The investigators will examine efficacy and toxicity of gefitinib in Korean patients with EGFR wild tumors diagnosed with direct sequence test.
Study Type
INTERVENTIONAL
Allocation
NA
Purpose
TREATMENT
Masking
NONE
Enrollment
92
Iressa 250mg per day until progression
Samsung Medical Center
Seoul, South Korea
NOT_YET_RECRUITINGSamsung Medical Center
Seoul, South Korea
RECRUITINGTo determine disease control rate at 8 weeks will be 35% or higher in the the study group
Time frame: 6 months after the enrollment of the last patients
The number of patients who live longer than 6 months after enrollment
Time frame: 6 months after the enrollment of the last patients
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