Literature DB >> 25065528

Personalized drug combinations to overcome trastuzumab resistance in HER2-positive breast cancer.

Thuy Vu1, Mark X Sliwkowski2, Francois X Claret3.   

Abstract

HER2-positive (HER2+) breast cancer accounts for 18%-20% of all breast cancer cases and has the second poorest prognosis among breast cancer subtypes. Trastuzumab, the first Food and Drug Administration-approved targeted therapy for breast cancer, established the era of personalized treatment for HER2+ metastatic disease. It is well tolerated and improves overall survival and time-to-disease progression; with chemotherapy, it is part of the standard of care for patients with HER2+ metastatic disease. However, many patients do not benefit from it because of resistance. Substantial research has been performed to understand the mechanism of trastuzumab resistance and develop combination strategies to overcome the resistance. In this review, we provide insight into the current pipeline of drugs used in combination with trastuzumab and the degree to which these combinations have been evaluated, especially in patients who have experienced disease progression on trastuzumab. We conclude with a discussion of the current challenges and future therapeutic approaches to trastuzumab-based combination therapy.
Copyright © 2014 Elsevier B.V. All rights reserved.

Entities:  

Keywords:  Combination approaches; HER2-positive breast cancer; Targeted therapy; Trastuzumab resistance

Mesh:

Substances:

Year:  2014        PMID: 25065528      PMCID: PMC4261073          DOI: 10.1016/j.bbcan.2014.07.007

Source DB:  PubMed          Journal:  Biochim Biophys Acta        ISSN: 0006-3002


  123 in total

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Journal:  Oncogene       Date:  2009-10-26       Impact factor: 9.867

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7.  HER2+ Cancer Cell Dependence on PI3K vs. MAPK Signaling Axes Is Determined by Expression of EGFR, ERBB3 and CDKN1B.

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10.  Identification of novel pathways linking epithelial-to-mesenchymal transition with resistance to HER2-targeted therapy.

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