Yiping Jiao

Yiping Jiao, Jeroen van der Laak, Shadi Albarqouni et al. · eth-zurich

We introduce LYSTO, the Lymphocyte Assessment Hackathon, which was held in conjunction with the MICCAI 2019 Conference in Shenzen (China). The competition required participants to automatically assess the number of lymphocytes, in particular T-cells, in histopathological images of colon, breast, and prostate cancer stained with CD3 and CD8 immunohistochemistry. Differently from other challenges setup in medical image analysis, LYSTO participants were solely given a few hours to address this problem. In this paper, we describe the goal and the multi-phase organization of the hackathon; we describe the proposed methods and the on-site results. Additionally, we present post-competition results where we show how the presented methods perform on an independent set of lung cancer slides, which was not part of the initial competition, as well as a comparison on lymphocyte assessment between presented methods and a panel of pathologists. We show that some of the participants were capable to achieve pathologist-level performance at lymphocyte assessment. After the hackathon, LYSTO was left as a lightweight plug-and-play benchmark dataset on grand-challenge website, together with an automatic evaluation platform. LYSTO has supported a number of research in lymphocyte assessment in oncology. LYSTO will be a long-lasting educational challenge for deep learning and digital pathology, it is available at https://lysto.grand-challenge.org/.

Abu Bakor Hayat Arnob, Xiangxue Wang, Yiping Jiao et al.

Medical image processing usually requires a model trained with carefully crafted datasets due to unique image characteristics and domain-specific challenges, especially in pathology. Primitive detection and segmentation in digitized tissue samples are essential for objective and automated diagnosis and prognosis of cancer. SAM (Segment Anything Model) has recently been developed to segment general objects from natural images with high accuracy, but it requires human prompts to generate masks. In this work, we present a novel approach that adapts pre-trained natural image encoders of SAM for detection-based region proposals. Regions proposed by a pre-trained encoder are sent to cascaded feature propagation layers for projection. Then, local semantic and global context is aggregated from multi-scale for bounding box localization and classification. Finally, the SAM decoder uses the identified bounding boxes as essential prompts to generate a comprehensive primitive segmentation map. The entire base framework, SAM, requires no additional training or fine-tuning but could produce an end-to-end result for two fundamental segmentation tasks in pathology. Our method compares with state-of-the-art models in F1 score for nuclei detection and binary/multiclass panoptic(bPQ/mPQ) and mask quality(dice) for segmentation quality on the PanNuke dataset while offering end-to-end efficiency. Our model also achieves remarkable Average Precision (+4.5%) on the secondary dataset (HuBMAP Kidney) compared to Faster RCNN. The code is publicly available at https://github.com/learner-codec/autoprom_sam.

Anwen Lu, Mingxin Liu, Yiping Jiao et al.

Primary liver malignancies are widely recognized as the most heterogeneous and prognostically diverse cancers of the digestive system. Among these, hepatocellular carcinoma (HCC) and intrahepatic cholangiocarcinoma (ICC) emerge as the two principal histological subtypes, demonstrating significantly greater complexity in tissue morphology and cellular architecture than other common tumors. The intricate representation of features in Whole Slide Images (WSIs) encompasses abundant crucial information for liver cancer histological subtyping, regarding hierarchical pyramid structure, tumor microenvironment (TME), and geometric representation. However, recent approaches have not adequately exploited these indispensable effective descriptors, resulting in a limited understanding of histological representation and suboptimal subtyping performance. To mitigate these limitations, ARGUS is proposed to advance histological subtyping in liver cancer by capturing the macro-meso-micro hierarchical information within the TME. Specifically, we first construct a micro-geometry feature to represent fine-grained cell-level pattern via a geometric structure across nuclei, thereby providing a more refined and precise perspective for delineating pathological images. Then, a Hierarchical Field-of-Views (FoVs) Alignment module is designed to model macro- and meso-level hierarchical interactions inherent in WSIs. Finally, the augmented micro-geometry and FoVs features are fused into a joint representation via present Geometry Prior Guided Fusion strategy for modeling holistic phenotype interactions. Extensive experiments on public and private cohorts demonstrate that our ARGUS achieves state-of-the-art (SOTA) performance in histological subtyping of liver cancer, which provide an effective diagnostic tool for primary liver malignancies in clinical practice.