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Imaging-genomics reveals driving pathways of MRI derived volumetric tumor phenotype features in Glioblastoma
- Patrick Grossmann†1, 2Email authorView ORCID ID profile,
- David A. Gutman†3, 4,
- William D. DunnJr3, 4,
- Chad A. Holder5 and
- Hugo J. W. L. Aerts1, 2, 6
© The Author(s). 2016
Received: 28 September 2015
Accepted: 1 August 2016
Published: 8 August 2016
Glioblastoma (GBM) tumors exhibit strong phenotypic differences that can be quantified using magnetic resonance imaging (MRI), but the underlying biological drivers of these imaging phenotypes remain largely unknown. An Imaging-Genomics analysis was performed to reveal the mechanistic associations between MRI derived quantitative volumetric tumor phenotype features and molecular pathways.
One hundred fourty one patients with presurgery MRI and survival data were included in our analysis. Volumetric features were defined, including the necrotic core (NE), contrast-enhancement (CE), abnormal tumor volume assessed by post-contrast T1w (tumor bulk or TB), tumor-associated edema based on T2-FLAIR (ED), and total tumor volume (TV), as well as ratios of these tumor components. Based on gene expression where available (n = 91), pathway associations were assessed using a preranked gene set enrichment analysis. These results were put into context of molecular subtypes in GBM and prognostication.
Volumetric features were significantly associated with diverse sets of biological processes (FDR < 0.05). While NE and TB were enriched for immune response pathways and apoptosis, CE was associated with signal transduction and protein folding processes. ED was mainly enriched for homeostasis and cell cycling pathways. ED was also the strongest predictor of molecular GBM subtypes (AUC = 0.61). CE was the strongest predictor of overall survival (C-index = 0.6; Noether test, p = 4x10−4).
GBM volumetric features extracted from MRI are significantly enriched for information about the biological state of a tumor that impacts patient outcomes. Clinical decision-support systems could exploit this information to develop personalized treatment strategies on the basis of noninvasive imaging.
Glioblastoma (GBM) is a highly invasive and diffuse WHO grade IV tumor and is the most lethal central nervous system malignancy with an annual age-adjusted incidence rate of 3.19/100,000 per population . Despite aggressive surgical therapy, radiation therapy, and temozolomide administration the 2-year survival rate remains around 27 % . As a result, recent investigations have focused on capitalizing on the high molecular heterogeneity of gliomas to develop personalized treatment strategies .
As the underlying drivers of these phenotypes are biological in nature, recent efforts have been conducted indicating underlying genetic characteristics of imaging features. For example, tumor “Ring Enhancement” was found to be significantly associated with unmethylated MGMT promoter status [4, 5], which is known to be a biomarker for response to temozolomide and survival. Similarly, “Contrast Enhancement” and “Mass Effect” imaging features were found to be strongly correlated with expression of groups of genes involved in hypoxia and proliferation, respectively . However, a systematic classification of tumor phenotype features in terms of their underlying cell biological processes on a genome-wide scale in GBM remains absent, although clinical applicability of these image features will depend on knowledge about how these features are driven by tumor biological processes that determine disease progression.
In this study, we present an Imaging-Genomics analysis to investigate the associations of a large set of biological processes and presurgical diagnostic MRI derived quantitative volumetric tumor phenotype features, such as Necrosis or Edema, focusing on the publicly available GBM dataset from The Cancer Genome Atlas (TCGA). These analyses were tied to molecular subtypes in GBM and prognostics. Image based volumetric features provide noninvasive tumor phenotype information complementary to genomic technologies and clinical information, potentially allowing advances in patient stratification and clinical decision-making.
Magnetic resonance imaging
DICOM formatted files of presurgical T1 and T2 sequence magnetic resonance images (MRIs) were accessed and downloaded in November 2014 from TCIA (https://wiki.cancerimagingarchive.net/display/Public/TCGA-GBM), a large archive of medical images of cancer patients who have matched molecular data at The Cancer Genome Atlas (TCGA). Cases that had both T1 and T2-FLAIR images available, were of reasonable quality to perform tumor segmentation, and had presurgical negative status were included. As the presurgical status of an image is not explicitly included in the TCIA data, presurgical status was verified to the best of our ability by a trained neuroradiologist (CH, 17 years of experience) by examining the skull surrounding the tumor for signs of surgeries. The patients in our study were originally imaged at Thomas Jefferson University Hospital and Henry Ford Hospital.
Images of sufficient quality were next analyzed for volumetric features. Briefly, 2D masks which were annotated using FSLView, a module in the FMRIB Software Library 5.0 (FSL ), were applied surrounding the tumor regions on the post gadolinium (GD) contrast T1-weighted images and T2-weighted images. For the T1 images, a single contour was segmented including both the dark (Necrotic or NE) and bright (Contrast Enhancement or CE) areas, and the entire volume was referred to as Tumor Bulk (TB). The pixels contained in these masks were then clustered into dark (NE) and bright (CE) areas by K-means clustering using the FSL FEAT (fMRI Expert Analysis Tool, Version 5.0). The area volume contained within the mask of the T2 FLAIR image set encompasses the Edema (ED) envelope, including regions of hyperintense signal and inclusive of any other abnormal signal in the region previously identified on the T1 (i.e., TB), and was referred to as Total Abnormal Tumor Volume (TV). Afterwards, all masks were visually checked by a trained radiologist (CH). We did not attempt to discriminate between peritumoral edema and non-enhancing tumor, as both appear hyperintense on FLAIR. In addition to the raw volumetric features, we calculated the following feature ratios as investigated in previous studies [8–10] mainly to investigate combined T1/FLAIR signals: NE/TV, CE/TV, ED/TV, TB/TV, NE/CE, and CE/TB. A representation of the tumor volumes analyzed are displayed in Fig. 2.
Matching GBM gene expression (mRNA) data for the TCIA patient cohort was obtained from TCGA using the CBioPortal  with the ‘cgdsr’ R package version 1.1.33. The profile identifier ‘gbm_tcga_pub_mrna_median_Zscores’ was used together with the case identifier ‘gbm_tcga_pub_mrna’ to download the expression values of 18,055 genes given as median Z-scores across the Agilent, Affymetrix U133, and Affymetrix Exon platforms. Expression data were downloaded on April 3, 2015, for 91 patients for which also imaging data was available. Based on expression of 1740 genes, Verhaak et al.  classified TCGA-GBM patients into the four molecular GBM subtypes proneural, neural, classical, and mesenchymal, which were functionally annotated by presence of oncogenic events. To test predictive power for subtypes, we downloaded the classification results on TCGA patients by Verhaak et al. from https://tcga-data.nci.nih.gov/docs/publications/gbm_exp/TCGA_unified_CORE_ClaNC840.txt and calculated the multiclass area under curves (AUCs) of the receiver operator characteristic  of the volumetric features. Imaging and subtype data were available for 79 patients.
To quantify the association of a volumetric features with biological processes, preranked Gene Set Enrichment Analysis  (GSEA) version 2.2.0 was performed; gene ranks were calculated for every feature according to -log10(p) r, where r is the Spearman rank correlation coefficient, and p its p-value. GSEA was performed on the C5-BP collection version 5.0 from the Molecular Signature Database  (MSigDB), which contains the expert-curated Gene Ontology  (GO) gene sets for biological processes. Those 583 gene sets containing at least 15 and at most 500 genes were analyzed. We investigated gene sets that were significantly enriched under a false-discovery-rate (FDR) < 0.05 as specified by GSEA to account for multiple hypothesis-testing .
Overall survival data was available for 141 patients with imaging data, and was downloaded from CBioPortal on April 3, 2015. Prognostic associations of volumetric features were assessed with the concordance index (CI) using the ‘survcomp’ package in Bioconductor . All statistical analyses were carried out using R version 3.1.0  on a Linux operating system.
To investigate which biological processes drive volumetric tumor phenotype features in GBM, we performed a pathway analysis based on gene expression profiles using a preranked Gene Set Enrichment Analysis . We compared these results to molecular subtypes in GBM and evaluated the prognostic value.
Volumetric tumor phenotype features in GBM
Biological processes underlying volumetric features
Summary of pathways associated with volumetric tumor phenotype features of the original volumes (top rows) and their ratios (bottom rows)
Biological processes (positive correlation)
Biological processes (negative correlation)
Immune response, apoptosis
Cell cycle, proliferation, replication, DNA repair, DNA metabolic process
Apoptosis, signal transduction, immune system
Synaptogenesis, biogenesis, extracellular structure organization
Defense response, immune response, Nf-kB, signal transduction
Contrast Enhancement/Tumor Volume
Protein complex assembly, signal transduction, biogenesis
Protein complex assembly, defense response, signal transduction, cytokine production, immune response, Nf-kB
Tumor Bulk/Tumor Volume
Signal transduction, protein complex assembly, cytokine, immune response, Nf-kB
Response to other organism, Nf-kB, immune response, locomotory behaviour
Contrast Enhancement/Tumor Bulk
Response to other organism, Nf-kB, immune response, locomotory behaviour
Volumetric feature ratios were associated with a larger number of biological processes than the original features. Signal transduction was associated with all of the ratios we computed; processes involved in immune system were found for all ratios except for CE/TV. CE/TV, TB/TV, and ED/TV were enriched for protein complex assembly. In addition, ED/TV showed positive enrichment for defense response, cytokine production, and Nf-kB. Nf-kB was also found in NE/TV and TB/TV, as well as in NE/CE and CE/TB. Notably, NE/CE and CE/TB were also inversely enriched for inflammation, immune system response pathways, and anti-apoptosis.
Molecular subtypes in GBM
Performances of volumetric features in predicting molecular subtypes of GBM
Contrast Enhancement/Tumor Volume
Tumor Bulk/Tumor Volume
Contrast Enhancement/Tumor Bulk
Prognostic value of volumetrics
The translation of quantitative imaging data into defined clinical settings requires knowledge of how volumetric tumor phenotype features are driven by biological processes that determine the outcome of a patient. This study presents an Imaging-Genomics analysis of presurgical diagnostic MRI derived volumetric features in GBM to evaluate if tumor phenotype features are associated with underlying tumor biology. We found different features to be enriched for different sets of biological processes. Molecular subtypes of GBM were difficult to be predicted by volumetric features. However, four out of five features showed significant prognostic value.
As correlations among our volumetric features were low to moderate in general, this suggests that quantifying each of those areas individually yields complementary information about the tumor phenotype beyond the Total Tumor Volume (TV). Interestingly, we found most of the biological processes to be anti-correlated to pathway expression. The most prevalent pathways were apoptosis, immune system, and signaling pathways, which were observed mainly for Necrosis (NE), Contrast Enhancement (CE), and Tumor Bulk (TB); features that were also significantly prognostic. As those pathways are known drivers of survival outcome [21–23], this hence explains why NE, CE, and TB were found to be prognostic as well. Importantly, all of these features performed significantly better than TV, which highlights that quantification of individual imaging features should be preferred over calculating only the total tumor volume. Our finding that NE is anti-correlated with immune response and prognostic is in line with Gevaert et al. , who also correlated quantitative imaging features of GBM areas to molecular data and who found significant imaging associations to approximately 20 pathways. This analysis, however, differs from our analysis in that Gevaert et al. investigated a single slice of a tumor (in axial view), whereas we performed quantification using the 3D tumor volumes.
Edema (ED) was the only feature that was correlated with homeostasis, cell cycling, and proliferation pathways. Surprisingly, ED was not prognostic in our analysis, although cell cycling and proliferation are known to be involved in carcinogenesis . However, using the publicly available MRI scoring scheme VASARI (https://wiki.nci.nih.gov/display/CIP/VASARI), Gutman et al.  found ordinal ED assessment to be not prognostic as well. Interestingly, in a related study by Diehn et al. , binary assessment of ED resulted in significant survival predictions. Similarly, a recent study indicated that an ED volume cutoff of 85’000 mm3 is a significant prognostic factor using Kaplan-Meier analysis ; however, the rationale for this cutoff was not given. Prognostic performance of quantitative ED features could increase in cohorts of extended sample sizes, as ED has been reported to be a univariate predictor of survival in a large patient cohort previously . Furthermore, our analysis suggests that CE and NE are prognostic. This is partially in line with Gutman et al. , according to whom CE is prognostic, but NE is not. The contradictions between our results and the studies by Diehn et al. and Gutman et al. could be due to the nature of the ED and NE assessments, which in our analysis were continuous, but binary and ordinal in Diehn et al. and Gutman et al., respectively. Likewise, our methodology could be compared to a study by Jamshidi et al. , but comparison remains challenging as their analysis focused on binary imaging traits on a relatively small cohort of patients and a subset of oncogenic pathways only.
Although ED was the only feature that was not prognostic in our analysis, it was the highest predictor of molecular subtypes in GBM instead. This is likely because ED was the only feature that expressed a different volumetric size distribution across molecular subtypes. Similar indications have been given by Gevaert et al. , who found three out of four features that correlated with molecular subtypes to be quantitative Edema features. In general, we found volumetric features to be only moderate predictors of subtypes suggesting that subtypes do not generally alter the size composition of tumor areas in GBM. Furthermore, we could not confirm that the proneural subtype has lower proportions of CE as suggested by Gutman et al. . Poor predictability of Verhaak molecular subtypes by relative cerebral blood volume using T2-weighted MRI has been also described by Jain et al. .
In our analysis, ratios of volumetric features were not significantly prognostic or predictive of GBM subtypes. Generally, many more biological processes were significantly associated with the feature ratios, usually showing a trend towards a mix of pathways associated with the individual features that the ratios were composed of (e.g., NE/TV were enriched for signal transduction and biogenesis). While our study associated MRI volumetric features with biological processes, molecular subtypes, and survival outcome using genome-wide data and aimed at explaining the rationale for why MRI derived volumetric features are associated with survival on a pathway level, other studies have focused on revealing specific genetic variations between MRI features and survival [30–34].
Our analysis was limited to a retrospective dataset. To establish volumetric biomarkers in clinical applications, prospective evaluation of our results will be required. Biological significance could be further validated by analyses of complementary molecular data such as mutational or epigenetic data. Such analyses could provide further insight into why separate quantification of distinct volumetric tumor phenotype features yield different biological and prognostic information. We acknowledge that the prognostic and predictive performances of the volumetric features in the TCGA-GBM dataset were moderate. Heterogeneity of GBM tumors  could be an explanation for this, which limits the definition of a single molecular subtype especially on the basis of single-needle biopsy [36, 37]. As imaging approaches target the entire visible tumor, we however expect in future studies that prognostic performances will drastically increase when Imaging-Genomic cohorts with even larger numbers of samples and standardized image processing become available for GBM.
While our study focused on volumetric phenotype features, alternative definitions of imaging phenotypes are available. This may, for example, include tumor location as this determines the extent of possible resection and hence is a prognostic factor in GBM . In addition to such semantic phenotypes, agnostic phenotyping approaches such as radiomics could be added .
In conclusion, quantitative imaging biomarkers hold great potential, as, unlike traditional biopsies, medical imaging is noninvasive and captures the entire tumor volume. As we have shown, a relationship exists between individual volumetric phenotype features describing local, clinically relevant subareas of GBM tumors and global expression of genes. Knowledge about how these specific tumor areas are related to underlying biological cell processes may allow for advanced patient stratification and treatment decision on the basis of standard medical imaging, but efforts in optimization of prognostic and predictive performances need to continue.
Authors would like to acknowledge the Enterprise Research Infrastructure & Services at Partners Healthcare for their in-depth support and for the provision of the ERISone cluster environment.
Authors acknowledge financial support from the National Institutes of Health (NIH-USA 24CA194354 and NIH-USA U01CA190234).
Availability of data and materials
MRI data is publicly available in DICOM format at TCIA (https://wiki.cancerimagingarchive.net/display/Public/TCGA-GBM). Corresponding gene expression and survival data is publically available at the same site or can be queried using the same identifiers through the cBioPortal (http://www.cbioportal.org/, see Methods).
PG and HJWLA designed the study. PG analyzed the data and drafted the manuscript. DAG performed tumor segmentation on the MRIs. DAG, WDD, and CAH quantified volumetric features. All authors wrote, reviewed, edited, and approved the final manuscript.
The authors declare that they have no competing interests.
No relevant additional authors’ information.
Consent for publication
Ethics approval and consent to participate
Imaging, gene expression, and survival data have been de-identified by The Cancer Imaging Archive (TCIA) and The Cancer Genome Atlas (TCGA) consortia and are publicly available. Thus, no internal approval of an institutional review board was required for this study. Informed consent was collected by the TCGA Research Network.
Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
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