| Literature DB >> 33245671 |
Chiara Molinelli1, Francesca Parisi2, Maria Grazia Razeti2, Luca Arecco2, Maurizio Cosso3, Piero Fregatti4,5, Lucia Del Mastro1,6, Francesca Poggio1, Matteo Lambertini2,6.
Abstract
Introduction: The prognosis of patients with HER2-positive early breast cancer has radically improved after the introduction of (neo)adjuvant anti-HER2 targeted therapy. Trastuzumab emtansine (T-DM1) is an antibody-drug conjugate combining the anticancer properties of the anti-HER2 agent trastuzumab and the antineoplastic cytotoxic drug DM1. After demonstrating to be an effective and safe treatment for patients with HER2-positive advanced breast cancer, the development of T-DM1 has moved to the early setting.Areas covered: The aim of this review is to explore the current role of T-DM1 in the treatment landscape of HER2-positive early breast cancer, focusing specifically on the efficacy and safety data available in the adjuvant setting.Expert opinion: T-DM1 is an effective and safe treatment option in the adjuvant setting for patients with HER2-positive breast cancer without pathologic complete response after standard neoadjuvant chemotherapy plus anti-HER2 targeted therapy. With the availability of more effective anti-HER2 targeted agents, including T-DM1, there is an urgent need for more chemotherapy de-escalation research efforts in the early setting.Entities:
Keywords: Antibody-drug conjugate; HER2-positive; breast cancer; t-DM1; trastuzumab emtansine
Year: 2020 PMID: 33245671 DOI: 10.1080/14737140.2021.1857243
Source DB: PubMed Journal: Expert Rev Anticancer Ther ISSN: 1473-7140 Impact factor: 4.512