Structural and advanced imaging in predicting MGMT promoter methylation of primary glioblastoma: a region of interest based analysis

Abstract Background The methylation status of oxygen 6-methylguanine-DNA methyltransferase (MGMT) promoter has been associated with treatment response in glioblastoma(GBM). Using pre-operative MRI techniques to predict MGMT promoter methylation status remains inconclusive. In this study, we investig...

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Main Authors: Yu Han, Lin-Feng Yan, Xi-Bin Wang, Ying-Zhi Sun, Xin Zhang, Zhi-Cheng Liu, Hai-Yan Nan, Yu-Chuan Hu, Yang Yang, Jin Zhang, Ying Yu, Qian Sun, Qiang Tian, Bo Hu, Gang Xiao, Wen Wang, Guang-Bin Cui
Format: Article
Language:English
Published: BMC 2018-02-01
Series:BMC Cancer
Subjects:
Online Access:http://link.springer.com/article/10.1186/s12885-018-4114-2
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language English
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author Yu Han
Lin-Feng Yan
Xi-Bin Wang
Ying-Zhi Sun
Xin Zhang
Zhi-Cheng Liu
Hai-Yan Nan
Yu-Chuan Hu
Yang Yang
Jin Zhang
Ying Yu
Qian Sun
Qiang Tian
Bo Hu
Gang Xiao
Wen Wang
Guang-Bin Cui
spellingShingle Yu Han
Lin-Feng Yan
Xi-Bin Wang
Ying-Zhi Sun
Xin Zhang
Zhi-Cheng Liu
Hai-Yan Nan
Yu-Chuan Hu
Yang Yang
Jin Zhang
Ying Yu
Qian Sun
Qiang Tian
Bo Hu
Gang Xiao
Wen Wang
Guang-Bin Cui
Structural and advanced imaging in predicting MGMT promoter methylation of primary glioblastoma: a region of interest based analysis
BMC Cancer
Glioblastoma
Image feature
Oxygen 6-methylguanine-DNA methyltransferase (MGMT) promoter
Apparent diffusion coefficient (ADC)
3-diminsional pseudo-continuous arterial spin labeling (3D pCASL) imaging
author_facet Yu Han
Lin-Feng Yan
Xi-Bin Wang
Ying-Zhi Sun
Xin Zhang
Zhi-Cheng Liu
Hai-Yan Nan
Yu-Chuan Hu
Yang Yang
Jin Zhang
Ying Yu
Qian Sun
Qiang Tian
Bo Hu
Gang Xiao
Wen Wang
Guang-Bin Cui
author_sort Yu Han
title Structural and advanced imaging in predicting MGMT promoter methylation of primary glioblastoma: a region of interest based analysis
title_short Structural and advanced imaging in predicting MGMT promoter methylation of primary glioblastoma: a region of interest based analysis
title_full Structural and advanced imaging in predicting MGMT promoter methylation of primary glioblastoma: a region of interest based analysis
title_fullStr Structural and advanced imaging in predicting MGMT promoter methylation of primary glioblastoma: a region of interest based analysis
title_full_unstemmed Structural and advanced imaging in predicting MGMT promoter methylation of primary glioblastoma: a region of interest based analysis
title_sort structural and advanced imaging in predicting mgmt promoter methylation of primary glioblastoma: a region of interest based analysis
publisher BMC
series BMC Cancer
issn 1471-2407
publishDate 2018-02-01
description Abstract Background The methylation status of oxygen 6-methylguanine-DNA methyltransferase (MGMT) promoter has been associated with treatment response in glioblastoma(GBM). Using pre-operative MRI techniques to predict MGMT promoter methylation status remains inconclusive. In this study, we investigated the value of features from structural and advanced imagings in predicting the methylation of MGMT promoter in primary glioblastoma patients. Methods Ninety-two pathologically confirmed primary glioblastoma patients underwent preoperative structural MR imagings and the efficacy of structural image features were qualitatively analyzed using Fisher’s exact test. In addition, 77 of the 92 patients underwent additional advanced MRI scans including diffusion-weighted (DWI) and 3-diminsional pseudo-continuous arterial spin labeling (3D pCASL) imaging. Apparent diffusion coefficient (ADC) and relative cerebral blood flow (rCBF) values within the manually drawn region-of-interest (ROI) were calculated and compared using independent sample t test for their efficacies in predicting MGMT promoter methylation. Receiver operating characteristic curve (ROC) analysis was used to investigate the predicting efficacy with the area under the curve (AUC) and cross validations. Multiple-variable logistic regression model was employed to evaluate the predicting performance of multiple variables. Results MGMT promoter methylation was associated with tumor location and necrosis (P <  0.05). Significantly increased ADC value (P <  0.001) and decreased rCBF (P <  0.001) were associated with MGMT promoter methylation in primary glioblastoma. The ADC achieved the better predicting efficacy than rCBF (ADC: AUC, 0.860; sensitivity, 81.1%; specificity, 82.5%; vs rCBF: AUC, 0.835; sensitivity, 75.0%; specificity, 78.4%; P = 0.032). The combination of tumor location, necrosis, ADC and rCBF resulted in the highest AUC of 0.914. Conclusion ADC and rCBF are promising imaging biomarkers in clinical routine to predict the MGMT promoter methylation in primary glioblastoma patients.
topic Glioblastoma
Image feature
Oxygen 6-methylguanine-DNA methyltransferase (MGMT) promoter
Apparent diffusion coefficient (ADC)
3-diminsional pseudo-continuous arterial spin labeling (3D pCASL) imaging
url http://link.springer.com/article/10.1186/s12885-018-4114-2
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spelling doaj-63ddbcf514324ba68f6173e854a4b8702020-11-25T00:42:44ZengBMCBMC Cancer1471-24072018-02-0118111010.1186/s12885-018-4114-2Structural and advanced imaging in predicting MGMT promoter methylation of primary glioblastoma: a region of interest based analysisYu Han0Lin-Feng Yan1Xi-Bin Wang2Ying-Zhi Sun3Xin Zhang4Zhi-Cheng Liu5Hai-Yan Nan6Yu-Chuan Hu7Yang Yang8Jin Zhang9Ying Yu10Qian Sun11Qiang Tian12Bo Hu13Gang Xiao14Wen Wang15Guang-Bin Cui16Department of Radiology & Functional and Molecular Imaging Key Lab of Shaanxi Province, Tangdu Hospital, the Military Medical University of PLA Airforce (Fourth Military Medical University)Department of Radiology & Functional and Molecular Imaging Key Lab of Shaanxi Province, Tangdu Hospital, the Military Medical University of PLA Airforce (Fourth Military Medical University)Department of Medical Image Diagnosis, Hanzhong Central HospitalDepartment of Radiology & Functional and Molecular Imaging Key Lab of Shaanxi Province, Tangdu Hospital, the Military Medical University of PLA Airforce (Fourth Military Medical University)Department of Radiology & Functional and Molecular Imaging Key Lab of Shaanxi Province, Tangdu Hospital, the Military Medical University of PLA Airforce (Fourth Military Medical University)Department of Radiology & Functional and Molecular Imaging Key Lab of Shaanxi Province, Tangdu Hospital, the Military Medical University of PLA Airforce (Fourth Military Medical University)Department of Radiology & Functional and Molecular Imaging Key Lab of Shaanxi Province, Tangdu Hospital, the Military Medical University of PLA Airforce (Fourth Military Medical University)Department of Radiology & Functional and Molecular Imaging Key Lab of Shaanxi Province, Tangdu Hospital, the Military Medical University of PLA Airforce (Fourth Military Medical University)Department of Radiology & Functional and Molecular Imaging Key Lab of Shaanxi Province, Tangdu Hospital, the Military Medical University of PLA Airforce (Fourth Military Medical University)Department of Radiology & Functional and Molecular Imaging Key Lab of Shaanxi Province, Tangdu Hospital, the Military Medical University of PLA Airforce (Fourth Military Medical University)Department of Radiology & Functional and Molecular Imaging Key Lab of Shaanxi Province, Tangdu Hospital, the Military Medical University of PLA Airforce (Fourth Military Medical University)Department of Radiology & Functional and Molecular Imaging Key Lab of Shaanxi Province, Tangdu Hospital, the Military Medical University of PLA Airforce (Fourth Military Medical University)Department of Radiology & Functional and Molecular Imaging Key Lab of Shaanxi Province, Tangdu Hospital, the Military Medical University of PLA Airforce (Fourth Military Medical University)Department of Radiology & Functional and Molecular Imaging Key Lab of Shaanxi Province, Tangdu Hospital, the Military Medical University of PLA Airforce (Fourth Military Medical University)Department of Radiology & Functional and Molecular Imaging Key Lab of Shaanxi Province, Tangdu Hospital, the Military Medical University of PLA Airforce (Fourth Military Medical University)Department of Radiology & Functional and Molecular Imaging Key Lab of Shaanxi Province, Tangdu Hospital, the Military Medical University of PLA Airforce (Fourth Military Medical University)Department of Radiology & Functional and Molecular Imaging Key Lab of Shaanxi Province, Tangdu Hospital, the Military Medical University of PLA Airforce (Fourth Military Medical University)Abstract Background The methylation status of oxygen 6-methylguanine-DNA methyltransferase (MGMT) promoter has been associated with treatment response in glioblastoma(GBM). Using pre-operative MRI techniques to predict MGMT promoter methylation status remains inconclusive. In this study, we investigated the value of features from structural and advanced imagings in predicting the methylation of MGMT promoter in primary glioblastoma patients. Methods Ninety-two pathologically confirmed primary glioblastoma patients underwent preoperative structural MR imagings and the efficacy of structural image features were qualitatively analyzed using Fisher’s exact test. In addition, 77 of the 92 patients underwent additional advanced MRI scans including diffusion-weighted (DWI) and 3-diminsional pseudo-continuous arterial spin labeling (3D pCASL) imaging. Apparent diffusion coefficient (ADC) and relative cerebral blood flow (rCBF) values within the manually drawn region-of-interest (ROI) were calculated and compared using independent sample t test for their efficacies in predicting MGMT promoter methylation. Receiver operating characteristic curve (ROC) analysis was used to investigate the predicting efficacy with the area under the curve (AUC) and cross validations. Multiple-variable logistic regression model was employed to evaluate the predicting performance of multiple variables. Results MGMT promoter methylation was associated with tumor location and necrosis (P <  0.05). Significantly increased ADC value (P <  0.001) and decreased rCBF (P <  0.001) were associated with MGMT promoter methylation in primary glioblastoma. The ADC achieved the better predicting efficacy than rCBF (ADC: AUC, 0.860; sensitivity, 81.1%; specificity, 82.5%; vs rCBF: AUC, 0.835; sensitivity, 75.0%; specificity, 78.4%; P = 0.032). The combination of tumor location, necrosis, ADC and rCBF resulted in the highest AUC of 0.914. Conclusion ADC and rCBF are promising imaging biomarkers in clinical routine to predict the MGMT promoter methylation in primary glioblastoma patients.http://link.springer.com/article/10.1186/s12885-018-4114-2GlioblastomaImage featureOxygen 6-methylguanine-DNA methyltransferase (MGMT) promoterApparent diffusion coefficient (ADC)3-diminsional pseudo-continuous arterial spin labeling (3D pCASL) imaging