Kök Yunus Baran, Ekici Işın Doğan, İnce Ümit
Acıbadem University, Istanbul, Türkiye.
J Pathol Inform. 2025 May 16;18:100451. doi: 10.1016/j.jpi.2025.100451. eCollection 2025 Aug.
Calculation of tumor cell percentage, a critical pre-analytical component in molecular pathology, is typically performed by pathologists estimating a ratio. This semiquantitative approach can lead to inter-observer variability, potentially adversely affecting patient management and treatment outcomes. In era of digital pathology, it became crucial to automate such assessments for more objective approach. This study aims to contribute to this process by developing a model for automated calculation of tumor cell percentage in high-grade serous carcinomas. Tumor containing hematoxylin-eosin slides from 100 patients were divided into training, validation, and test groups. Slides were digitalized and placed in QuPath platform. Image patches were obtained from WSIs of training and validation sets, and were stitched together to form digital microarrays by using ImageJ extension. Subsequently, nuclear detection and segmentation were performed using StarDist software, and tumor and non-tumor cell nuclei were classified using annotations. For binary classifier, random forest algorithm was selected. With hyperparameter tuning, many pre-models were assessed by cross-validation and most suitable pre-model was selected to apply to test set. Testing was performed on WSIs and criterion standard was based on corresponding immunohistochemistry (p53 or PAX8) slides which showed diffuse positivitity for tumor cells. Performance of model was measured using regression metrics. This study is designed to perform and assess a classifier in whole slide images to reflect real-world experience.
肿瘤细胞百分比的计算是分子病理学中一个关键的分析前组成部分,通常由病理学家通过估计比例来进行。这种半定量方法可能导致观察者间的差异,潜在地对患者管理和治疗结果产生不利影响。在数字病理学时代,为了采用更客观的方法,自动化此类评估变得至关重要。本研究旨在通过开发一种用于自动计算高级别浆液性癌中肿瘤细胞百分比的模型,为这一过程做出贡献。来自100名患者的含有苏木精-伊红染色切片的肿瘤被分为训练组、验证组和测试组。切片进行数字化处理后放置在QuPath平台上。从训练集和验证集的全切片图像中获取图像块,并使用ImageJ扩展程序将它们拼接在一起形成数字微阵列。随后,使用StarDist软件进行细胞核检测和分割,并使用注释对肿瘤和非肿瘤细胞核进行分类。对于二分类器,选择了随机森林算法。通过超参数调整,通过交叉验证评估了许多预模型,并选择了最合适的预模型应用于测试集。在全切片图像上进行测试,标准基于显示肿瘤细胞弥漫阳性的相应免疫组织化学(p53或PAX8)切片。使用回归指标测量模型的性能。本研究旨在在全切片图像中执行和评估一个分类器,以反映实际经验。