Kyu Sung Choi1,2,3, Seung Hong Choi4,5,6, Bumseok Jeong1,2,3. 1. Graduate School of Medical Science and Engineering, Korea Advanced Institute for Science and Technology (KAIST), Daejeon, Republic of Korea. 2. KAIST Institute for Health Science and Technology, Korea Advanced Institute for Science and Technology (KAIST), Daejeon, Republic of Korea. 3. KAIST Institute for Artificial Intelligence, Korea Advanced Institute for Science and Technology (KAIST), Daejeon, Republic of Korea. 4. Department of Radiology, Seoul National University Hospital, Seoul, Republic of Korea. 5. Department of Radiology, Seoul National University College of Medicine, Seoul, Republic of Korea. 6. Center for Nanoparticle Research, Institute for Basic Science (IBS), Seoul, Republic of Korea.
Abstract
BACKGROUND: The aim of this study was to predict isocitrate dehydrogenase (IDH) genotypes of gliomas using an interpretable deep learning application for dynamic susceptibility contrast (DSC) perfusion MRI. METHODS: Four hundred sixty-three patients with gliomas who underwent preoperative MRI were enrolled in the study. All the patients were immunohistopathologically diagnosed with either IDH-wildtype or IDH-mutant gliomas. Tumor subregions were segmented using a convolutional neural network followed by manual correction. DSC perfusion MRI was performed to obtain T2* susceptibility signal intensity-time curves from each subregion of the tumors: enhancing tumor, non-enhancing tumor, peritumoral edema, and whole tumor. These, with arterial input functions, were fed into a neural network as multi-dimensional inputs. A convolutional long short-term memory model with an attention mechanism was developed to predict IDH genotypes. Receiver operating characteristics analysis was performed to evaluate the model. RESULTS: The IDH genotype predictions had an accuracy, sensitivity, and specificity of 92.8%, 92.6%, and 93.1%, respectively, in the validation set (area under the curve (AUC), 0.98; 95% confidence interval, 0.969-0.991) and 91.7%, 92.1%, and 91.5%, respectively, in the test set (AUC, 0.95; 95% confidence interval, 0.898 - 0.982). In temporal feature analysis, T2* susceptibility signal intensity-time curves obtained from DSC perfusion MRI with attention weights demonstrated high attention on the combination of the end of the pre-contrast baseline, up/downslopes of signal drops, and/or post-bolus plateaus for the curves used to predict IDH genotype. CONCLUSIONS: We developed an explainable recurrent neural network model based on DSC perfusion MRI to predict IDH genotypes in gliomas.
BACKGROUND: The aim of this study was to predict isocitrate dehydrogenase (IDH) genotypes of gliomas using an interpretable deep learning application for dynamic susceptibility contrast (DSC) perfusion MRI. METHODS: Four hundred sixty-three patients with gliomas who underwent preoperative MRI were enrolled in the study. All the patients were immunohistopathologically diagnosed with either IDH-wildtype or IDH-mutant gliomas. Tumor subregions were segmented using a convolutional neural network followed by manual correction. DSC perfusion MRI was performed to obtain T2* susceptibility signal intensity-time curves from each subregion of the tumors: enhancing tumor, non-enhancing tumor, peritumoral edema, and whole tumor. These, with arterial input functions, were fed into a neural network as multi-dimensional inputs. A convolutional long short-term memory model with an attention mechanism was developed to predict IDH genotypes. Receiver operating characteristics analysis was performed to evaluate the model. RESULTS: The IDH genotype predictions had an accuracy, sensitivity, and specificity of 92.8%, 92.6%, and 93.1%, respectively, in the validation set (area under the curve (AUC), 0.98; 95% confidence interval, 0.969-0.991) and 91.7%, 92.1%, and 91.5%, respectively, in the test set (AUC, 0.95; 95% confidence interval, 0.898 - 0.982). In temporal feature analysis, T2* susceptibility signal intensity-time curves obtained from DSC perfusion MRI with attention weights demonstrated high attention on the combination of the end of the pre-contrast baseline, up/downslopes of signal drops, and/or post-bolus plateaus for the curves used to predict IDH genotype. CONCLUSIONS: We developed an explainable recurrent neural network model based on DSC perfusion MRI to predict IDH genotypes in gliomas.
Authors: Andreas Kleppe; Ole-Johan Skrede; Sepp De Raedt; Knut Liestøl; David J Kerr; Håvard E Danielsen Journal: Nat Rev Cancer Date: 2021-01-29 Impact factor: 60.716
Authors: Hugo Layard Horsfall; Paolo Palmisciano; Danyal Z Khan; William Muirhead; Chan Hee Koh; Danail Stoyanov; Hani J Marcus Journal: World Neurosurg Date: 2020-11-25 Impact factor: 2.104