Medulloblastoma (MB) is the most common embryonal tumour of the brain. In order to decide on an optimal therapy, laborious inspection of histopathological tissue slides by neuropathologists is necessary. Digital pathology with the support of deep learning methods can help to improve the clinical workflow. Due to the high resolution of histopathological images, previous work on MB classification involved manual selection of patches, making it a time consuming task. In order to leverage only slide labels for histopathology image classification, weakly supervised approaches first encode small patches into feature vectors using an ImageNet pretrained encoder based on convolutional neural networks. The representations of patches are further utilized to train a data-efficient attention-based learning method. Due to the domain shift between natural images and histopathology images, the encoder is not optimal for feature extraction for MB classification. In this study, we adapt weakly supervised learning for MB classification and examine different histopathological specific encoder architectures and weights for the MB classification task. The results show that ResNet encoders pretrained with histopathology images lead to better MB classification results compared to encoders pretrained on ImageNet. The best performing method uses a ResNet50 architecture, pretrained on histopathology images and achieves an area under the receiver operating curve (AUROC) value of 71.89%, improving the baseline model by 2%.
Medulloblastoma (MB) is the most common malignant brain tumor in childhood. The diagnosis is generally based on the microscopic evaluation of histopathological tissue slides. However, visual-only assessment of histopathological patterns is a tedious and time-consuming task and is also affected by observer variability. Hence, automated MB tumor classification could assist pathologists by promoting consistency and robust quantification. Recently, convolutional neural networks (CNNs) have been proposed for this task, while transfer learning has shown promising results. In this work, we propose an end-to-end MB tumor classification and explore transfer learning with various input sizes and matching network dimensions. We focus on differentiating between the histological subtypes classic and desmoplastic/nodular. For this purpose, we systematically evaluate recently proposed EfficientNets, which uniformly scale all dimensions of a CNN. Using a data set with 161 cases, we demonstrate that pre-trained EfficientNets with larger input resolutions lead to significant performance improvements compared to commonly used pre-trained CNN architectures. Also, we highlight the importance of transfer learning, when using such large architectures. Overall, our best performing method achieves an F1-Score of 80.1%.
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