HER2-low expression in patients with advanced or metastatic solid tumors

医学 免疫组织化学 乳腺癌 一致性 转移性乳腺癌 癌症 病理 HER2/东北 曲妥珠单抗 基因复制 肿瘤科 原发性肿瘤 内科学 转移 生物 基因 生物化学
作者
Burak Uzunparmak,Cara Haymaker,Gabriela Raso,Serena Masciari,Lei Wang,Heather Lin,Ayşegül Görür,Brian J. Kirby,Antonino Cimò,Amber M. Kennon,Qingqing Ding,Gabriele E Urschel,Ying Yuan,Guoying Feng,Yasmeen Q. Rizvi,Ahmad Fawzi Hussain,Chenjing Zhu,Phillip Kim,Giovanni Abbadessa,Vivek Subbiah
出处
期刊:Annals of Oncology [Elsevier BV]
卷期号:34 (11): 1035-1046 被引量:68
标识
DOI:10.1016/j.annonc.2023.08.005
摘要

Human epidermal growth factor receptor 2 (HER2)-low is a newly defined category with HER2 1+ or 2+ expression by immunohistochemistry (IHC) and lack of HER2 gene amplification measured by in situ hybridization (ISH). Much remains unknown about the HER2-low status across tumor types and changes in HER2 status between primary and metastatic samples.HER2 expression by IHC was evaluated in 4701 patients with solid tumors. We have evaluated the HER2 expression by IHC and amplification by ISH in paired breast and gastric/gastroesophageal (GEJ) primary and metastatic samples. HER2 expression was correlated with ERBB2 genomic alterations evaluated by next-generation sequencing (NGS) in non-breast, non-gastric/GEJ samples.HER2 expression (HER2 IHC 1-3+) was found in half (49.8%) of the cancers, with HER2-low (1 or 2+) found in many tumor types: 47.1% in breast, 34.6% in gastric/GEJ, 50.0% in salivary gland, 46.9% in lung, 46.5% in endometrial, 46% in urothelial, and 45.5% of gallbladder cancers. The concordance evaluation of HER2 expression between primary and metastatic breast cancer samples showed that HER2 3+ remained unchanged in 87.1% with a strong agreement between primary and metastatic samples, with a weighted kappa (Κ) of 0.85 (95% confidence interval 0.79-0.91). ERBB2 alterations were identified in 117 (7.5%) patients with non-breast, non-gastric/GEJ solid tumors who had NGS testing. Of 1436 patients without ERBB2 alterations, 512 (35.7%) showed any level HER2 expression by IHC.Our results show that HER2-low expression is frequently found across tumor types. These findings suggest that many patients with HER2-low solid tumors might benefit from HER2-targeted therapies.
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