分割
多发性骨髓瘤
计算机科学
聚类分析
人工智能
细胞质
图像分割
等离子体电池
像素
模式识别(心理学)
病理
计算机视觉
医学
生物
免疫学
细胞生物学
作者
Anubha Gupta,Shiv Gehlot,Shubham Goswami,Sachin Motwani,Ritu Gupta,Álvaro García Faura,Dejan Štepec,Tomaž Martinčič,Reza Azad,Dorit Merhof,Afshin Bozorgpour,Babak Azad,Alaa Sulaiman,Deepanshu Pandey,Pradyumna Gupta,Sumit Bhattacharya,Aman Sinha,Rohit Agarwal,Xinyun Qiu,Yucheng Zhang
标识
DOI:10.1016/j.media.2022.102677
摘要
Multiple Myeloma (MM) is an emerging ailment of global concern. Its diagnosis at the early stages is critical for recovery. Therefore, efforts are underway to produce digital pathology tools with human-level intelligence that are efficient, scalable, accessible, and cost-effective. Following the trend, a medical imaging challenge on “Segmentation of Multiple Myeloma Plasma Cells in Microscopic Images (SegPC-2021)” was organized at the IEEE International Symposium on Biomedical Imaging (ISBI), 2021, France. The challenge addressed the problem of cell segmentation in microscopic images captured from the slides prepared from the bone marrow aspirate of patients diagnosed with Multiple Myeloma. The challenge released a total of 775 images with 690 and 85 images of sizes 2040×1536 and 1920×2560 pixels, respectively, captured from two different (microscope and camera) setups. The participants had to segment the plasma cells with a separate label on each cell’s nucleus and cytoplasm. This problem comprises many challenges, including a reduced color contrast between the cytoplasm and the background, and the clustering of cells with a feeble boundary separation of individual cells. To our knowledge, the SegPC-2021 challenge dataset is the largest publicly available annotated data on plasma cell segmentation in MM so far. The challenge targets a semi-automated tool to ensure the supervision of medical experts. It was conducted for a span of five months, from November 2020 to April 2021. Initially, the data was shared with 696 people from 52 teams, of which 41 teams submitted the results of their models on the evaluation portal in the validation phase. Similarly, 20 teams qualified for the last round, of which 16 teams submitted the results in the final test phase. All the top-5 teams employed DL-based approaches, and the best mIoU obtained on the final test set of 277 microscopic images was 0.9389. All these five models have been analyzed and discussed in detail. This challenge task is a step towards the target of creating an automated MM diagnostic tool.
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