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Human epidermal receptor 2–amplified salivary duct carcinoma: Regression with dual human epidermal receptor 2 inhibition and anti–vascular endothelial growth factor combination treatment
Author(s) -
Falchook Gerald S.,
Lippman Scott M.,
Bastida Christel C.,
Kurzrock Razelle
Publication year - 2014
Publication title -
head and neck
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.012
H-Index - 127
eISSN - 1097-0347
pISSN - 1043-3074
DOI - 10.1002/hed.23429
Subject(s) - lapatinib , medicine , trastuzumab , salivary duct carcinoma , bevacizumab , mucositis , oncology , salivary gland , salivary gland cancer , carcinoma , chemotherapy , cancer , cancer research , breast cancer
Background Salivary ductal carcinoma is a rare cancer with poor prognosis and limited treatment options. Human epidermal receptor 2 (HER2)‐directed treatment has been attempted in HER2‐amplified or overexpressed salivary gland malignancies with limited success. Methods We report resolution of measurable disease and minimal residual disease in a patient with salivary duct cancer treated with trastuzumab, lapatinib, and bevacizumab, with treatment ongoing for more than 2 years. Results This treatment has been tolerated well except for grade 2 diarrhea and mucositis, which required a dose reduction of lapatinib to 1000 mg daily. The response observed was achieved in spite of receiving extensive prior therapy, including trastuzumab and/or chemotherapy for 20 months on which his tumors progressed. Conclusion The combination of trastuzumab, lapatinib, and bevacizumab may warrant investigation as a non‐cytotoxic alternative for treatment of HER2‐amplified or overexpressed salivary duct carcinoma and other HER2‐amplified or overexpressed salivary gland tumors, particularly those not responsive to trastuzumab monotherapy. © 2013 Wiley Periodicals, Inc. Head Neck 36 : E25–E27, 2014