Human epidermal receptor 2-amplified salivary duct carcinoma: Regression with dual human epidermal receptor 2 inhibition and anti-vascular endothelial growth factor combination treatment

被引:42
作者
Falchook, Gerald S. [1 ]
Lippman, Scott M. [2 ]
Bastida, Christel C. [1 ]
Kurzrock, Razelle [2 ]
机构
[1] Univ Texas MD Anderson Canc Ctr, Dept Invest Canc Therapeut, Phase Clin Trials Program 1, Houston, TX 77030 USA
[2] Univ Calif San Diego, Moores Canc Ctr, La Jolla, CA 92093 USA
来源
HEAD AND NECK-JOURNAL FOR THE SCIENCES AND SPECIALTIES OF THE HEAD AND NECK | 2014年 / 36卷 / 03期
基金
美国国家卫生研究院;
关键词
METASTATIC BREAST-CANCER; NERVOUS-SYSTEM PROGRESSION; CELL LUNG-CANCER; PHASE-II; LAPATINIB GW572016; GLAND TUMOR; TRASTUZUMAB; OVEREXPRESSION; C-ERBB-2; RADIOTHERAPY;
D O I
10.1002/hed.23429
中图分类号
R76 [耳鼻咽喉科学];
学科分类号
100213 ;
摘要
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.
引用
收藏
页码:E25 / E27
页数:3
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