Review of the status of neoadjuvant therapy in HER2-positive breast cancer

被引:18
作者
Dowling, Gavin P. [1 ,2 ,3 ]
Keelan, Stephen [2 ,3 ]
Toomey, Sinead [1 ]
Daly, Gordon R. [2 ,3 ]
Hennessy, Bryan T. [1 ]
Hill, Arnold D. K. [2 ,3 ]
机构
[1] Royal Coll Surgeons Ireland, Dept Mol Med, Med Oncol Lab, Dublin, Ireland
[2] Royal Coll Surgeons Ireland, Dept Surg, Dublin, Ireland
[3] Beaumont Hosp, Dept Surg, Dublin, Ireland
关键词
neoadjuvant therapy; breast cancer; HER2 (human epidermal growth factor 2); targeted therapy; biomarker; antibody-drug-conjugates; PATHOLOGICAL COMPLETE RESPONSE; CHEMOTHERAPY PLUS TRASTUZUMAB; LONG-TERM OUTCOMES; ADJUVANT TRASTUZUMAB; OPEN-LABEL; SURVIVAL OUTCOMES; FINAL ANALYSIS; FOLLOW-UP; LAPATINIB; PERTUZUMAB;
D O I
10.3389/fonc.2023.1066007
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
PurposeThe development of human epidermal growth factor receptor 2 (HER2)-directed therapies has revolutionized the treatment of HER2-positive breast cancer. The aim of this article is to review the continually evolving treatment strategies in the neoadjuvant setting of HER2-positive breast cancer, as well as the current challenges and future perspectives. MethodsSearches were undertaken on PubMed and Clinicaltrials.gov for relevant publications and trials. FindingsThe current standard of care in high-risk HER2-positive breast cancer is to combine chemotherapy with dual anti-HER2 therapy, for a synergistic anti-tumor effect. We discuss the pivotal trials which led to the adoption of this approach, as well as the benefit of these neoadjuvant strategies for guiding appropriate adjuvant therapy. De-escalation strategies are currently being investigated to avoid over treatment, and aim to safely reduce chemotherapy, while optimizing HER2-targeted therapies. The development and validation of a reliable biomarker is essential to enable these de-escalation strategies and personalization of treatment. In addition, promising novel therapies are currently being explored to further improve outcomes in HER2-positive breast cancer.
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收藏
页数:10
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