提出可旋转不变的组织病理学特征,提升无监督分割鲁棒性
Equivariant Imaging Biomarkers for Robust Unsupervised Segmentation of Histopathology
- 设计对称卷积核,使模型对旋转/翻转保持等变性
- 在50例前列腺组织微阵列数据上验证,旋转下分割性能更稳定
- 适合追求模型泛化能力的数字病理研究者
通过显微镜检查组织样本进行病理评估对准确诊断和预后至关重要。然而,传统由专业病理科医生进行的手动分析耗时、费力、成本高且存在评分者间差异,可能影响诊断的一致性和准确性。随着数字病理图像数量激增,自动化分析迫在眉睫。近年来,基于人工智能的机器学习(ML)模型显著提升了组织切片分析的精度与效率。但现有模型仅对平移保持不变性,缺乏对旋转和翻转的不变性,限制了其在组织病理学中的泛化能力,因图像本身无明确方向。本研究通过无监督分割,开发出基于新型对称卷积核的鲁棒等变组织病理学生物标志物。在来自50名患者的前列腺组织微阵列(TMA)图像上,使用Gleason 2019挑战赛公开数据集进行验证。相比使用标准卷积核的模型,该方法提取的生物标志物在旋转条件下展现出更强的鲁棒性和泛化能力,有望提升机器学习模型在数字病理中诊断与预后的准确性、一致性和鲁棒性。最终,该工作旨在将等变成像应用于超越前列腺癌的更广泛病理诊断与预后场景。
原文摘要 · Abstract (English)
Histopathology evaluation of tissue specimens through microscopic examination is essential for accurate disease diagnosis and prognosis. However, traditional manual analysis by specially trained pathologists is time-consuming, labor-intensive, cost-inefficient, and prone to inter-rater variability, potentially affecting diagnostic consistency and accuracy. As digital pathology images continue to proliferate, there is a pressing need for automated analysis to address these challenges. Recent advancements in artificial intelligence-based tools such as machine learning (ML) models, have significantly enhanced the precision and efficiency of analyzing histopathological slides. However, despite their impressive performance, ML models are invariant only to translation, lacking invariance to rotation and reflection. This limitation restricts their ability to generalize effectively, particularly in histopathology, where images intrinsically lack meaningful orientation. In this study, we develop robust, equivariant histopathological biomarkers through a novel symmetric convolutional kernel via unsupervised segmentation. The approach is validated using prostate tissue micro-array (TMA) images from 50 patients in the Gleason 2019 Challenge public dataset. The biomarkers extracted through this approach demonstrate enhanced robustness and generalizability against rotation compared to models using standard convolution kernels, holding promise for enhancing the accuracy, consistency, and robustness of ML models in digital pathology. Ultimately, this work aims to improve diagnostic and prognostic capabilities of histopathology beyond prostate cancer through equivariant imaging.
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