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