This phase I/II clinical trial aims to determine the efficacy and safety of TATE compared to TACE in patients with intermediate-stage HCC. The results will provide valuable insights into the potential benefits of TATE as a novel treatment option for HCC.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
SINGLE
Enrollment
300
Intra-arterial injection into the tumor feeding artery
Lipiodol and Gelfoam used to embolize tumor vessels and induce tumor hypoxia
TACE with epirubicin
Zhongda Hospital, Affiliated to Southeast University
Nanjing, Jiangsu, China
RECRUITINGLishui Central Hospital
Lishui, Zhejiang, China
RECRUITINGProgression-free survival (PFS)
Progression-free survival (PFS) assessed by the Independent Radiology Committee (IRC) using mRECIST criteria.
Time frame: 36 months
Complete Response (CR) rate
Complete response rate (CR) assessed by IRC using mRECIST criteria
Time frame: 36 months
objective response rate (ORR)
Time frame: 36 months
duration of complete response (DOCR)
Time frame: 36 months
overall survival (OS)
Time frame: 36 months
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