The change of paradigm in the treatment of HER2-positive breast cancer with the development of new generation antibody-drug conjugates

Other authors

Institut Català de la Salut

Medical Oncology Service, Breast Cancer Unit, Vall d’Hebron Institute of Oncology (VHIO), Barcelona, Spain

Vall d'Hebron Barcelona Hospital Campus

Publication date

2023-05-02T10:57:10Z

2023-05-02T10:57:10Z

2023-01-12



Abstract

Breast cancer; HER2-positive; New drugs


Càncer de mama; HER2-positiu; Nous medicaments


Cáncer de mama; HER2 positivo; Nuevos fármacos


HER2-positive breast cancer is an aggressive disease. As a result of the development of specific HER2-targeted therapies, such as trastuzumab, more than 20 years ago, the prognosis of these patients has improved. Metastatic HER2-positive breast cancer patients are achieving better survival rates upon treatment with anti-HER2 therapies than patients with HER2-negative disease. Double HER2 blockade with trastuzumab and pertuzumab combined with a taxane achieved an unprecedented survival of over 57 months in first-line patients. Trastuzumab emtansine, the first antibody-drug conjugate approved for patients in second-line treatment was a potent cytotoxic agent bound to trastuzumab and is currently a standard therapeutic strategy. Despite the progress in treatment development, most patients develop resistance and eventually relapse. Advances in the design of antibody-drug conjugates have led to the development of new generation drugs with enhanced properties, such as trastuzumab deruxtecan and trastuzumab duocarmazine, which are significantly changing the paradigm in the treatment of HER2-positive metastatic breast cancer.

Document Type

Article


Published version

Language

English

Publisher

OAE Publishing

Related items

Cancer Drug Resistance;6

http://dx.doi.org/10.20517/cdr.2022.52

Recommended citation

This citation was generated automatically.

Rights

Attribution 4.0 International

http://creativecommons.org/licenses/by/4.0/

This item appears in the following Collection(s)