Haeyoun Kang, Yujin Nam, Dat Ngo, Min-Sun Cho, Wonae Lee, Hyeong-Chan Shin, Yujun Park, Hee Jung An, Hee-Cheol Kim, Nam Hoon Cho, Hyunki Kim, Baek Hwan Cho
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Abstract
Epstein–Barr virus associated gastric carcinoma (EBVaGC) represents a distinct molecular subtype of gastric cancer with prognostic and therapeutic significance. Current diagnostic practice relies on Epstein-Barr virus-encoded small RNA (EBER) in situ hybridization, which is rarely performed on initial biopsy specimens. We developed a deep learning-based diagnostic pipeline that predicts EBV status directly from H&E-stained gastric biopsy slides. Our method incorporates a multiple bag instance learning (MBIL) framework, which groups spatially adjacent tumor patches to address the inherent heterogeneity of biopsy samples and improve predictive performance. A pathology foundation model was employed to distinguish tumor from normal regions with minimal pathologist annotation, enabling robust tumor detection and contributing to downstream model accuracy. The model was trained on 744 biopsy cases from three general hospitals using 5-fold cross-validation and evaluated on an independent external cohort of 157 cases. MBIL-based models consistently outperformed single-bag approaches. The DSMIL-MB model achieved the best performance, with an area under the receiver operating characteristic curve (AUC) of 0.907 ± 0.044 in internal validation and 0.870 in external testing. TransMIL also showed improved performance with MBIL, with external AUC increasing from 0.701 to 0.853. This framework may serve as a practical prescreening tool for EBV status prediction in routine gastric biopsy specimens prior to EBER-ISH testing, supporting preoperative decision-making and facilitating broader implementation of EBV screening in gastric cancer diagnostics. © 2026 The Pathological Society of Great Britain and Ireland.
基于多袋实例学习和多中心数据基础模型的胃癌活检图像EBV状态预测。
Epstein-Barr病毒相关性胃癌(EBVaGC)是一种独特的胃癌分子亚型,具有预后和治疗意义。目前的诊断实践依赖于爱泼斯坦-巴尔病毒编码的小RNA (EBER)原位杂交,这种方法很少用于初始活检标本。我们开发了一种基于深度学习的诊断管道,可以直接从h&e染色的胃活检切片中预测EBV状态。我们的方法结合了一个多袋实例学习(MBIL)框架,该框架将空间上相邻的肿瘤斑块分组,以解决活检样本的内在异质性,提高预测性能。采用病理学基础模型以最小的病理学注释区分肿瘤和正常区域,从而实现鲁棒的肿瘤检测并有助于下游模型的准确性。该模型在三家综合医院的744例活检病例中进行了训练,使用5倍交叉验证,并在157例独立的外部队列中进行了评估。基于mbl的模型始终优于单包方法。DSMIL-MB模型表现最佳,内部验证的受试者工作特征曲线下面积(AUC)为0.907±0.044,外部测试的AUC为0.870。TransMIL与MBIL的性能也有所提高,外部AUC从0.701提高到0.853。该框架可作为EBER-ISH检测前常规胃活检标本中EBV状态预测的实用预筛查工具,支持术前决策,促进EBV筛查在胃癌诊断中的更广泛实施。©2026英国和爱尔兰病理学会。
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