This is a phase 2 study to evaluate the efficacy of single-agent icotinib in patients with advanced nasopharyngeal carcinoma.
This phase 2 study is aimed to evaluate the efficacy of single-agent icotinib in patients with pretreated, advanced nasopharyngeal carcinoma. The primary endpoint is disease control rate (DCR).
Study Type
INTERVENTIONAL
Allocation
NA
Purpose
TREATMENT
Masking
NONE
Enrollment
66
Icotinib (125 mg tablet) is orally administered three times daily until disease progression or unaccepted toxicity.
Disease control rate(DCR)
Time frame: At least 8 weeks
Progression-free survival
Time frame: At least 8 weeks
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