| Literature DB >> 33862249 |
Daniele Galanti1, Alessandro Inno2, Maria La Vecchia3, Nicolò Borsellino1, Lorena Incorvaia4, Antonio Russo5, Stefania Gori1.
Abstract
Brain metastases (BMs) are frequently associated with HER2+ breast cancer (BC). Their management is based on a multi-modal strategy including both local treatment and systemic therapy. Despite therapeutic advance, BMs still have an adverse impact on survival and quality of life and the development of effective systemic therapy to prevent and treat BMs from HER2 + BC represents an unmet clinical need. Trastuzumab-based therapy has long been the mainstay of systemic therapy and over the last two decades other HER2-targeted agents including lapatinib, pertuzumab and trastuzumab emtansine, have been introduced in the clinical practice. More recently, novel agents such as neratinib, tucatinib and trastuzumab deruxtecan have been developed, with interesting activity against BMs. Further research is needed to better elucidate the best sequence of these agents and their combination with local treatment.Entities:
Keywords: Brain metastases; HER2-positive breast cancer; Lapatinib; Neratinib; Trastuzumab; Trastuzumab deruxtecan; Trastuzumab-emtansine; Tucatinib
Year: 2021 PMID: 33862249 DOI: 10.1016/j.critrevonc.2021.103329
Source DB: PubMed Journal: Crit Rev Oncol Hematol ISSN: 1040-8428 Impact factor: 6.312