Kurowski Konrad, Timme Sylvia, Föll Melanie Christine, Backhaus Clara, Holzner Philipp Anton, Bengsch Bertram, Schilling Oliver, Werner Martin, Bronsert Peter
Institute for Surgical Pathology, Medical Center, Faculty of Medicine, University of Freiburg, 79106 Freiburg, Germany.
Core Facility Histopathology and Digital Pathology Freiburg, Medical Center, University of Freiburg, 79106 Freiburg, Germany.
Methods Protoc. 2024 Nov 25;7(6):96. doi: 10.3390/mps7060096.
Immunohistochemical (IHC) studies of formalin-fixed paraffin-embedded (FFPE) samples are a gold standard in oncology for tumor characterization, and the identification of prognostic and predictive markers. However, despite the abundance of archived FFPE samples, their research use is limited due to the labor-intensive nature of IHC on large cohorts. This study aimed to create a high-throughput workflow using modern technologies to facilitate IHC biomarker studies on large patient groups. Semiautomatic constructed tissue microarrays (TMAs) were created for two tumor patient cohorts and IHC stained for seven antibodies (ABs). AB expression in the tumor and surrounding stroma was quantified using the AI-supported image analysis software QuPath. The data were correlated with clinicopathological information using an R-script, all results were automatically compiled into formatted reports. By minimizing labor time to 7.7%-compared to whole-slide studies-the established workflow significantly reduced human and material resource consumption. It successfully correlated AB expression with overall patient survival and additional clinicopathological data, providing publication-ready figures and tables. The AI-assisted high-throughput TMA workflow, validated on two patient cohorts, streamlines modern histopathological research by offering cost and time efficiency compared to traditional whole-slide studies. It maintains research quality and preserves patient tissue while significantly reducing material and human resources, making it ideal for high-throughput research centers and collaborations.
对福尔马林固定石蜡包埋(FFPE)样本进行免疫组织化学(IHC)研究是肿瘤学中用于肿瘤特征描述以及识别预后和预测标志物的金标准。然而,尽管有大量存档的FFPE样本,但由于对大型队列进行IHC研究需要耗费大量人力,其研究用途受到限制。本研究旨在利用现代技术创建一种高通量工作流程,以促进对大型患者群体进行IHC生物标志物研究。为两个肿瘤患者队列构建了半自动组织微阵列(TMA),并对七种抗体(AB)进行了IHC染色。使用人工智能支持的图像分析软件QuPath对肿瘤和周围基质中的AB表达进行定量。使用R脚本将数据与临床病理信息相关联,所有结果自动汇编成格式化报告。与全玻片研究相比,通过将人工时间减少到7.7%,所建立的工作流程显著减少了人力和物力消耗。它成功地将AB表达与患者总生存期及其他临床病理数据相关联,提供了可供发表的图表。在两个患者队列上得到验证的人工智能辅助高通量TMA工作流程,与传统的全玻片研究相比,通过提高成本和时间效率,简化了现代组织病理学研究。它在显著减少材料和人力资源的同时,保持了研究质量并保存了患者组织,使其成为高通量研究中心和合作项目的理想选择。