Prediction of response to anti-HER2 therapy using a multigene assay.

IF 7.1 1区 医学 Q1 PATHOLOGY Modern Pathology Pub Date : 2025-01-16 DOI:10.1016/j.modpat.2025.100713
Nehal Atallah, Shorouk Makhlouf, X M Li, Y Zhang, Nigel P Mongan, Emad Rakha
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Abstract

HER2-positive breast cancer (BC), which constitutes 13-15% of cases, shows variable response to anti-HER2 therapies. HER2-positivity, defined as protein overexpression (immunohistochemistry (IHC) score 3+) or equivocal expression (IHC 2+) with evidence of HER2 gene amplification, determines the eligibility to anti-HER2 therapy. MammaTyper® assay (Cerca Biotech GmbH) is a RT-qPCR BC subtyping platform based on the mRNA expression of ERBB2, ESR1, PGR, and MKI67. This study aims to evaluate the accuracy of the MammaTyper® assay in predicting the response of HER2-positive patients to therapy. A well-characterized HER2-positive BC cohort of 287 cases diagnosed at Nottingham University hospitals between 2006 and 2018 was included. The cohort was divided into 2 groups: a trastuzumab-treated group (n=159) and a chemotherapy-only treated group (n=128). Tumor clinicopathologic characteristics were matched between the two groups. Cases with discordant HER2 status were validated through staining of surgical excision specimens. ERBB2 mRNA identified 251/287 (87.5%) cases as HER2-positive, 10.8% (31/287) as HER2 low and 1.7% (5/287) as HER2-negative. According to MammaTyper® assay, ERBB2-positive patients treated with anti-HER2 therapy had significantly prolonged 5-year disease (DFS) and distant metastasis (DMFS) free survival (HR=0.56, p=0.003 and HR=0.62, p=0.023, respectively). MammaTyper®-defined HER2-Enriched subtype showed better response to anti-HER2 therapy compared to IHC-defined subtypes, with significant differences in both 5-year DFS and BCSS (p=0.01 and <0.001, respectively). ERBB2-negative patients did not show survival difference between the group of patients who were treated with trastuzumab and those who were treated with chemotherapy only (p>0.05). Validation analysis revealed that 11/36 ERBB2-negative cases were IHC 2+/ISH positive with very low level of gene amplification and 25 cases were false classified as HER2 positive using current protocols. Combining MammaTyper® assay with IHC to assess HER2 status improves the identification of HER2-positive BC patients who would benefit from anti-HER2 therapy.

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使用多基因分析预测抗her2治疗的反应。
her2阳性乳腺癌(BC)占病例的13-15%,对抗her2治疗表现出不同的反应。HER2阳性,定义为蛋白质过表达(免疫组织化学(IHC)评分3+)或模糊表达(IHC 2+),有HER2基因扩增的证据,决定了抗HER2治疗的资格。MammaTyper®检测(Cerca Biotech GmbH)是基于ERBB2、ESR1、PGR和MKI67 mRNA表达的RT-qPCR BC亚型分型平台。本研究旨在评估MammaTyper®检测在预测her2阳性患者对治疗反应方面的准确性。纳入了2006年至2018年期间在诺丁汉大学医院诊断的287例典型的her2阳性BC队列。该队列分为2组:曲妥珠单抗治疗组(n=159)和单纯化疗组(n=128)。两组肿瘤临床病理特征吻合。HER2状态不一致的病例通过手术切除标本染色进行验证。ERBB2 mRNA鉴定251/287例(87.5%)为HER2阳性,10.8%(31/287)为HER2低,1.7%(5/287)为HER2阴性。根据MammaTyper®检测,接受抗her2治疗的erbb2阳性患者的5年疾病(DFS)和无远处转移(DMFS)生存期显著延长(HR=0.56, p=0.003和HR=0.62, p=0.023)。与ihc定义的亚型相比,MammaTyper®定义的her2富集亚型对抗her2治疗的反应更好,在5年DFS和BCSS方面存在显著差异(p=0.01和0.05)。验证分析显示,11/36例erbb2阴性病例为IHC 2+/ISH阳性,基因扩增水平极低,25例根据现行方案被错误地分类为HER2阳性。结合MammaTyper®检测和免疫组化(IHC)来评估HER2状态,可以提高HER2阳性BC患者的识别,这些患者将从抗HER2治疗中获益。
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来源期刊
Modern Pathology
Modern Pathology 医学-病理学
CiteScore
14.30
自引率
2.70%
发文量
174
审稿时长
18 days
期刊介绍: Modern Pathology, an international journal under the ownership of The United States & Canadian Academy of Pathology (USCAP), serves as an authoritative platform for publishing top-tier clinical and translational research studies in pathology. Original manuscripts are the primary focus of Modern Pathology, complemented by impactful editorials, reviews, and practice guidelines covering all facets of precision diagnostics in human pathology. The journal's scope includes advancements in molecular diagnostics and genomic classifications of diseases, breakthroughs in immune-oncology, computational science, applied bioinformatics, and digital pathology.
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