摘要
原文 | 英語 |
---|---|
頁(從 - 到) | 4429-4436 |
頁數 | 8 |
期刊 | Clinical Cancer Research |
卷 | 24 |
發行號 | 18 |
DOIs | |
出版狀態 | 已發佈 - 9月 15 2018 |
ASJC Scopus subject areas
- 腫瘤科
- 癌症研究
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於: Clinical Cancer Research, 卷 24, 編號 18, 15.09.2018, p. 4429-4436.
研究成果: 雜誌貢獻 › 文章 › 同行評審
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TY - JOUR
T1 - Machine learning–based radiomics for molecular subtyping of gliomas
AU - Lu, C.-F.
AU - Hsu, F.-T.
AU - Hsieh, K.L.-C.
AU - Kao, Y.-C.J.
AU - Cheng, S.-J.
AU - Hsu, J.B.-K.
AU - Tsai, P.-H.
AU - Chen, R.-J.
AU - Huang, C.-C.
AU - Yen, Y.
AU - Chen, C.-Y.
N1 - Export Date: 27 October 2018 CODEN: CCREF Correspondence Address: Chen, C.-Y.; Department of Radiology, School of Medicine, College of Medicine, Taipei Medical University, 250 Wuxing Street, Taiwan; email: [email protected] References: Eckel-Passow, J.E., Lachance, D.H., Molinaro, A.M., Walsh, K.M., Decker, P.A., Sicotte, H., Glioma groups based on 1p/19q, IDH, and TERT promoter mutations in tumors (2015) N Engl J Med, 372, pp. 2499-2508; Brat, D.J., Verhaak, R.G., Aldape, K.D., Yung, W.K., Salama, S.R., Cooper, L.A., Comprehensive, integrative genomic analysis of diffuse lower-grade gliomas (2015) N Engl J Med, 372, pp. 2481-2498; Ceccarelli, M., Barthel, F.P., Malta, T.M., Sabedot, T.S., Salama, S.R., Murray, B.A., Molecular profiling reveals biologically discrete subsets and pathways of progression in diffuse glioma (2016) Cell, 164, pp. 550-563; Louis, D.N., Ohgaki, H., Wiestler, O.D., Cavenee, W.K., (2016) World Health Organization Histological Classification of Tumours of The Central Nervous System, , Lyon, France: International Agency for Research on Cancer; 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Hsieh, K.L.-C., Lo, C.-M., Hsiao, C.-J., Computer-aided grading of gliomas based on local and global MRI features (2017) Computer Methods Prog Biomed, 139, pp. 31-38; Zhang, B., Chang, K., Ramkissoon, S., Tanguturi, S., Bi, W.L., Reardon, D.A., Multimodal MRI features predict isocitrate dehydrogenase genotype in high-grade gliomas (2017) Neuro-Oncol, 19, pp. 109-117; Hsieh, K., Chen, C., Lo, C., Radiomic model for predicting mutations in the isocitrate dehydrogenase gene in glioblastomas (2017) Oncotarget, 8, pp. 45888-45897; Kickingereder, P., Burth, S., Wick, A., Gotz, M., Eidel, O., Schlemmer, H.P., Radiomic profiling of glioblastoma: Identifying an imaging predictor of patient survival with improved performance over established clinical and radiologic risk models (2016) Radiology, 280, pp. 880-889; Clark, K., Vendt, B., Smith, K., Freymann, J., Kirby, J., Koppel, P., The Cancer Imaging Archive (TCIA): Maintaining and operating a public information repository (2013) J Digit Imaging, 26, pp. 1045-1057; 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Cheung, W., Hamarneh, G., N-SIFT: N-dimensional scale invariant feature transform (2009) IEEE Trans Image Process, 18, pp. 2012-2021; Scholkopf, B., Smola, A.J., (2002) Learning with Kernels: Support Vector Machines, Regularization, Optimization, and Beyond, , Cambridge, MA: MIT press; Breiman, L., Random forests (2001) Machine Learn, 45, pp. 5-32; Ratsch, G., Onoda, T., Muller, K.-R., Soft margins for AdaBoost (2001) Machine Learn, 42, pp. 287-320; Seiffert, C., Khoshgoftaar, T.M., Van Hulse, J., RusBoost: A hybrid approach to alleviating class imbalance (2010) IEEE Transactions on Systems, 40, pp. 185-197; Guyon, I., Elisseeff, A., An introduction to variable and feature selection (2003) J Machine Learn Res, 3, pp. 1157-1182; Matthews, B.W., Comparison of the predicted and observed secondary structure of T4 phage lysozyme (1975) Biochim Biophys Acta, 405, pp. 442-451; Powers, D.M., Evaluation: From precision, recall and F-measure to ROC, informedness, markedness and correlation (2011) J Mach Learn Tech, 2, pp. 37-63; Mukaka, M.M., A guide to appropriate use of correlation coefficient in medical research (2012) Malawi Med J, 24, pp. 69-71; Hinkle, D.E., Wiersma, W., Jurs, S.G., (2003) Applied Statistics for The Behavioral Sciences, , Boston, MA: Houghton Mifflin College Division; Upadhyay, N., Waldman, A., Conventional MRI evaluation of gliomas (2011) Br J Radiol, 84, pp. S107-S111; Scott, J., Brasher, P.M., Sevick, R.J., Rewcastle, N.B., Forsyth, P.A., How often are nonenhancing supratentorial gliomas malignant? A population study (2002) Neurology, 59, pp. 947-949; Wiestler, B., Capper, D., Holland-Letz, T., Korshunov, A., von Deimling, A., Pfister, S.M., ATRX loss refines the classification of anaplastic gliomas and identifies a subgroup of IDH mutant astrocytic tumors with better prognosis (2013) Acta Neuropathol, 126, p. 443; Law, M., Young, R.J., Babb, J.S., Peccerelli, N., Chheang, S., Gruber, M.L., Gliomas: Predicting time to progression or survival with cerebral blood volume measurements at dynamic susceptibility-weighted contrast-enhanced perfusion MR imaging (2008) Radiology, 247, pp. 490-498; Law, M., Yang, S., Babb, J.S., Knopp, E.A., Golfinos, J.G., Zagzag, D., Comparison of cerebral blood volume and vascular permeability from dynamic susceptibility contrast-enhanced perfusion MR imaging with glioma grade (2004) Am J Neuroradiol, 25, pp. 746-755; Choi, C., Ganji, S.K., DeBerardinis, R.J., Hatanpaa, K.J., Rakheja, D., Kovacs, Z., 2-hydroxyglutarate detection by magnetic resonance spectroscopy in IDH-mutated patients with gliomas (2012) Nat Med, 18, pp. 624-629; Van Cauter, S., Veraart, J., Sijbers, J., Peeters, R.R., Himmelreich, U., De Keyzer, F., Gliomas: Diffusion kurtosis MR imaging in grading (2012) Radiology, 263, pp. 492-501; Raab, P., Hattingen, E., Franz, K., Zanella, F.E., Lanfermann, H., Cerebral gliomas: Diffusional kurtosis imaging analysis of microstructural differences 1 (2010) Radiology, 254, pp. 876-881; Pereira, S., Pinto, A., Alves, V., Silva, C.A., Deep convolutional neural networks for the segmentation of gliomas in multi-sequence MRI (2015) Brainlesion: Glioma, Multiple Sclerosis, Stroke and Traumatic Brain Injuries. Lecture Notes in Computer Science, , Crimi A, Menze B, Maier O, Reyes M, Handels H, editors. Springer: Cham, Switzerland; Nie, D., Zhang, H., Adeli, E., Liu, L., Shen, D., 3D deep learning for multimodal imaging-guided survival time prediction of brain tumor patients (2016) Medical Image Computing and Computer-Assisted Intervention – MICCAI 2016. Lecture Notes in Computer Science, , Ourselin S, Joskowicz L, Sabuncu M, Unal G, Wells W, editors. Springer: Cham, Switzerland; Shin, H.-C., Roth, H.R., Gao, M., Lu, L., Xu, Z., Nogues, I., Deep convolutional neural networks for computer-aided detection: CNN architectures, dataset characteristics and transfer learning (2016) IEEE Trans Med Imaging, 35, pp. 1285-1298
PY - 2018/9/15
Y1 - 2018/9/15
N2 - Purpose: The new classification announced by the World Health Organization in 2016 recognized five molecular subtypes of diffuse gliomas based on isocitrate dehydrogenase (IDH) and 1p/19q genotypes in addition to histologic phenotypes. We aim to determine whether clinical MRI can stratify these molecular subtypes to benefit the diagnosis and monitoring of gliomas. Experimental Design: The data from 456 subjects with gliomas were obtained from The Cancer Imaging Archive. Overall, 214 subjects, including 106 cases of glioblastomas and 108 cases of lower grade gliomas with preoperative MRI, survival data, histology, IDH, and 1p/19q status were included. We proposed a three-level machine-learning model based on multimodal MR radiomics to classify glioma subtypes. An independent dataset with 70 glioma subjects was further collected to verify the model performance. Results: The IDH and 1p/19q status of gliomas can be classified by radiomics and machine-learning approaches, with areas under ROC curves between 0.922 and 0.975 and accuracies between 87.7% and 96.1% estimated on the training dataset. The test on the validation dataset showed a comparable model performance with that on the training dataset, suggesting the efficacy of the trained classifiers. The classification of 5 molecular subtypes solely based on the MR phenotypes achieved an 81.8% accuracy, and a higher accuracy of 89.2% could be achieved if the histology diagnosis is available. Conclusions: The MR radiomics-based method provides a reliable alternative to determine the histology and molecular subtypes of gliomas.
AB - Purpose: The new classification announced by the World Health Organization in 2016 recognized five molecular subtypes of diffuse gliomas based on isocitrate dehydrogenase (IDH) and 1p/19q genotypes in addition to histologic phenotypes. We aim to determine whether clinical MRI can stratify these molecular subtypes to benefit the diagnosis and monitoring of gliomas. Experimental Design: The data from 456 subjects with gliomas were obtained from The Cancer Imaging Archive. Overall, 214 subjects, including 106 cases of glioblastomas and 108 cases of lower grade gliomas with preoperative MRI, survival data, histology, IDH, and 1p/19q status were included. We proposed a three-level machine-learning model based on multimodal MR radiomics to classify glioma subtypes. An independent dataset with 70 glioma subjects was further collected to verify the model performance. Results: The IDH and 1p/19q status of gliomas can be classified by radiomics and machine-learning approaches, with areas under ROC curves between 0.922 and 0.975 and accuracies between 87.7% and 96.1% estimated on the training dataset. The test on the validation dataset showed a comparable model performance with that on the training dataset, suggesting the efficacy of the trained classifiers. The classification of 5 molecular subtypes solely based on the MR phenotypes achieved an 81.8% accuracy, and a higher accuracy of 89.2% could be achieved if the histology diagnosis is available. Conclusions: The MR radiomics-based method provides a reliable alternative to determine the histology and molecular subtypes of gliomas.
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U2 - 10.1158/1078-0432.CCR-17-3445
DO - 10.1158/1078-0432.CCR-17-3445
M3 - Article
SN - 1078-0432
VL - 24
SP - 4429
EP - 4436
JO - Clinical Cancer Research
JF - Clinical Cancer Research
IS - 18
ER -