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Clinical Article
Whole tumor volume based histogram analysis of ADC signal intensity for differentitating between WHO grade Ⅱ and Ⅲ glioma
LIU Yang-ying-qiu  SHANG Jin  TIAN Shi-yun  SONG Qing-wei  HUANG Ning  GUO Yan  MIAO Yan-wei 

DOI:10.12015/issn.1674-8034.2017.04.008.


[Abstract] Objective: To evaluate the differential diagnostic value of histogram analysis of ADC signal intensity based on entire region of grade Ⅱ and Ⅲ tumor, and then to investigate a potential imaging biomarker to differentiate them.Materials and Methods: Thirteen patients with grade Ⅱ glioma and 20 patients with grade Ⅲ glioma were enrolled in this retrospective study, and all tumors were pathologically confirmed. ROIs containing the entire tumor and peripheral edema were drawn in each slice of the ADC signal intensity maps. Obtained the 3D ROI ADC signal strength histogram information and all its parameters. Histogram related parameters including min intensity, max intensity, mean value, the 10th, 25th, 50th, 75th and 90th percentiles, range, voxel number, standard deviation, variance, mean deviation, skewness, kurtosis and uniformity were recorded. The obtained parameters were compared between groups. Receiver operating characteristic (ROC) curve was constructed to assess the ability of parameters between grade Ⅱ and Ⅲ glioma.Results: Min Intensity (P=0.04), 10th percentiles (P=0.03), voxel number (P=0.003), standard deviation (P=0.022), skewness (P=0.017) showed significant difference between two groups. When optimal cut point of voxel number was 5.46×106 for diagnosis of grade Ⅱ and Ⅲ, the area under the ROC curve was maximum, which was 0.856, the sensitivity and specificity was 81.5%, 80.0%. When optimal cut point of skewness was-1.414, the area under the ROC curve was 0.750, the sensitivity and specificity was 100.0%, 60.0%. When optimal cut point of standard deviation was 14.602, the area under the ROC curve was 0.738, the sensitivity and specificity was 100.0%, 55.0%.Conclusion: Histogram analysis of ADC signal intensity based on entire tumor could provide more information in differentiation of grade Ⅱ and Ⅲ glioma. Voxel number, standard deviation and skewness showed superior diagnostic value.
[Keywords] Glioma;Magnetic resonance imaging;Histogram analysis;Apparent diffusion coefficient;Neoplasm grading

LIU Yang-ying-qiu Department of Radiology, The First Affiliated Hospital of Dalian Medical University, Dalian 116000, China

SHANG Jin Department of Radiology, The First Affiliated Hospital of Dalian Medical University, Dalian 116000, China

TIAN Shi-yun Department of Radiology, The First Affiliated Hospital of Dalian Medical University, Dalian 116000, China

SONG Qing-wei Department of Radiology, The First Affiliated Hospital of Dalian Medical University, Dalian 116000, China

HUANG Ning Life science, GE Healthcare, Shenyang 110000, China

GUO Yan Life science, GE Healthcare, Shenyang 110000, China

MIAO Yan-wei* Department of Radiology, The First Affiliated Hospital of Dalian Medical University, Dalian 116000, China

*Correspondence to: Miao YW, E-mail: ywmiao716@163.com

Conflicts of interest   None.

ACKNOWLEDGMENTS  This work was part of National Nature Science Foundation of China No. 81671646
Received  2016-12-24
Accepted  2017-02-21
DOI: 10.12015/issn.1674-8034.2017.04.008
DOI:10.12015/issn.1674-8034.2017.04.008.

[1]
Schwartzbaum JA, Fisher JL, Aldape KD, et al. Epidemiology and molecular pathology of glioma. Nat Clin Pract Neurol, 2006, 2(9): 494-503.
[2]
Szczepankiewicz F, van Westen D, Englund E, et al. The link between diffusion MRI and tumor heterogeneity: mapping cell eccentricity and density by diffusional variance decomposition (DIVIDE). NeuroImage, 2016, 142: 522-532.
[3]
李治国.脑胶质瘤ADC值及多体素磁共振波谱与肿瘤细胞增殖活性的相关性研究.广州:南方医科大学, 2012.
[4]
Le BD. Apparent diffusion coefficient and beyond: what diffusion MR imaging can tell us about tissue structure. Radiology, 2013, 268(2): 318-322.
[5]
董鑫哲,邢立刚,于金明.肿瘤异质性的医学影像学分析及临床应用.中华肿瘤杂志, 2013, 35(2): 81-84.
[6]
Sternberg EJ, Lipton ML, Burns J. Utility of diffusion tensor imaging in evaluation of the peritumoral region in patients with primary andmetastatic brain tumors. AJNR Am J Neuroradiol, 2014, 35(3): 439-444.
[7]
Catalaa I, Henry R, Dillon WP, et al. Perfusion, diffusion and spectroscopy values in newly diagnosed cerebral gliomas. NMR Biomed, 2006, 19(4): 463-475.
[8]
Murakami R, Hirai T, Kitajima M, et al. Magnetic resonance imaging of pilocytic astrocytomas: usefulness of the minimum apparent diffusion coefficient (ADC) value for differentiation from high-grade gliomas. Acta Radiol, 2008, 49(4): 462-467.
[9]
Murakami R, Hirai T, Sugahara T, et al. Grading astrocytic tumors by using apparent diffusion coefficient parameters: superiority of a one-versus two-parameter pilot method. Radiology, 2009, 251(3): 838-845.
[10]
Arvinda HR, Kesavadas C, Sarma PS, et al. Glioma grading: sensitivity, specificity, positive and negative predictive values of diffusion and perfusion imaging. J Neurooncol, 2009, 94(1): 87-96.
[11]
Lee EJ, Lee SK, Agid R, et al. Preoperative grading of presumptive low-grade astrocytomas on MR imaging: diagnostic value of minimum apparent diffusion coefficient. AJNR Am J Neuroradiol, 2008, 29(10): 1872-1877.
[12]
Cha S. Update on brain tumor imaging: from anatomy to physiology. AJNR Am J Neuroradiol, 2006, 27(3): 475-487.
[13]
Tozer DJ, Jäger HR, Danchaivijitr N, et al. Apparent diffusion coefficient histograms may predict low-grade glioma subtype. NMR Biomed, 2007, 20(1): 49-57.
[14]
Ahn SJ, Choi SH, Kim YJ, et al. Histogram analysis of apparent diffusion coefficient map of standard and high B-value diffusion MR imaging in head and neck squamous cell carcinoma: a correlation study with histological grade. Acad Radiol, 2012, 19(10): 1233-1240.
[15]
Suo ST, Chen XX, Fan Y, et al. Histogram analysis of apparent diffusion coefficient at 3.0 T in urinary bladder lesions: correlation with pathologic findings. Acad Radiol, 2014, 21(8): 1027-1034.
[16]
Ma X, Zhao X, Ouyang H, et al. Quantified ADC histogram analysis: a new method for differentiating mass-forming focal pancreatitis from pancreatic cancer. Acta Radiol, 2014, 55(7): 785-792.
[17]
Woo S, Cho JY, Kim SY, et al. Histogram analysis of apparent diffusion coefficient map of diffusion-weighted MRI in endometrial cancer: a preliminary correlation study with histological grade. Acta Radiol, 2014, 55(10): 1270-1277.
[18]
Cho SH, Kim GC, Jang YJ, et al. Locally advanced rectal cancer: post-chemoradiotherapy ADC histogram analysis for predicting a complete response. Acta Radiol, 2015, 56(9): 1042-1050.
[19]
Provenzale JM, Mukundan S, Barboriak DP. Diffusion-weighted and perfusion MR imaging for brain tumor characterization and assessment of treatment response. Radiology, 2006, 239(3): 632-649.
[20]
Ryu YJ, Choi SH, Park SJ, et al. Glioma: application of whole-tumor texture analysis of diffusion-weighted imaging for the evaluation of tumor heterogeneity. PLoS One, 2014, 9(9): 108335.
[21]
Louis D, Ohgaki H, Wiestler O, et al. The 2007 WHO classification of tumors of the central nervous system. Acta Neuro-pathol, 2007, 114(2): 97-109.
[22]
周仪.颅内钙化的鉴别诊断.实用放射学杂志, 1997, 8(13): 497-498.
[23]
Kang Y, Choi SH, Kim YJ, et al. Gliomas: histogram analysis of apparent diffusion coefficient maps with standard-or high-b-value diffusion-weighted MR imaging-correlation with tumor grade. Radiology, 2011, 261(3): 882-890.
[24]
Alexander CG, Thomas JC, Rajesh CD, et al. Lymphomas and high-grade astrocytomas: comparison of water diffusibility and histologic characteristics. Radiology, 2002, 224(1): 177-183.
[25]
郎志谨,苗延巍,吴仁华,等. MRI新技术及在中枢神经系统肿瘤的应用.上海:上海科学技术出版社, 2015: 15-16.
[26]
Price SJ, Jena R, Burnet NG, et al. Improved delineation of glioma margins and regions of infiltration with the use of diffusion tensor imaging: an image-guided biopsy study. AJNR Am J Neuroradiol, 2006, 27(9): 1969-1974.
[27]
江晶晶.脑肿瘤的分子生物学行为与功能磁共振成像的相关性研究.武汉:华中科技大学, 2014.
[28]
Lu SS, Kim SJ, Kim N, et al. Histogram analysis of apparent diffusion coefficient maps for differentiating primary CNS lymphomas from tumefactive demyelinating lesions. AJR Am J Roentgenol, 2015, 204(4): 827-834.
[29]
Cruz-Sanchez FF, Ferreres JC, Figols J, et al. Prognostic analysis of astrocytic gliomas correlating histological parameters with the proliferating cell nuclear antigen labelling index (PCNA-LI). Histol Histopathol, 1997, 12(1): 43-49.
[30]
肖俊强,卢光明,李苏建,等.磁共振DWI和PWI在胶质瘤术前分级中的应用研究.医学影像学杂志, 2009, 19(4): 376-380.
[31]
颜虹.医学统计学.北京:人民卫生出版社, 2010: 29-32.
[32]
周成丞. IDH1突变胶质瘤磁共振波谱和纹理分析的影像学研究.上海:复旦大学, 2013.
[33]
周水琴.基于核磁共振成像的梨果品质无损检测方法研究.杭州:浙江大学, 2013.
[34]
Zhang YD, Wang Q, Wu CJ, et al. The histogram analysis of diffusion-weighted intravoxel incoherent motion (IVIM) imaging for differentiating the gleason grade of prostate cancer. Eur Radiol, 2015, 25(4): 994-1004.
[35]
Baek HJ, Kim HS, Kim N, et al. Percent change of perfusion skewness and kurtosis: a potential imaging biomarker for early treatment response in patients with newly diagnosed glioblastomas. Radiology, 2012, 264(3): 834-843.
[36]
Louis DN, Perry A, Reifenberger G, et al. The 2016 World Health Oganization classification of tumors of the central nervous system: a summary. Acta Neuropathol, 2016, 131(6): 803-820.

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