Molecular Targeting Unit, Department of Research, Fondazione IRCCS Istituto Nazionale dei Tumori, Milan, Italy.
Dis Markers. 2017;2017:7849108. doi: 10.1155/2017/7849108. Epub 2017 Dec 18.
HER2 is overexpressed in 20% of invasive breast cancers (BCs) and correlates with a more aggressive disease. Until the advent of targeted agents, HER2 was associated with worse outcomes. Rationally designed HER2-targeted agents have been developed and introduced into clinical practice for women with HER2-amplified BC, improving disease-free and overall survival for primary and metastatic tumors. Trastuzumab, a recombinant humanized anti-HER2 monoclonal antibody, combined with chemotherapy, remains the standard of care for patients with HER2-positive BCs. However, many patients do not respond to this agent, whereas newer drugs have proven to be efficacious in clinical trials. The identification of biomarkers that select sensitive tumors and patients who will benefit from these new agents would help the incorporation of these therapies, limiting the risk of side effects and overtreatment and improving the outcomes of all patients with early-stage HER2-positive BC. We review the mechanisms of action of HER2-targeting agents, focusing on the involvement of the immune system and related predictive biomarkers.
HER2 在 20%的浸润性乳腺癌(BC)中过表达,与更具侵袭性的疾病相关。在靶向药物出现之前,HER2 与更差的预后相关。为了治疗 HER2 扩增的 BC 患者,已经开发并引入了具有合理设计的 HER2 靶向药物,改善了原发性和转移性肿瘤的无病生存和总生存。曲妥珠单抗,一种重组人源化抗 HER2 单克隆抗体,与化疗联合使用,仍然是 HER2 阳性 BC 患者的标准治疗方法。然而,许多患者对此药物没有反应,而新型药物已在临床试验中证明有效。识别能够选择敏感肿瘤和从这些新药物中获益的患者的生物标志物,将有助于这些疗法的应用,限制副作用和过度治疗的风险,并改善所有早期 HER2 阳性 BC 患者的结局。我们回顾了 HER2 靶向药物的作用机制,重点关注免疫系统的参与和相关的预测性生物标志物。