HER2+ early breast cancer: from escalation via targeted and postneoadjuvant treatment to de-escalation

IF 4.6 Q2 MATERIALS SCIENCE, BIOMATERIALS ACS Applied Bio Materials Pub Date : 2023-10-25 DOI:10.1159/000534670
Monika Graeser, Oleg Gluz
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Abstract

Background: Human epidermal growth factor receptor 2 positive (HER2+, also referred to as ERBB2+) breast cancer is a subtype historically associated with a particularly poor prognosis. Research into biological and molecular pathomechanisms of breast cancer has resulted in the development and adoption of several therapies targeting HER2. In parallel, various escalation/de-escalation strategies have been examined to further optimize patient outcomes and care. Summary: In this review, we highlighted the landmark trials in the evolution of treatment and management of HER2+ early breast cancer. Key Messages: Continuous research over the last two decades has gradually prolonged survival in patients with early HER2+ early breast cancer. Incorporation of post-neoadjuvant setting into clinical practice improved long-term outcomes in high-risk patients with residual disease after neoadjuvant therapy. In parallel, use of modern anti-HER2 agents may potentially allow omission of chemotherapy without compromising the survival in a significant number of selected patients. Current research focused on exploring the molecular heterogeneity of HER2+ breast cancer resulted in identification of new prognostic and predictive biomarkers which could pave the way towards the development of truly personalized therapy.
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HER2+早期乳腺癌:通过靶向和新辅助治疗从升级到降级
背景:人表皮生长因子受体2阳性(HER2+,也称为ERBB2+)乳腺癌是一种历史上预后特别差的亚型。对乳腺癌生物学和分子病理机制的研究导致了几种靶向HER2的治疗方法的开发和采用。同时,还研究了各种升级/降级策略,以进一步优化患者的预后和护理。摘要:在这篇综述中,我们重点介绍了HER2+早期乳腺癌治疗和管理进展中具有里程碑意义的试验。关键信息:过去二十年的持续研究逐渐延长了早期HER2+早期乳腺癌患者的生存期。将后新辅助治疗纳入临床实践可改善新辅助治疗后遗留疾病的高危患者的长期预后。与此同时,使用现代抗her2药物可能会在不影响大量选定患者生存的情况下潜在地省略化疗。目前的研究重点是探索HER2+乳腺癌的分子异质性,从而确定新的预后和预测性生物标志物,这可能为真正个性化治疗的发展铺平道路。
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来源期刊
ACS Applied Bio Materials
ACS Applied Bio Materials Chemistry-Chemistry (all)
CiteScore
9.40
自引率
2.10%
发文量
464
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