Stage IV Squamous Cell Carcinoma of the Hypopharynx Clinical Trial
Official title:
A Phase II Study Of GW572016 In Squamous Cell Carcinoma Of The Head And Neck (SCCHN)
Lapatinib may stop the growth of tumor cells by blocking some of the enzymes needed for their growth. This phase II trial is studying how well lapatinib works in treating patients with recurrent and/or metastatic head and neck cancer.
PRIMARY OBJECTIVES:
I. Determine the overall response rate in patients with recurrent and/or metastatic squamous
cell carcinoma of the head and neck treated with lapatinib.
II. Determine the progression-free survival, time to progression, and overall survival of
patients treated with this drug.
III. Determine the toxicity of this drug in these patients.
OUTLINE: This is a multicenter study. Patients are assigned to 1 of 2 cohorts according to
prior epidermal growth factor receptor-targeted therapy (yes vs no).
Patients receive oral lapatinib once daily on days 1-28. Courses repeat every 28 days in the
absence of disease progression or unacceptable toxicity.
Patients are followed every 2 months.
PROJECTED ACCRUAL: A total of 40-88 patients (21-50 epidermal growth factor receptor [EGFR]
inhibitor-naive patients [cohort A] and 19-38 EGFR inhibitor-pre-treated patients [cohort
B]) will be accrued for this study within 4-12.6 months.
;
Endpoint Classification: Efficacy Study, Intervention Model: Single Group Assignment, Masking: Open Label, Primary Purpose: Treatment
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