z-logo
open-access-imgOpen Access
Anti-HER2 Therapy Beyond Second-Line for HER2- Positive Metastatic Breast Cancer: A Short Review and Recommendations for Several Clinical Scenarios from a Spanish Expert Panel
Author(s) -
Noelia Martínez-Jáñez,
Ignacio Fernández Chacón,
Ana De Juan,
Luis de la Cruz-Merino,
Sonia Del Barco,
I. Fernández,
Paula García-Teijido,
Amalia Gómez-Bernal,
Arrate Plazaola,
José Ponce,
Sònia Servitja,
Pilar Zamora
Publication year - 2016
Publication title -
breast care
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.767
H-Index - 30
eISSN - 1661-3805
pISSN - 1661-3791
DOI - 10.1159/000443601
Subject(s) - medicine , metastatic breast cancer , breast cancer , oncology , medical physics , panel discussion , cancer , intensive care medicine , advertising , business
Background: The aim of this project was to provide an expert opinion regarding anti-human epidermal growth factor receptor 2 (HER2) therapy beyond second-line treatment of metastatic breast cancer (mBC). Methods: A group of experts discussed specific issues concerning anti-HER2 therapy in late-line settings in mBC. Results: Trastuzumab emtansine (T-DM1) or dual HER2 blockade appeared to be good options for HER2-positive mBC after ≥ 2 HER2-targeted therapies. Once an objective response has been achieved with anti-HER2-containing therapy, the anti-HER2 agent can be continued until progression of the disease, unacceptable toxicity or patient decision. mBC treated with ≥ 3 consecutive lines of anti-HER therapy, ≥ 1 being a dual HER2 blockade and with early progression of disease during a fourth or later-line treatment, are clinically resistant to anti-HER therapy. For progression of metastasis in the brain after anti-HER2 therapy, lapatinib and chemotherapy appear to be a good alternative after best local treatment. Conclusions: Further clinical trials are needed to provide valuable knowledge about the best treatment options in the later settings of mBC.

The content you want is available to Zendy users.

Already have an account? Click here to sign in.
Having issues? You can contact us here