Single Arm, Phase II Study of Cisplatin, Docetaxel, and Erlotinib in Patients with Recurrent and/or Metastatic Head and Neck Squamous Cell Carcinomas

被引:17
作者
William, William N., Jr. [1 ]
Tsao, Anne S. [1 ]
Feng, Lei [1 ]
Ginsberg, Lawrence E. [1 ]
Lee, J. Jack [1 ]
Kies, Merrill S. [1 ]
Glisson, Bonnie S. [1 ]
Kim, Edward S. [2 ]
机构
[1] Univ Texas MD Anderson Canc Ctr, 1515 Holcombe Blvd,Unit 432, Houston, TX 77030 USA
[2] Levine Canc Inst, Charlotte, NC USA
关键词
OPEN-LABEL; TRIAL; CHEMOTHERAPY; CANCER; GEFITINIB; CETUXIMAB; METHOTREXATE; COMBINATION; EXTREME;
D O I
10.1634/theoncologist.2017-0661
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Background. The epidermal growth factor receptor (EGFR) plays a key role in the carcinogenesis of head and neck squamous cell carcinomas (HNSCC). We conducted this clinical study to test the hypothesis that the addition of erlotinib to first-line cisplatin and docetaxel for patients with recurrent and/ormetastatic HNSCC would yield a response rate of at least 50%, representing an improvement from historical controls. Methods. Patients with recurrent and/or metastatic HNSCC, with at least one measurable lesion, no prior chemotherapy for recurrent and/or metastatic disease, prior combined modality therapy completed >6 months before enrollment, and performance status <= 2 were treated with cisplatin, docetaxel, and erlotinib for up to six cycles, followed by maintenance erlotinib until disease progression. The primary endpoint was response rate. Results. Fifty patients were enrolled (42 male, 12 never smokers, 19 with oropharynx cancer). The median number of cycles was five; 31 patients initiated maintenance erlotinib; 14 patients required erlotinib dose reductions. The objective response rate was 62%, and the median progression-free and overall survival were 6.1 and 11.0 months, respectively. Toxicity profiles were consistent with the known side effects of the study drugs. Conclusion. The study met its primary endpoint and improved response rates compared with historical controls. The findings support further evaluation of the regimen for recurrent and/or metastatic HNSCCs.
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页码:526 / +
页数:7
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