College of Biomedical Engineering, Sichuan University, Chengdu 610065, China; College of Computer Science, Sichuan University, Chengdu 610065, China.
Tencent AI Lab, Shenzhen 518057, China.
Med Image Anal. 2023 Feb;84:102703. doi: 10.1016/j.media.2022.102703. Epub 2022 Nov 23.
Mitosis counting of biopsies is an important biomarker for breast cancer patients, which supports disease prognostication and treatment planning. Developing a robust mitotic cell detection model is highly challenging due to its complex growth pattern and high similarities with non-mitotic cells. Most mitosis detection algorithms have poor generalizability across image domains and lack reproducibility and validation in multicenter settings. To overcome these issues, we propose a generalizable and robust mitosis detection algorithm (called FMDet), which is independently tested on multicenter breast histopathological images. To capture more refined morphological features of cells, we convert the object detection task as a semantic segmentation problem. The pixel-level annotations for mitotic nuclei are obtained by taking the intersection of the masks generated from a well-trained nuclear segmentation model and the bounding boxes provided by the MIDOG 2021 challenge. In our segmentation framework, a robust feature extractor is developed to capture the appearance variations of mitotic cells, which is constructed by integrating a channel-wise multi-scale attention mechanism into a fully convolutional network structure. Benefiting from the fact that the changes in the low-level spectrum do not affect the high-level semantic perception, we employ a Fourier-based data augmentation method to reduce domain discrepancies by exchanging the low-frequency spectrum between two domains. Our FMDet algorithm has been tested in the MIDOG 2021 challenge and ranked first place. Further, our algorithm is also externally validated on four independent datasets for mitosis detection, which exhibits state-of-the-art performance in comparison with previously published results. These results demonstrate that our algorithm has the potential to be deployed as an assistant decision support tool in clinical practice. Our code has been released at https://github.com/Xiyue-Wang/1st-in-MICCAI-MIDOG-2021-challenge.
活检的有丝分裂计数是乳腺癌患者的一个重要生物标志物,支持疾病预后和治疗计划。由于其复杂的生长模式和与非有丝分裂细胞的高度相似性,开发一个强大的有丝分裂细胞检测模型极具挑战性。大多数有丝分裂检测算法在图像域之间的通用性较差,并且在多中心环境中缺乏可重复性和验证。为了克服这些问题,我们提出了一种通用且强大的有丝分裂检测算法(称为 FMDet),该算法在多中心乳腺组织病理学图像上进行了独立测试。为了捕获更精细的细胞形态特征,我们将目标检测任务转换为语义分割问题。有丝分裂核的像素级注释是通过取核分割模型生成的掩模与 MIDOG 2021 挑战赛提供的边界框的交集获得的。在我们的分割框架中,开发了一种强大的特征提取器来捕获有丝分裂细胞的外观变化,该特征提取器通过将通道式多尺度注意力机制集成到全卷积网络结构中构建而成。由于低频谱的变化不会影响高层语义感知,因此我们采用基于傅里叶的增强方法通过在两个域之间交换低频谱来减少域差异。我们的 FMDet 算法已在 MIDOG 2021 挑战赛中进行了测试,并排名第一。此外,我们的算法还在四个独立的有丝分裂检测数据集上进行了外部验证,与之前发表的结果相比,表现出了最先进的性能。这些结果表明,我们的算法有可能被部署为临床实践中的辅助决策支持工具。我们的代码已在 https://github.com/Xiyue-Wang/1st-in-MICCAI-MIDOG-2021-challenge 上发布。