Department of Anatomical and Cellular Pathology, Prince of Wales Hospital, The Chinese University of Hong Kong, Hong Kong, Hong Kong.
Cancer Cytopathol. 2022 Jun;130(6):455-468. doi: 10.1002/cncy.22559. Epub 2022 Feb 25.
Fine-needle aspiration (FNA) is a robust diagnostic technique often used for tissue diagnosis of metastatic carcinoma. For interpretation of FNA cytology, cell block immunohistochemistry (IHC) and clinicocytologic parameters are indispensable. In this review of a large cohort, the current report: 1) describes clinicocytologic parameters and immunoprofiles of aspirates of metastatic carcinoma, 2) compares the predictivity of immunostains and classical approaches for IHC interpretation, and 3) describes machine learning-based algorithms for IHC interpretation.
Aspirates of metastatic carcinoma that had IHC performed were retrieved. Clinicocytologic parameters, IHC results, the corresponding primary site, and histologic diagnoses were recorded. By using machine learning, decision trees for predicting the primary site were generated, their performance was compared with 2 human-designed algorithms, and the primary site was suggested in the historical diagnosis.
In total, 1145 cases were identified. The 6 most populated groups were selected for machine learning and predictive analysis. With IHC input, the decision tree achieved a concordance rate of 94.5% and overall accuracy of 83.6%, which improved to 95.3% and 85.8%, respectively, when clinical data were incorporated and exceeded the human-designed IHC algorithms (P < .001). The historical diagnosis was more accurate unless indeterminate diagnoses were regarded as discordant (P < .001). CDX2 and TTF-1 immunostains had the highest weight in model accuracy, occupied the root of the decision trees, scored higher as features of importance, and outperformed the predictive power of cytokeratins 7 and 20.
Cytokeratins 7 and 20 may be superseded in immunostaining panels, including organ-specific immunostains such as CDX2 and TTF-1. Machine learning generates algorithms that surpasses human-designed algorithms but is inferior to expert assessment integrating clinical and cytologic assessment.
细针穿刺(FNA)是一种强大的诊断技术,常用于转移性癌的组织诊断。为了解释 FNA 细胞学,细胞块免疫组织化学(IHC)和临床细胞学参数是不可或缺的。在对大量队列的回顾中,本报告:1)描述了转移性癌抽吸物的临床细胞学参数和免疫表型,2)比较了免疫染色和 IHC 解释的经典方法的预测性,3)描述了基于机器学习的 IHC 解释算法。
检索了进行 IHC 的转移性癌抽吸物。记录了临床细胞学参数、免疫组化结果、相应的原发部位和组织学诊断。通过使用机器学习,为预测原发部位生成决策树,比较了其与 2 个人工设计算法的性能,并在历史诊断中提示了原发部位。
共确定了 1145 例。选择了 6 个最常见的组进行机器学习和预测分析。使用 IHC 输入,决策树的一致性率为 94.5%,总准确率为 83.6%,当纳入临床数据时,分别提高到 95.3%和 85.8%,超过了人工设计的 IHC 算法(P<0.001)。历史诊断更准确,除非将不确定诊断视为不一致(P<0.001)。CDX2 和 TTF-1 免疫染色在模型准确性方面具有最高权重,占据决策树的根,作为重要特征的得分更高,并且超过了细胞角蛋白 7 和 20 的预测能力。
细胞角蛋白 7 和 20 在免疫染色组中可能被取代,包括 CDX2 和 TTF-1 等器官特异性免疫染色。机器学习生成的算法优于人工设计的算法,但不如整合临床和细胞学评估的专家评估。