This is a prospective clinical study aiming to tests the safety and efficacy of lenvatinib in combination with gefitinib in people with lenvatinib resistant hepatocellular carcinoma. This study will help find out if lenvatinib and gefitinib is a safe and useful combination for treating patients with lenvatinib resistant hepatocellular carcinoma.
Study Type
INTERVENTIONAL
Allocation
NA
Purpose
TREATMENT
Masking
NONE
Enrollment
30
First week: Gefitinib: 125mg/day, oral; Lenvatinib: 8mg/day (weight ≤ 60Kg) or 12mg/day (weight \> 60Kg), oral. One week later: Gefitinib: 250mg/day, oral; Lenvatinib: 8mg/day (weight ≤ 60Kg) or 12mg/day (weight \> 60Kg), oral.
Renji Hospital, School of Medicine, Shanghai Jiaotong University
Shanghai, Shanghai Municipality, China
Progression free survival
The estimation of time from start of combination therapy to progression of disease
Time frame: 6 months after the last subject is enrolled
Overall survival
The time between initial combination therapy and the patient's death of any cause or most recent follow-up.
Time frame: 6 months after the last subject is enrolled
Safety endpoint
Statistically describe the proportion of adverse events after treatment for each patient
Time frame: 6 months after the last subject is enrolled
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