evaluation of the efficacy of transarterial chemoinfusion (TAI) combine lenvatinib in advanced hepatocelllar carcinoma
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Enrollment
206
TAI combine lenvatinib
lenvatinib only
SUN YAT-SEN University Cancer Center
Guangzhou, Guangdong, China
RECRUITINGOS
overall survival
Time frame: From date of randomization until the date of death from any cause, assessed up to 60 months
PFS
progression-free survival
Time frame: From date of randomization until the date of progress from any cause, assessed up to 60 months
ORR
object response rate
Time frame: From date of randomization until the date of death from any cause, assessed up to 60 months
DCR
disease control rate
Time frame: From date of randomization until the date of death from any cause, assessed up to 60 months
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