Mr. Kyle S. Gerard Profile

Kyle S. Gerard

at EPFL

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Proceedings Article | 15 February 2021 Presentation + Paper

A multi-scale conditional deep model for tumor cell ratio counting

Eric Cosatto, Kyle Gerard, Hans-Peter Graf, Maki Ogura, Tomoharu Kiyuna, Kanako Hatanaka, Yoshihiro Matsuno, Yutaka Hatanaka

Proceedings Volume 11603, 1160308 (2021) https://doi.org/10.1117/12.2581108

KEYWORDS: Tumors, Tissues, Data modeling, Zoom lenses, Parallel computing, Lung, Genomics, Convolutional neural networks

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We propose a method to accurately obtain the ratio of tumor cells over an entire histological slide. We use deep fully convolutional neural network models trained to detect and classify cells on images of H&E-stained tissue sections. Pathologists' labels consisting of exhaustive nuclei locations and tumor regions were used to trained the model in a supervised fashion. We show that combining two models, each working at a different magnification allows the system to capture both cell-level details and surrounding context to enable successful detection and classification of cells as either tumor-cell or normal-cell. Indeed, by conditioning the classification of a single cell on a multi-scale context information, our models mimic the process used by pathologists who assess cell neoplasticity and tumor extent at different microscope magnifications. The ratio of tumor cells can then be readily obtained by counting the number of cells in each class. To analyze an entire slide, we split it into multiple tiles that can be processed in parallel. The overall tumor cell ratio can then be aggregated. We perform experiments on a dataset of 100 slides with lung tumor specimens from both resection and tissue micro-array (TMA). We train fully-convolutional models using heavy data augmentation and batch normalization. On an unseen test set, we obtain an average mean absolute error on predicting the tumor cell ratio of less than 6%, which is significantly better than the human average of 20% and is key in properly selecting tissue samples for recent genetic panel tests geared at prescribing targeted cancer drugs. We perform ablation studies to show the importance of training two models at different magnifications and to justify the choice of some parameters, such as the size of the receptive field.

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