Department of Pathology and Laboratory Medicine, University of Wisconsin School of Medicine and Public Health, Madison, WI, USA.
Department of Biostatistics and Data Science, Tulane University School of Public Health and Tropical Medicine, New Orleans, LA, USA.
Virchows Arch. 2022 Jul;481(1):49-61. doi: 10.1007/s00428-022-03311-w. Epub 2022 Apr 7.
Subtyping of hepatocellular adenoma (HCA) is an important task in practice as different subtypes may have different clinical outcomes and management algorithms. Definitive subtyping is currently dependent on immunohistochemical and molecular testing. The association between some morphologic/clinical features and HCA subtypes has been reported; however, the predictive performance of these features has been controversial. In this study, we attempted machine learning based methods to select an efficient and parsimonious set of morphologic/clinical features for differentiating a HCA subtype from the others, and then assessed the performance of the selected features in identifying the correct subtypes. We first examined 50 liver HCA resection specimens collected at the University of Washington and Kobe University/Kings College London, including HNF1α-mutated HCA (H-HCA) (n = 16), inflammatory HCA (I-HCA) (n = 20), beta-catenin activated HCA (β-HCA) (n = 8), and unclassified HCA (U-HCA) (n = 6). Twenty-six morphologic/clinical features were assessed. We used LASSO (least absolute shrinkage and selection operator) to select key features that could differentiate a subtype from the others. We further performed SVM (support vector machine) analysis to assess the performance (sensitivity, specificity, positive predictive value (PPV), negative predictive value (NPV), and accuracy) of the selected features in HCA subtyping in an independent cohort of liver resection samples (n = 20) collected at the University of Wisconsin-Madison. With some overlap, different combinations of morphologic/clinical features were selected for each subtype. Based on SVM analysis, the selected features classified HCA into correct subtypes with an overall accuracy of at least 80%. Our findings are useful for initial diagnosis and subtyping of HCA, especially in clinical settings without access to immunohistochemical and molecular assays.
肝细胞腺瘤 (HCA) 的亚型分类在实践中非常重要,因为不同的亚型可能具有不同的临床结局和管理方案。目前,明确的亚型分类依赖于免疫组织化学和分子检测。一些形态/临床特征与 HCA 亚型之间的相关性已经有报道;然而,这些特征的预测性能存在争议。在这项研究中,我们尝试使用基于机器学习的方法来选择一组高效且简约的形态/临床特征,用于区分 HCA 亚型,然后评估所选特征在识别正确亚型方面的性能。
我们首先检查了华盛顿大学和神户大学/伦敦国王学院收集的 50 例肝 HCA 切除标本,包括 HNF1α 突变型 HCA (H-HCA) (n=16)、炎症性 HCA (I-HCA) (n=20)、β-连环蛋白激活型 HCA (β-HCA) (n=8) 和未分类 HCA (U-HCA) (n=6)。评估了 26 种形态/临床特征。我们使用 LASSO(最小绝对收缩和选择算子)来选择可以区分亚型的关键特征。我们进一步进行 SVM(支持向量机)分析,以评估所选特征在麦迪逊威斯康星大学肝脏切除样本独立队列 (n=20) 中进行 HCA 亚型分类的性能 (敏感性、特异性、阳性预测值 (PPV)、阴性预测值 (NPV) 和准确性)。
虽然存在一些重叠,但不同的形态/临床特征组合被选择用于每种亚型。基于 SVM 分析,所选特征将 HCA 正确分类为至少 80%的正确亚型。我们的研究结果有助于 HCA 的初步诊断和亚型分类,特别是在没有免疫组织化学和分子检测的临床环境中。