The current random, double-blind, controlled, clinical trial was designed to evaluate the impact on therapeutic effect and tolerance of treatment for patients with hepatocelluclar carcinoma in transcatheter arterial chemoembolization (TACE) of dexamethasone application.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
QUADRUPLE
Enrollment
220
use dexamethasone 10mg (2ml) I.A. during TACE
use normal saline 2ml I.A. during TACE
Cancer Center of Sun Yat-Sen University
Guangzhou, Guangdong, China
RECRUITINGresponse rate (RR)
Time frame: 1 month after TACE
proportions of participants with severe adverse events according to CTCAE v4.03
Time frame: 1 month after TACE
overall survival (OS)
Time frame: From date of randomization until the date of death from any cause, assessed up to 60 months
progression-free survival (PFS)
Time frame: From date of randomization until the date of first documented progression or date of death from any cause, whichever came first, assessed up to 60 months
time to progression (TTP)
Time frame: From date of randomization until the date of first documented progression or date of death from any cause, whichever came first, assessed up to 60 months
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