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Management of patients with advanced-stage HER2-positive breast cancer: current evidence and future perspectives.
Marra, Antonio; Chandarlapaty, Sarat; Modi, Shanu.
Affiliation
  • Marra A; Division of New Drugs and Early Drug Development, European Institute of Oncology IRCCS, Milan, Italy.
  • Chandarlapaty S; Human Oncology and Pathogenesis Program (HOPP), Memorial Sloan Kettering Cancer Center, New York, NY, USA.
  • Modi S; Breast Medicine Service, Department of Medicine, Memorial Sloan Kettering Cancer Center, New York, NY, USA.
Nat Rev Clin Oncol ; 21(3): 185-202, 2024 Mar.
Article in En | MEDLINE | ID: mdl-38191924
ABSTRACT
Amplification and/or overexpression of ERBB2, the gene encoding HER2, can be found in 15-20% of invasive breast cancers and is associated with an aggressive phenotype and poor clinical outcomes. Relentless research efforts in molecular biology and drug development have led to the implementation of several HER2-targeted therapies, including monoclonal antibodies, tyrosine-kinase inhibitors and antibody-drug conjugates, constituting one of the best examples of bench-to-bedside translation in oncology. Each individual drug class has improved patient outcomes and, importantly, the combinatorial and sequential use of different HER2-targeted therapies has increased cure rates in the early stage disease setting and substantially prolonged survival for patients with advanced-stage disease. In this Review, we describe key steps in the development of the modern paradigm for the treatment of HER2-positive advanced-stage breast cancer, including selecting and sequencing new-generation HER2-targeted therapies, and summarize efficacy and safety outcomes from pivotal studies. We then outline the factors that are currently known to be related to resistance to HER2-targeted therapies, such as HER2 intratumoural heterogeneity, activation of alternative signalling pathways and immune escape mechanisms, as well as potential strategies that might be used in the future to overcome this resistance and further improve patient outcomes.
Subject(s)

Full text: 1 Database: MEDLINE Main subject: Breast Neoplasms / Antineoplastic Agents Limits: Female / Humans Language: En Year: 2024 Type: Article

Full text: 1 Database: MEDLINE Main subject: Breast Neoplasms / Antineoplastic Agents Limits: Female / Humans Language: En Year: 2024 Type: Article