CELL INTELLIGENCE · 肿瘤细胞治疗研究
肿瘤细胞治疗研究
英文原题:Focusing on the Advances and Challenges of HER2-Targeted Therapy: Cutting-Edge Breakthroughs in Neoadjuvant Treatment for HER2-Positive Breast Cancer.
Focusing on the Advances and Challenges of HER2-Targeted Therapy: Cutting-Edge Breakthroughs in Neoadjuvant Treatment for HER2-Positive Breast Cancer.
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HER2阳性乳腺癌以人表皮生长因子受体2(HER2)过表达为特征,约占所有乳腺癌的15-20%,与肿瘤侵袭性行为和不良预后相关。HER2靶向治疗的进展,如单克隆抗体(曲妥珠单抗、帕妥珠单抗)、酪氨酸激酶抑制剂(TKIs)和抗体药物偶联物(ADCs),已显著改善了该亚型的治疗结局。新辅助治疗,即在手术前给药,通过提高病理完全缓解(pCR)率和生存结局,已成为管理HER2阳性乳腺癌的基石。本综述全面分析了HER2靶向新辅助治疗的最新进展,重点阐述了其作用机制、临床疗效以及与化疗联合时的协同效应。讨论了关键挑战,如治疗相关毒性,以及基于生物标志物如TIL(肿瘤浸润淋巴细胞)(TILs)和HER2富集亚型的个性化治疗策略的潜力。未来方向强调优化治疗方案以提高疗效同时最小化不良反应,新型药物如曲妥珠单抗德鲁替康(T-DXd)显示出拓展治疗格局的前景。
HER2-positive breast cancer, characterized by overexpression of the human epidermal growth factor receptor 2 (HER2), accounts for approximately 15-20% of all breast cancers and is associated with aggressive tumor behavior and poor prognosis. Advances in HER2-targeted therapies, such as monoclonal antibodies (trastuzumab, pertuzumab), tyrosine kinase inhibitors (TKIs), and antibody-drug conjugates (ADCs), have significantly improved treatment outcomes in this subtype. Neoadjuvant therapy, administered before surgery, has become a cornerstone in managing HER2-positive breast cancer by improving pathological complete response (pCR) rates and survival outcomes.
This review provides a comprehensive analysis of recent advancements in HER2-targeted neoadjuvant therapies, highlighting the mechanisms of action, clinical efficacy, and synergistic effects when combined with chemotherapy. Key challenges, such as treatment-related toxicities, and the potential for personalized treatment strategies based on biomarkers like tumor-infiltrating lymphocytes (TILs) and HER2-enriched subtypes, are discussed.
Future directions emphasize optimizing treatment regimens to enhance efficacy while minimizing adverse effects, with novel agents such as trastuzumab deruxtecan (T-DXd) showing promise for expanding the therapeutic landscape.
在 PubMed 查看 → 出版商原文(DOI) 全文 PDF(PMC)· 可下载 治疗专题与资料阅读指南 资料来源与翻译说明 报告译文或资料问题 →
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