提高HER2低水平乳腺癌中HER2检测的可重复性。

IF 4.6 Q1 ONCOLOGY
Elham Sajjadi, Konstantinos Venetis, Mariia Ivanova, Nicola Fusco
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引用次数: 11

摘要

HER2是乳腺癌的主要生物标志物,通过免疫组织化学(IHC)使用三层评分系统和反射原位杂交(ISH)对IHC评分为2+进行评估。新型HER2定向抗体-药物偶联物在HER2低表达水平(即IHC评分为1+或ish阴性IHC评分为2+)的乳腺癌中显示出显著的抗肿瘤活性。根据HER2阳性连续体,抗HER2治疗的原发性和获得性耐药仍然是乳腺癌治疗中的一个挑战。因此,精确区分her2 - 0、her2 -低和her2 -阳性乳腺癌的能力不再仅仅是一个学术练习。针对这一新的临床需求,HER2检测标准、指南和质量控制正在重新获得动力。因此,应仔细考虑所有可能影响该试验敏感性和可重复性的分析前和分析变量,以解决所有可能的问题,并为乳腺癌患者打开所有可能的治疗机会。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Improving HER2 testing reproducibility in HER2-low breast cancer.

HER2 is a pillar biomarker in breast cancer, and it is assessed by immunohistochemistry (IHC) using a three-tier scoring system and reflex in situ hybridization (ISH) for IHC score 2+. Novel HER2-directed antibody-drug conjugates have demonstrated significant antitumor activity in breast cancers with low levels of HER2 expression, i.e. IHC score 1+ or ISH-negative IHC score 2+. Both primary and acquired resistance to anti-HER2 therapies remains a challenge in the treatment of breast cancers according to the HER2 positivity continuum. Thus, the ability to precisely discriminate among HER2-zero, HER2-low, and HER2-positive breast cancers is no longer a mere academic exercise. HER2 testing criteria, guidelines, and quality controls are re-gaining momentum for this new clinical need. Therefore, all preanalytical and analytical variables that might trouble the sensitivity and reproducibility of this test should be carefully considered to address all possible issues and open all possible therapeutic opportunities for breast cancer patients.

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