Xu Jing, Shi Lei, Li Shuxi, Zhang Yameng, Zhao Guohua, Shi Yucheng, Li Jie, Gao Yufei
IEEE Trans Image Process. 2025;34:2883-2895. doi: 10.1109/TIP.2025.3565184. Epub 2025 May 9.
Automatic nuclei segmentation and classification (NSC) is a fundamental prerequisite in digital pathology analysis as it enables the quantification of biomarkers and histopathological features for precision medicine. Nuclei appear to be small, however, global spatial distribution and brightness contrast, or color correlation between the nucleus and background, have been recognized as key rationales for accurate nuclei segmentation in actual clinical practice. Although recent great breakthroughs in medical image segmentation have been achieved by Transformer-based methods, the adaptability of segmenting and classifying nuclei from histopathological images is rarely investigated. Also, the severe overlap of nuclei and the large intra-class variability are common in clinical wild data. Prevailing methods based on polygonal representations or distance maps are limited by empirically designed post-processing strategies, resulting in ineffective segmentation of large irregular nuclei instances. To address these challenges, we propose a keypoint-guided tri-decoder Transformer (PointFormer) for NSC simultaneously. Specifically, the overall NSC task is decoupled to a multi-task learning problem, where a tri-decoder structure is employed for decoding nuclei instance, edges, and types, respectively. The nuclei detection and classification (NDC) subtask is reformulated as a semantic keypoint estimation problem. Meanwhile, introduces a novel attention-guiding strategy to capture strong inter-branch correlations and mitigate inconsistencies between multi-decoder predictions. Finally, a multi-local perception module is designed as the base building block of PointFormer to achieve local and global trade-offs and reduce model complexity. Comprehensive quantitative and qualitative experimental results on three datasets of different volumes have demonstrated the superiority of the proposed method over prevalent methods, especially for the PanNuke dataset with an achievement of 70.6% on bPQ.
自动细胞核分割与分类(NSC)是数字病理学分析的基本前提,因为它能够对生物标志物和组织病理学特征进行量化,以实现精准医学。细胞核看起来很小,然而,全局空间分布和亮度对比度,或者细胞核与背景之间的颜色相关性,已被认为是实际临床实践中准确细胞核分割的关键依据。尽管基于Transformer的方法在医学图像分割方面最近取得了重大突破,但从组织病理学图像中分割和分类细胞核的适应性很少被研究。此外,细胞核的严重重叠和较大的类内变异性在临床野生数据中很常见。基于多边形表示或距离图的现有方法受到经验设计的后处理策略的限制,导致对大型不规则细胞核实例的分割无效。为了应对这些挑战,我们同时提出了一种用于NSC的关键点引导三解码器Transformer(PointFormer)。具体来说,整体NSC任务被解耦为一个多任务学习问题,其中采用三解码器结构分别对细胞核实例、边缘和类型进行解码。细胞核检测与分类(NDC)子任务被重新表述为一个语义关键点估计问题。同时,引入了一种新颖的注意力引导策略,以捕获强分支间相关性并减轻多解码器预测之间的不一致性。最后,设计了一个多局部感知模块作为PointFormer的基本构建块,以实现局部和全局的权衡并降低模型复杂性。在三个不同规模的数据集上进行的全面定量和定性实验结果表明,所提出的方法优于现有方法,特别是对于PanNuke数据集,在bPQ上达到了70.6%的成绩。