Alessandro Ferrero

Bodong Zhang, Beatrice Knudsen, Deepika Sirohi et al.

We propose a novel semi-supervised learning approach for classification of histopathology images. We employ strong supervision with patch-level annotations combined with a novel co-training loss to create a semi-supervised learning framework. Co-training relies on multiple conditionally independent and sufficient views of the data. We separate the hematoxylin and eosin channels in pathology images using color deconvolution to create two views of each slide that can partially fulfill these requirements. Two separate CNNs are used to embed the two views into a joint feature space. We use a contrastive loss between the views in this feature space to implement co-training. We evaluate our approach in clear cell renal cell and prostate carcinomas, and demonstrate improvement over state-of-the-art semi-supervised learning methods.

Alessandro Ferrero, Beatrice Knudsen, Deepika Sirohi et al.

Pathologists diagnose and grade prostate cancer by examining tissue from needle biopsies on glass slides. The cancer's severity and risk of metastasis are determined by the Gleason grade, a score based on the organization and morphology of prostate cancer glands. For diagnostic work-up, pathologists first locate glands in the whole biopsy core, and -- if they detect cancer -- they assign a Gleason grade. This time-consuming process is subject to errors and significant inter-observer variability, despite strict diagnostic criteria. This paper proposes an automated workflow that follows pathologists' \textit{modus operandi}, isolating and classifying multi-scale patches of individual glands in whole slide images (WSI) of biopsy tissues using distinct steps: (1) two fully convolutional networks segment epithelium versus stroma and gland boundaries, respectively; (2) a classifier network separates benign from cancer glands at high magnification; and (3) an additional classifier predicts the grade of each cancer gland at low magnification. Altogether, this process provides a gland-specific approach for prostate cancer grading that we compare against other machine-learning-based grading methods.

Alessandro Ferrero, Shireen Elhabian, Ross Whitaker

Generative adversarial networks (GANs) have proven effective in modeling distributions of high-dimensional data. However, their training instability is a well-known hindrance to convergence, which results in practical challenges in their applications to novel data. Furthermore, even when convergence is reached, GANs can be affected by mode collapse, a phenomenon for which the generator learns to model only a small part of the target distribution, disregarding the vast majority of the data manifold or distribution. This paper addresses these challenges by introducing SetGAN, an adversarial architecture that processes sets of generated and real samples, and discriminates between the origins of these sets (i.e., training versus generated data) in a flexible, permutation invariant manner. We also propose a new metric to quantitatively evaluate GANs that does not require previous knowledge of the application, apart from the data itself. Using the new metric, in conjunction with the state-of-the-art evaluation methods, we show that the proposed architecture, when compared with GAN variants stemming from similar strategies, produces more accurate models of the input data in a way that is also less sensitive to hyperparameter settings.