人工智能分析仪对乳腺癌中 HER2、ER 和 PR 的增强解读:通过对 201 个病例的读者研究提高观察者之间的一致性。

IF 7.4 1区 医学 Q1 Medicine
Minsun Jung, Seung Geun Song, Soo Ick Cho, Sangwon Shin, Taebum Lee, Wonkyung Jung, Hajin Lee, Jiyoung Park, Sanghoon Song, Gahee Park, Heon Song, Seonwook Park, Jinhee Lee, Mingu Kang, Jongchan Park, Sergio Pereira, Donggeun Yoo, Keunhyung Chung, Siraj M Ali, So-Woon Kim
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引用次数: 0

摘要

背景:乳腺癌分子亚型的准确分类对于确定治疗策略和预测临床结果至关重要。这种分类在很大程度上取决于对人类表皮生长因子受体 2(HER2)、雌激素受体(ER)和孕激素受体(PR)状态的评估。然而,病理学家之间在解释上的差异给这一分类的准确性带来了挑战。本研究评估了人工智能(AI)在提高这些评估一致性方面的作用:方法:使用 1,259 张 HER2、744 张 ER 和 466 张 PR 染色的乳腺癌全切片免疫组化(IHC)图像,开发了由细胞和组织模型组成的人工智能驱动的 HER2 和 ER/PR 分析仪。使用这些人工智能分析仪分析了由 201 例乳腺癌病例的 HER2、ER 和 PR IHC 组成的外部验证队列。三位获得认证的病理学家在没有人工智能注释的情况下独立评估了这些病例。然后,病理学家与人工智能分析仪之间存在不同解释的病例在人工智能的协助下进行了重新评估,重点是评估与初始评估相比,人工智能的协助对病理学家在修订评估期间的一致性的影响:病理学家需要重新评估的 HER2 例数分别为 61 例(30.3%)、42 例(20.9%)和 80 例(39.8%),ER 例数分别为 15 例(7.5%)、17 例(8.5%)和 11 例(5.5%),PR 例数分别为 26 例(12.9%)、24 例(11.9%)和 28 例(13.9%)。与最初的解释相比,在人工智能的协助下,三位病理学家对 HER2 状态的一致意见明显增加(从 49.3% 增加到 74.1%,p 结论):本研究强调了人工智能分析仪在提高病理学家对乳腺癌分子亚型分类的一致性方面的重要作用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Augmented interpretation of HER2, ER, and PR in breast cancer by artificial intelligence analyzer: enhancing interobserver agreement through a reader study of 201 cases.

Background: Accurate classification of breast cancer molecular subtypes is crucial in determining treatment strategies and predicting clinical outcomes. This classification largely depends on the assessment of human epidermal growth factor receptor 2 (HER2), estrogen receptor (ER), and progesterone receptor (PR) status. However, variability in interpretation among pathologists pose challenges to the accuracy of this classification. This study evaluates the role of artificial intelligence (AI) in enhancing the consistency of these evaluations.

Methods: AI-powered HER2 and ER/PR analyzers, consisting of cell and tissue models, were developed using 1,259 HER2, 744 ER, and 466 PR-stained immunohistochemistry (IHC) whole-slide images of breast cancer. External validation cohort comprising HER2, ER, and PR IHCs of 201 breast cancer cases were analyzed with these AI-powered analyzers. Three board-certified pathologists independently assessed these cases without AI annotation. Then, cases with differing interpretations between pathologists and the AI analyzer were revisited with AI assistance, focusing on evaluating the influence of AI assistance on the concordance among pathologists during the revised evaluation compared to the initial assessment.

Results: Reevaluation was required in 61 (30.3%), 42 (20.9%), and 80 (39.8%) of HER2, in 15 (7.5%), 17 (8.5%), and 11 (5.5%) of ER, and in 26 (12.9%), 24 (11.9%), and 28 (13.9%) of PR evaluations by the pathologists, respectively. Compared to initial interpretations, the assistance of AI led to a notable increase in the agreement among three pathologists on the status of HER2 (from 49.3 to 74.1%, p < 0.001), ER (from 93.0 to 96.5%, p = 0.096), and PR (from 84.6 to 91.5%, p = 0.006). This improvement was especially evident in cases of HER2 2+ and 1+, where the concordance significantly increased from 46.2 to 68.4% and from 26.5 to 70.7%, respectively. Consequently, a refinement in the classification of breast cancer molecular subtypes (from 58.2 to 78.6%, p < 0.001) was achieved with AI assistance.

Conclusions: This study underscores the significant role of AI analyzers in improving pathologists' concordance in the classification of breast cancer molecular subtypes.

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来源期刊
CiteScore
12.00
自引率
0.00%
发文量
76
审稿时长
12 weeks
期刊介绍: Breast Cancer Research, an international, peer-reviewed online journal, publishes original research, reviews, editorials, and reports. It features open-access research articles of exceptional interest across all areas of biology and medicine relevant to breast cancer. This includes normal mammary gland biology, with a special emphasis on the genetic, biochemical, and cellular basis of breast cancer. In addition to basic research, the journal covers preclinical, translational, and clinical studies with a biological basis, including Phase I and Phase II trials.
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