Oncotype-DX HER2 单基因评分与免疫组化评估 HER2 低表达乳腺癌中 HER2 表达的关系

George Douganiotis, Loukas Kontovinis, Thomas Zarampoukas, Ioannis Natsiopoulos, Konstantinos Papazisis
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摘要

背景/目的:"HER2-低 "是一种新兴的乳腺癌亚型,有文献记载它在预测新型抗体药物共轭物治疗反应方面的作用。它是根据免疫组化方法定义的,但越来越多的证据表明,由于观察者之间的差异和方法本身的局限性,这种方法并不适合用于识别HER2-低亚群:我们回顾性分析了本部门数据库中430名接受过Oncotype-DX评分的患者数据,并评估了Oncotype-DX HER2单基因评分与免疫组化HER2表达的相关性。同时还评估了HER2-0亚组与HER2-低亚组的Oncotype-DX复发评分:结果:研究发现,HER2单基因评分与免疫组化的HER2结果准确相关,HER2-0与HER2+1肿瘤之间的差异具有统计学意义(p结论:HER2-0与HER2+1肿瘤之间的差异具有统计学意义(p结论:HER2-0与HER2+1肿瘤之间的差异具有统计学意义(p结论):与免疫组化相比,Oncotype-DX 的 HER2 单基因评分具有更好的可重复性和更小的观察者间差异,是评估精确 HER2 状态的潜在替代标记物。使用 rt-PCR 是评估 HER2 低亚组的另一种方法。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Association of Oncotype-DX HER2 Single Gene Score With HER2 Expression Assessed by Immunohistochemistry in HER2-low Breast Cancer.

Background/aim: "HER2-low" is an emerging subtype of breast cancer, with a documented role in predicting response to treatment with novel antibody-drug conjugates. It is defined based on immunohistochemistry, but increasing evidence is challenging this approach as appropriate for identifying the HER2-low subgroup, due to both interobserver variability and limitations of the method itself.

Patients and methods: We retrospectively analyzed data from 430 patients from our departmental databases who had been subjected to an Oncotype-DX score and assessed the correlation of the Oncotype-DX HER2 single-gene score with the HER2 expression on immunohistochemistry. The Oncotype-DX Recurrence Score was also evaluated in the HER2-0 versus HER2-low subgroups.

Results: The HER2 single-gene score was found to accurately correlate with the HER2 result on immunohistochemistry, with a statistically significant difference both between HER2-0 and HER2 +1 tumors (p<0.0001), as well as between HER2 +1 and +2 tumors (p<0.0001). There was no statistically significant difference in the recurrence score between the HER2-0 and the HER2-low subgroups.

Conclusion: Oncotype-DX single-gene scores for HER2 are a potential surrogate marker for assessing the precise HER2 status, with better reproducibility and less interobserver variance compared to immunohistochemistry. The use of rt-PCR emerges as an alternative method of assessment of the HER2-low subgroup.

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