Dataset Information

Association of radiomic imaging features and gene expression profile as prognostic factors in pancreatic ductal adenocarcinoma.

ABSTRACT: In this study, we investigated whether radiomic features of CT image data can accurately predict HMGA2 and C-MYC gene expression status and identify the patient survival time using a machine learning approach in pancreatic ductal adenocarcinoma (PDAC). A cohort of 111 patients with PDAC was enrolled in our study. Radiomic features were extracted using conventional (shape and texture analysis) and deep learning approaches following to segmentation of preoperative CT data. To predict patient survival time, significant radiomic features were identified using a log-rank test. After surgical resection, level of HMGA2 and C-MYC gene expressions of PDAC tumor regions were classified using a support vector machines method. The model was evaluated in terms of accuracy, sensitivity, specificity, and area under the curve (AUC). Besides, inter-reader reliability analysis was used to demonstrate the robustness of the proposed features. The identified features consistently achieved good performance in survival prediction and classification of gene expression status, on images segmented by different radiologists. Using CT data from 111 patients, six features in the segmented region of images were highly correlated with survival time. Using extracted deep features of excised lesions from 47 patients, we observed an average AUC score of 0.90 with an accuracy of 95% in C-MYC prediction (sensitivity: 92% and specificity: 98%). In HGMA2 group, using shape features, the average AUC score was measured as 0.91 with an accuracy of 88% (sensitivity: 89% and specificity: 88%). In conclusion, the radiomic features of CT image can accurately predict the expression status of HMGA2 and C-MYC genes and identify the survival time of PDAC patients.

SUBMITTER: Li K

PROVIDER: S-EPMC6684898 | biostudies-other | 2019

REPOSITORIES: biostudies-other

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Association of radiomic imaging features and gene expression profile as prognostic factors in pancreatic ductal adenocarcinoma.

Li Ke K Xiao Jingjing J Yang Jiali J Li Meng M Xiong Xuanqi X Nian Yongjian Y Qiao Linbo L Wang Huaizhi H Eresen Aydin A Zhang Zhuoli Z Hu Xianling X Wang Jian J Chen Wei W

American journal of translational research 20190715 7

In this study, we investigated whether radiomic features of CT image data can accurately predict HMGA2 and C-MYC gene expression status and identify the patient survival time using a machine learning approach in pancreatic ductal adenocarcinoma (PDAC). A cohort of 111 patients with PDAC was enrolled in our study. Radiomic features were extracted using conventional (shape and texture analysis) and deep learning approaches following to segmentation of preoperative CT data. To predict patient survi ...[more]

PMID: 31396352

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Project description:BackgroundPancreatic ductal adenocarcinoma (PDAC) remains one of the deadliest malignancies to date. The impressively developed stroma that surrounds and modulates the behavior of cancer cells is one of the main factors regulating the PDAC growth, metastasis and therapy resistance. Here, we postulate that stromal and cancer cell compartments differentiate in protein/lipid glycosylation patterns and analyze differences in glycan fragments in those compartments with clinicopathologic correlates.ResultsWe analyzed native glycan fragments in 109 human FFPE PDAC samples using high mass resolution matrix-assisted laser desorption/ionization Fourier-transform ion cyclotron resonance mass spectrometric imaging (MALDI-FT-ICR-MSI). Our method allows detection of native glycan fragments without previous digestion with PNGase or any other biochemical reaction. With this method, 8 and 18 native glycans were identified as uniquely expressed in only stromal or only cancer cell compartment, respectively. Kaplan-Meier survival model identified glycan fragments that are expressed in cancer cell or stromal compartment and significantly associated with patient outcome. Among cancer cell region-specific glycans, 10 predicted better and 6 worse patient survival. In the stroma, 1 glycan predicted good and 4 poor patient survival. Using factor analysis as a dimension reduction method, we were able to group the identified glycans in 2 factors. Multivariate analysis revealed that these factors can be used as independent survival prognostic elements with regard to the established Union for International Cancer Control (UICC) classification both in tumor and stroma regions.ConclusionOur method allows in situ detection of naturally occurring glycans in FFPE samples of human PDAC tissue and highlights the differences among glycans found in stromal and cancer cell compartment offering a basis for further exploration on the role of specific glycans in cancer-stroma communication.

Project description:Photodynamic therapy (PDT) offers localized focal ablation in unresectable pancreatic tumors while tissues surrounding the treatment volume experience a lower light dose, termed photodynamic priming (PDP). While PDP does not cause tissue damage, it has been demonstrated to promote vascular permeability, improve drug delivery, alleviate tumor cell density, and reduce desmoplasia and the resultant internal pressure in pre-clinical evaluation. Preclinical data supports PDP as a neoadjuvant therapy beneficial to subsequent chemotherapy or immunotherapy, yet it is challenging to quantify PDP effects in clinical treatment without additional imaging and testing. This study investigated the potential of radiomic analysis using CT scans acquired before and after PDT to identify areas experiencing PDT-induced necrosis as well as quantify PDP effects in the surrounding tissues. A total of 235 CT tumor slices from seven patients undergoing PDT for pancreatic tumors were examined. Radiomic features assessed included intensity metrics (CT number in Hounsfield Units) and texture analysis using several gray-level co-occurrence matrix (GLCM) parameters. Pre-treatment scans of tumor areas that resulted in PDT-induced necrosis showed statistically significant differences in intensity and texture-based features that could be used to predict the regions that did respond (paired t-test, response versus no response,p < 0.001). Evaluation of PDP effects on the surrounding tissues also demonstrated statistically significant differences, in tumor mean value, standard deviation, and GLCM parameters of contrast, dissimilarity and homogeneity (t-test, pre versus post,p < 0.001). Using leave-one-out cross validation, six intensity and texture-based features were combined into a support-vector machine model which demonstrated reliable prediction of treatment effects for six out of seven patients (ROC curve, AUC = 0.93). This study provides pilot evidence that texture features extracted from CT scans could be utilized as an effective clinical diagnostic prediction and assessment of PDT and PDP effects in pancreatic tumors. (clinical trial NCT03033225).

Dataset Information

Association of radiomic imaging features and gene expression profile as prognostic factors in pancreatic ductal adenocarcinoma.

Publications

Association of radiomic imaging features and gene expression profile as prognostic factors in pancreatic ductal adenocarcinoma.

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