Open AccessMedicine

María Luque-Cabal, P. García-Teijido, Y. Fernández-Pérez, Luisa Sánchez-Lorenzo, Isabel Palacio-Vázquez

2016.1.1Clinical Medicine Insights-Oncology

DOI: 10.4137/cmo.s34537

tlooto Summary

The introduction of trastuzumab therapy markedly improved the poor prognosis associated with HER2-amplified breast cancers and the identification of resistance mechanisms and the incorporation of new drugs that achieve a better blockade of HER family receptors signaling have resulted in improved outcomes.

Abstract

The introduction of trastuzumab therapy markedly improved the poor prognosis associated with HER2-amplified breast cancers. Despite this, the presence of primary and acquired resistance to trastuzumab treatment remains a significant common challenge. The identification of resistance mechanisms and the incorporation of new drugs that achieve a better blockade of HER family receptors signaling have resulted in improved outcomes. The phosphatidylinositol 3'-kinase/protein kinase B/mammalian target of rapamycin pathway, cross-talk with estrogen receptors, immune response, cell cycle control mechanisms, and other tyrosine kinase receptors such as insulin-like growth factor I receptor are potential pathways involved in trastuzumab resistance. Different therapeutic interventions targeting these pathways are currently under evaluation.

Citation format

LUQUE-CABAL, María, et al. Mechanisms behind the resistance to trastuzumab in her2-amplified breast cancer and strategies to overcome it. Clinical Medicine Insights-Oncology, 2016, 10: 21–30.