arXiv:2511.08896cs.CVcs.AI2025-11

用EfficientNet自动识别胶质母细胞瘤六类组织区域,助力病理诊断

Classifying Histopathologic Glioblastoma Sub-regions with EfficientNet

  • 基于EfficientNet构建四步深度学习流程,实现六类肿瘤区域分类
  • 在训练集上达0.98的F1分数,验证集和测试集分别为0.546和0.517
  • 为临床病理分析提供可扩展的自动化工具,适合医学图像研究者参考

胶质母细胞瘤(GBM)是最常见且进展迅速的脑肿瘤,预后极差。尽管临床诊断技术不断进步,患者生存率仍未显著改善。组织病理学评估是肿瘤切除后的常规诊断方法。我们提出,通过自动化、稳健且准确地识别GBM内不同组织亚区,可实现对疾病形态学特征的大规模理解。本研究设计了一种四步深度学习方法,用于分类六个(6)类组织区域,并在BraTS-Path 2024挑战赛数据集上进行定量评估。该数据集包含经苏木精-伊红(H&E)染色的数字化GBM组织切片,标注了六种不同区域。我们使用挑战赛公开的训练数据集,开发并评估了多种EfficientNet架构(B0、B1、B2、B3、B4)的变体。其中EfficientNet-B1与EfficientNet-B4表现最佳,在五折交叉验证中取得0.98的F1分数。在独立验证集和最终测试集上的性能分别为0.546和0.517。模型在训练、验证与测试数据上的性能差异,凸显其泛化能力的挑战,这对临床应用至关重要。代码已开源:https://github.com/IUCompPath/brats-path-2024-enet。

原文摘要 · Abstract (English)

Glioblastoma (GBM) is the most common aggressive, fast-growing brain tumor, with a grim prognosis. Despite clinical diagnostic advancements, there have not been any substantial improvements to patient prognosis. Histopathological assessment of excised tumors is the first line of clinical diagnostic routine. We hypothesize that automated, robust, and accurate identification of distinct histological sub-regions within GBM could contribute to morphologically understanding this disease at scale. In this study, we designed a four-step deep learning approach to classify six (6) histopathological regions and quantitatively evaluated it on the BraTS-Path 2024 challenge dataset, which includes digitized Hematoxylin \& Eosin (H\&E) stained GBM tissue sections annotated for six distinct regions. We used the challenge's publicly available training dataset to develop and evaluate the effectiveness of several variants of EfficientNet architectures (i.e., B0, B1, B2, B3, B4). EfficientNet-B1 and EfficientNet-B4 achieved the best performance, achieving an F1 score of 0.98 in a 5-fold cross-validation configuration using the BraTS-Path training set. The quantitative performance evaluation of our proposed approach with EfficientNet-B1 on the BraTS-Path hold-out validation data and the final hidden testing data yielded F1 scores of 0.546 and 0.517, respectively, for the associated 6-class classification task. The difference in the performance on training, validation, and testing data highlights the challenge of developing models that generalize well to new data, which is crucial for clinical applications. The source code of the proposed approach can be found at the GitHub repository of Indiana University Division of Computational Pathology: https://github.com/IUCompPath/brats-path-2024-enet.

病理图像EfficientNet分类医学影像

Thank you to arXiv for use of its open access interoperability. PaperDance 不是 arXiv 官方产品;中文卡片由大模型生成,请以原文为准。