods and the number of selected features), we performed multifactor analysis of variance (ANOVA) on AUC scores. We observed that all three experimental parameters and their interactions are the significant factors affecting the prediction performance [Fig. 4]. Classification method was the most dominant source of variability as it explained 34.21% of the total variance in AUC scores. Feature selection accounted for the 6.25%, whereas interaction of classifier & feature selection explained 23.03% of the total variation. Size of the selected (representative) feature subset only shared 1.65% of the total variance [Fig. 4].

Variation of AUC explained by the experimental factors and their interactions.

It can be observed that classification method was the most dominant source of variability. Size of the selected (representative) feature subset shared the least of the total variance.

Medical imaging is a routinely used and easily accessible source of information in clinical oncology. It serves as a non-invasive and cost-effective cancer diagnostic tool. Radiomics employs the medical imaging data for the customization of cancer care and hence adds a new and promising dimension to precision oncology2,3,8. Moreover, it can also capture the intra-tumor heterogeneity, which is often considered as an important biomarker in oncology12,35,36,37. A number of studies have built radiomics based predictive models for various clinical factors (tumor grades, survival outcomes, treatment response, etc.)12. For the successful realization of radiomics based predictive analyses, it is required to evaluate and compare different feature selection and predictive modeling methods, which was the primary objective of this study.

Various feature selection methods have been employed for high-throughput data mining problems38. In general, feature selection methods are categorized into three main categories: (1) filter methods (2) wrapper methods and (3) embedded methods. In this study, we investigated 14 different filter based approaches for radiomics based survival prediction. We only used filter-based approaches because they are computationally more efficient and less prone to overfitting than the wrapper and embedded methods18,27. Furthermore, unlike wrapper and embedded methods, filter methods are classifier independent. Thus, they allow separation of the modeling and feature selection component of the predictive analysis, which increases the generalizability of each component and hence the overall analysis.

We also investigated 12 machine-learning classification methods belonging to 12 different classifier families. Many classifiers have been proposed in the machine-learning literature. Theoretically speaking, these classifiers belong to different fields (classifier families) of computer science and statistics. Therefore, it could really be difficult to understand the underlying assumptions of each and every classifier and tune the parameters in an unbiased manner. The parameter tuning could be biased by user's more (or lack of) expertise with some classifiers over the others. Usually, the studies, which propose a new classifier, only compare it to the reference classifiers of same family excluding the other classifier families. Even if classifiers belonging to different families are considered for comparison, these reference classifiers are usually implemented using simple tools and with limited parameter configurations while carefully tuning the proposed classifier. These could consequently bias the results in favor of the proposed classifiers31. In our study, we are not proposing any new classifier and we have used the same implementation tool (R package caret) for all the classifiers. Furthermore, to ensure unbiased usage of classifiers, we used parameter configurations that were previously defined by Fernandez-Delgado et al.31, in an exhaustive study of comparing 179 classifiers over 121 different datasets. These parameter configurations were selected from the literature and have been previously validated on a large number (121) of datasets belonging to different fields. Furthermore, in our study, the parameters were tuned using the repeated cross validation of training data only. Hence, our experimental design allowed us to evaluate different classification methods in an unbiased manner.

Our results show that the Wilcoxon test based feature selection method WLCX yields the highest predictive performance with the majority of classifiers. Interestingly, WLCX is a simple univariate method based on ranks, which does not take into account the redundancy of selected features during feature ranking. The majority of feature selection methods gave highest predictive performance when used with the random forest (RF) classifier. One could argue that with different parameter configurations, the performance of classification methods may improve further. An exhaustive parameter tuning could be investigated for evaluating the improvement of prediction performance. However, the required computational resources and high time complexity can hinder the exhaustive search. We expect that future radiomic studies focusing on different clinical outcomes and similar analysis framework could provide better understanding in this regard. A limited number of methods, which are consistently high performing across different radiomic studies, could be further assessed with an exhaustive parameter tuning. Nevertheless, It should be noted that random forests (RF) have displayed high predictive performance in several other biomedical and other domain applications as well31. These results indicate that choosing the WLCX feature selection method and/or RF classification method increases predictive performance in radiomics.

Results related to our stability analysis provide another dimension for choosing the feature selection and classification methods. Depending upon the applications, one may give importance to the predictive performance or stability and accordingly opt for the required method. Results related to multifactor ANOVA indicated that the classification method is the most dominant source of variation in the prediction performance (AUC) and hence should be chosen carefully. Size of the selected feature subset contributed the least in the total variation of AUC.

Only few studies have investigated and compared different feature selection and machine-learning modeling methods for radiomics based clinical predictions19,20. Recently, Hawkins et al.19 have compared four different feature selection and classification methods for CT based survival prediction of NSCLC patients. This study, however, was limited by the small cohort size as the final results were obtained on only 40 patients. Furthermore, it also lacked an independent validation of the results. On the contrary, two independent radiomic cohorts of sizes 310 and 154 patients were used in our analysis and an independent validation of the results was reported.

Our radiomic analysis is focused on the prediction of two-year patient survival in NSCLC patients. It provides an unbiased evaluation of different machine-learning methods of feature selection and classification. It could be considered as a reference for the future radiomics based predictive studies. Our results indicated that choosing Wilcoxon test based feature selection method WLCX and/or random forest (RF) classification method gives highest performance for radiomics based survival prediction. Furthermore, these methods also turned out reasonably stable against data perturbation and hence they could be preferred for radiomics based predictive studies. These results should be further tested in other radiomics based predictive studies, with different imaging modalities and in different cancer types.

It has been previously shown that for NSCLC patients, statistical models based on patient's tumor and treatment characteristics provide significantly better predictions than the human expert24. Moreover, several other studies have highlighted the limitation of doctors’ prognostic capability for terminally ill cancer patients39,40,41. The predictions of human experts can suffer from inter-observer variability. On the contrary, statistical models could make the prediction system more deterministic if the parameter configurations and the training framework are fixed.

The potential clinical utility of radiomics based prognostic models has been stated in previous study8. With expanding radiomics cohorts and feature dimensions, we expect higher prediction performance in future radiomic studies. Furthermore, the integrative studies like radiomics-genomics in combination with standard clinical covariates could also improvise the prediction performance and further validate the utility of these methods in clinical practice. Overall, our analysis is a step forward towards the enhancements of radiomics based clinical predictions.

How to cite this article: Parmar, C. et al. Machine Learning methods for Quantitative Radiomic Biomarkers. Sci. Rep. 5, 13087; doi: 10.1038/srep13087 (2015).

Doroshow, J. & Kummar, S. Translational research in oncology-10 years of progress and future prospects. Nat. Rev. Clin. Oncol. 11, 649 (2014).

Article CAS Google Scholar

Lambin, P. et al. Predicting outcomes in radiation oncology—multifactorial decision support systems. Nat. Rev. Clin. Oncol. 10, 27–40 (2013).

Article Google Scholar

Lambin, P. et al. Radiomics: extracting more information from medical images using advanced feature analysis. Eur. J. of Cancer 48, 441–446 (2012).

Article Google Scholar

Coroller, T. P. et al. CT-based radiomic signature predicts distant metastasis in lung adenocarcinoma. Radiothe. Oncol. (2015), http://dx.doi.org/10.1016/j.radonc.2015.02.015 (2015).

Cook, G. J. et al. Are Pretreatment 18F-FDG PET Tumor Textural Features in Non–Small Cell Lung Cancer Associated with Response and Survival After Chemoradiotherapy? J. Nucl. Med. 54, 19–26 (2013).

Article Google Scholar

Ganeshan, B. et al. Non–small cell lung cancer: histopathologic correlates for texture parameters at CT. Radiology 266, 326–336 (2013).

Article Google Scholar

Gevaert, O. et al. Glioblastoma multiforme: exploratory radiogenomic analysis by using quantitative image features. Radiology 273, 168–174 (2014).

Article Google Scholar

Aerts, H. J. et al. Decoding tumour phenotype by noninvasive imaging using a quantitative radiomics approach. Nat. Commun. 5 (2014).

Leijenaar, R. T. et al. Stability of FDG-PET Radiomics features: An integrated analysis of test-retest and inter-observer variability. Acta Oncol. 52, 1391–1397 (2013).

Article CAS Google Scholar

Parmar, C. et al. Robust radiomics feature quantification using semiautomatic volumetric segmentation. PLOS ONE 9, e102107 (2014).

Article ADS Google Scholar

Ganeshan, B., Abaleke, S., Young, R. C., Chatwin, C. R. & Miles, K. A. Texture analysis of non-small cell lung cancer on unenhanced computed tomography: initial evidence for a relationship with tumour glucose metabolism and stage. Cancer Imaging 10, 137 (2010).

Article Google Scholar

Alic, L., Niessen, W. J. & Veenland, J. F. Quantification of heterogeneity as a biomarker in tumor imaging: a systematic review. PLOS ONE 9, e110300 (2014).

Article ADS Google Scholar

Jain, R. et al. Outcome prediction in patients with glioblastoma by using imaging, clinical and genomic biomarkers: focus on the nonenhancing component of the tumor. Radiology 272, 484–493 (2014).

Article Google Scholar

Nicolasjilwan, M. et al. Addition of MR imaging features and genetic biomarkers strengthens glioblastoma survival prediction in TCGA patients. J. Neuroradiol. (2014), 10.1016/j.neurad.2014.02.006. (2014).

Segal, E. et al. Decoding global gene expression programs in liver cancer by noninvasive imaging. Nat. biotechnol. 25, 675–680 (2007).

Article CAS Google Scholar

Mohri, M., Rostamizadeh, A. & Talwalkar, A. Foundations of machine learning. Ch. 1, 1–3, (MIT press, 2012).

Google Scholar

Pękalska, E. & Duin, R. P. The dissimilarity representation for pattern recognition: foundations and applications. Vol. 64 (World Scientific, 2005).

Guyon, I. & Elisseeff, A. An introduction to variable and feature selection. J. Mach. Learn. Res. 3, 1157–1182 (2003).

MATH Google Scholar

Hawkins, S. H. et al. Predicting Outcomes of Nonsmall Cell Lung Cancer Using CT Image Features. IEEE Access 2, 1418–1426 (2014).

Article Google Scholar

Basu, S. et al. in Systems, Man and Cybernetics (SMC), 2011 IEEE International Conference on. 1306–1312 (IEEE).

Haralick, R. M., Shanmugam, K. & Dinstein, I. H. Textural features for image classification. IEEE Trans. Syst., Man Cybern. 6, 610–621 (1973).

Article Google Scholar

Galloway, M. M. Texture analysis using gray level run lengths. Comput. Vision Graph. 4, 172–179 (1975).

Google Scholar

Deasy, J. O., Blanco, A. I. & Clark, V. H. CERR: a computational environment for radiotherapy research. Med. Phys. 30, 979–985 (2003).

Article Google Scholar

Oberije, C. et al. A prospective study comparing the predictions of doctors versus models for treatment outcome of lung cancer patients: a step toward individualized care and shared decision making. Radiothe. Oncol. 112, 37–43 (2014).

Article Google Scholar

Hoang, T., Xu, R., Schiller, J. H., Bonomi, P. & Johnson, D. H. Clinical model to predict survival in chemonaive patients with advanced non–small-cell lung cancer treated with third-generation chemotherapy regimens based on Eastern Cooperative Oncology Group data. J. Clin. Oncol. 23, 175–183 (2005).

Article CAS Google Scholar

Cistaro, A. et al. Prediction of 2 years-survival in patients with stage I and II non-small cell lung cancer utilizing 18F-FDG PET/CT SUV quantifica. Radiol. oncol. 47, 219–223 (2013).

Article Google Scholar

Brown, G., Pocock, A., Zhao, M.-J. & Luján, M. Conditional likelihood maximisation: a unifying framework for information theoretic feature selection. J. Mach. Learn. Res. 13, 27–66 (2012).

MathSciNet MATH Google Scholar

Zhao, Z. et al. Advancing feature selection research. ASU feature selection repository (2010).

Kotsiantis, Sotiris B., Ioannis, D. Zaharakis & Panayiotis, E. Pintelas . Machine learning: a review of classification and combining techniques. Artif. Intell. Rev. 26.3, 159–190 (2006).

Article Google Scholar

Kuhn, M. Building predictive models in R using the caret package. J. Stat. Softw. 28, 1–26 (2008).

Article Google Scholar

Fernández-Delgado, M., Cernadas, E., Barro, S. & Amorim, D. Do we need hundreds of classifiers to solve real world classification problems? J. Mach. Learn. Res. 15, 3133–3181 (2014).

MathSciNet MATH Google Scholar

Yu, L., Ding, C. & Loscalzo, S. in Proceedings of the 14th ACM SIGKDD international conference on Knowledge discovery and data mining. 803-811 (ACM).

Haury, A.-C., Gestraud, P. & Vert, J.-P. The influence of feature selection methods on accuracy, stability and interpretability of molecular signatures. PLOS ONE 6, e28210 (2011).

Article CAS ADS Google Scholar

Kuhn, H. W. The Hungarian method for the assignment problem. Naval Res. Logis. Q. 2, 83–97 (1955).

Article MathSciNet Google Scholar

Fisher, R., Pusztai, L. & Swanton, C. Cancer heterogeneity: implications for targeted therapeutics. Br. J Cancer 108, 479–485 (2013).

Article CAS Google Scholar

Ng, C., Pemberton, H. & Reis-Filho, J. Breast cancer intratumor genetic heterogeneity: causes and implications. Expert Rev. Anticancer Ther. 12, 1021–1032 (2012).

Article CAS Google Scholar

Brown, J. R., DiGiovanna, M. P., Killelea, B., Lannin, D. R. & Rimm, D. L. Quantitative assessment Ki-67 score for prediction of response to neoadjuvant chemotherapy in breast cancer. Lab. Invest. 94, 98–106 (2014).

Article CAS Google Scholar

Bolón-Canedo, V., Sánchez-Maroño, N., Alonso-Betanzos, A., Benítez, J. & Herrera, F. A review of microarray datasets and applied feature selection methods. Inform. Sciences 282, 111–135 (2014).

Article Google Scholar

Christakis, N. A., Smith, J. L., Parkes, C. M. & Lamont, E. B. Extent and determinants of error in doctors’ prognoses in terminally ill patients: prospective cohort studyCommentary: Why do doctors overestimate? Commentary: Prognoses should be based on proved indices not intuition. Bmj 320, 469–473 (2000).

Article CAS Google Scholar

Glare, P. et al. A systematic review of physicians’ survival predictions in terminally ill cancer patients. Bmj 327, 195 (2003).

Article Google Scholar

Clément-Duchêne, C., Carnin, C., Guillemin, F. & Martinet, Y. How accurate are physicians in the prediction of patient survival in advanced lung cancer? Oncologist 15, 782–789 (2010).

Article Google Scholar

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Authors acknowledge financial support from the National Institute of Health (NIH-USA U24CA194354 and NIH-USA U01CA190234), EU 7th framework program (EURECA, ARTFORCE), Kankeronderzoekfonds Limburg from the Health Foundation Limburg and the Dutch Cancer Society (KWF UM 2009–4454, KWF MAC 2013–6425).

Parmar Chintan and Grossmann Patrick contributed equally to this work.

Departments of Radiation Oncology,

Chintan Parmar, Patrick Grossmann & Hugo J. W. L. Aerts

Radiology, Dana-Farber Cancer Institute, Brigham and Women's Hospital, Harvard Medical School, Boston, MA, USA

Hugo J. W. L. Aerts

Radiation Oncology (MAASTRO), Research Institute GROW, Maastricht University, Maastricht, the Netherlands

Chintan Parmar & Philippe Lambin

Machine Intelligence Unit, Indian Statistical Institute, Kolkata, India

Chintan Parmar

Department of Biostatistics & Computational Biology, Dana-Farber Cancer Institute, Boston, MA, USA

Patrick Grossmann & Hugo J. W. L. Aerts

Department of Radiation Oncology, Radboud University Medical Center, Nijmegen, the Netherlands

Johan Bussink

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H.J.W.L.A., C.P. and P.G. conceived of the project, analysed the data and wrote the paper. J.B. and P.L. provided expert guidance, data, or analysis tools and reviewed the manuscript.

The authors declare no competing financial interests.

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Parmar, C., Grossmann, P., Bussink, J. et al. Machine Learning methods for Quantitative Radiomic Biomarkers. Sci Rep 5, 13087 (2015). https://doi.org/10.1038/srep13087

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Received: 02 April 2015

Accepted: 17 July 2015

Published: 17 August 2015

DOI: https://doi.org/10.1038/srep13087

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