Mitosis detection is one of the challenging problems in computational pathology, and mitotic count is an important index of cancer grading for pathologists. However, current counts of mitotic nuclei rely on pathologists looking microscopically at the number of mitotic nuclei in hot spots, which is subjective and time-consuming. In this paper, we propose a two-stage cascaded network, named FoCasNet, for mitosis detection. In the first stage, a detection network named M_det is proposed to detect as many mitoses as possible. In the second stage, a classification network M_class is proposed to refine the results of the first stage. In addition, the attention mechanism, normalization method, and hybrid anchor branch classification subnet are introduced to improve the overall detection performance. Our method achieves the current highest F1-score of 0.888 on the public dataset ICPR 2012. We also evaluated our method on the GZMH dataset released by our research team for the first time and reached the highest F1-score of 0.563, which is also better than multiple classic detection networks widely used at present. It confirmed the effectiveness and generalization of our method. The code will be available at: https://github.com/antifen/mitosis-nuclei-detection.
翻译:在计算病理学方面,检测寄生虫病症是一个具有挑战性的问题,而线性计数是病理学家癌症分级的重要指数之一。然而,目前对线性核的计数取决于病理学家对热点中的线性核数量进行微观观察,这是主观和耗时的热点点中微核的数量。在本文中,我们建议建立一个名为FoCasNet的两阶段级级联网络,用于检测寄生虫病。在第一阶段,建议建立一个名为M_det的检测网络,以探测尽可能多的线性细胞。在第二阶段,建议建立一个分类网络M_类,以完善第一阶段的结果。此外,还引入关注机制、正常化方法和混合锚性锚分级分类子网,以提高总体检测性能。我们的方法达到了目前公共数据集的0.888个最高F-核心。2012年,我们还评估了我们研究小组首次发布的GZM-H数据集的方法,并达到了0.563的F1-核心,这也比多种经典检测网络要好。在目前普遍使用的方法中,它将使用。