TY - JOUR
T1 - Personalized drug combinations to overcome trastuzumab resistance in HER2-positive breast cancer
AU - Vu, Thuy
AU - Sliwkowski, Mark X.
AU - Claret, Francois X.
N1 - Funding Information:
This project was sponsored by grants from the NIH ( R01-CA90853 ) and Cancer Prevention Research Institute of Texas ( RP120451 ) (to F.X. Claret); by the Vietnam Education Foundation (to T. Vu); and by MD Anderson's Cancer Center Support Grant ( CA016672 ). We thank Ann M. Sutton for editing the manuscript.
PY - 2014/12
Y1 - 2014/12
N2 - 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.
AB - 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.
KW - Combination approaches
KW - HER2-positive breast cancer
KW - Targeted therapy
KW - Trastuzumab resistance
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U2 - 10.1016/j.bbcan.2014.07.007
DO - 10.1016/j.bbcan.2014.07.007
M3 - Review article
C2 - 25065528
AN - SCOPUS:84906707906
SN - 0304-419X
VL - 1846
SP - 353
EP - 365
JO - Biochimica et Biophysica Acta - Reviews on Cancer
JF - Biochimica et Biophysica Acta - Reviews on Cancer
IS - 2
ER -