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深度学习自动评估荧光原位杂交图像中的 HER2 基因扩增状态。

Deep learning to automatically evaluate HER2 gene amplification status from fluorescence in situ hybridization images.

机构信息

Department of Pathology, Fudan University Shanghai Cancer Centre, 270 Dong'an Road, Shanghai, 200032, China.

Department of Oncology, Shanghai Medical College Fudan University, Shanghai, China.

出版信息

Sci Rep. 2023 Jun 16;13(1):9746. doi: 10.1038/s41598-023-36811-z.

Abstract

Human epidermal growth factor receptor 2 (HER2) gene amplification helps identify breast cancer patients who may respond to targeted anti-HER2 therapy. This study aims to develop an automated method for quantifying HER2 fluorescence in situ hybridization (FISH) signals and improve the working efficiency of pathologists. An Aitrox artificial intelligence (AI) model based on deep learning was constructed, and a comparison between the AI model and traditional manual counting was performed. In total, 918 FISH images from 320 consecutive invasive breast cancers were analysed and automatically classified into 5 groups according to the 2018 ASCO/CAP guidelines. The overall classification accuracy was 85.33% (157/184) with a mean average precision of 0.735. In Group 5, the most common group, the consistency was as high as 95.90% (117/122), while the consistency was low in the other groups due to the limited number of cases. The causes of this inconsistency, including clustered HER2 signals, coarse CEP17 signals and some section quality problems, were analysed. The developed AI model is a reliable tool for evaluating HER2 amplification statuses, especially for breast cancer in Group 5; additional cases from multiple centres could further improve the accuracy achieved for other groups.

摘要

人类表皮生长因子受体 2(HER2)基因扩增有助于确定可能对靶向抗 HER2 治疗有反应的乳腺癌患者。本研究旨在开发一种自动量化 HER2 荧光原位杂交(FISH)信号的方法,并提高病理学家的工作效率。构建了基于深度学习的 Aitrox 人工智能(AI)模型,并对 AI 模型与传统手动计数进行了比较。总共分析了 320 例连续浸润性乳腺癌的 918 个 FISH 图像,并根据 2018 年 ASCO/CAP 指南自动分为 5 组。整体分类准确率为 85.33%(157/184),平均精度为 0.735。在最常见的第 5 组中,一致性高达 95.90%(117/122),而其他组由于病例数量有限,一致性较低。分析了导致这种不一致的原因,包括簇状 HER2 信号、粗 CEP17 信号和一些切片质量问题。开发的 AI 模型是评估 HER2 扩增状态的可靠工具,特别是对于第 5 组的乳腺癌;来自多个中心的更多病例可以进一步提高其他组的准确性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8a62/10275857/1cd46f165f54/41598_2023_36811_Fig1_HTML.jpg

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