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Study identifier: NCT06788353 Synced from ClinicalTrials.gov · July 29, 2026
● Recruiting

Prospective Collection of Therapeutic Efficacy and Safety Data in Patients with Unresectable Hepatocellular Carcinoma

Condition: Transarterial Chemoembolization · Systemic Therapy · Unresectable Hepatocellular Carcinoma  ·  Sponsor: Sun Yat-sen University

PhaseN/A
Planned participants500
Who can joinAll sexes, 18 Years to 75 Years
Healthy volunteersNo

About this study

The malignant degree of middle and advanced liver cancer is very high, and the survival prognosis of patients is very poor. TACE is currently the standard treatment for unresectable liver cancer recommended by several international authoritative guidelines. However, TACE can only extend survival from 8 months to 13 months, and the prognosis for patients with unresectable liver cancer is still not optimistic. In recent years, some studies have suggested that the combination of TACE and systemic therapy can prolong OS and PFS, but a number of prospective studies have found that the combination of TACE and targeted therapy can not improve the prognosis of unresectable liver cancer. However, TACE as a non-radical treatment is difficult to achieve complete tumor necrosis, so it is still unknown which treatment combination can best improve the prognosis. This trial is an observational clinical trial to explore the efficacy and safety of TACE combined targeting/immunotherapy for unresectable hepatocellular carcinoma. Clinical data of patients with unresectable liver cancer treated in our hospital from March 2023 to March 2025 are intended to be collected to evaluate the efficacy and safety of TACE combined with different systems for unresectable liver cancer.

This description comes directly from the study's public registry record.

Talk to the study team

Zhenwei Peg, Dr.  ·  86+18620565282  ·  pzhenw@mail.sysu.edu.cn

Always discuss trial participation with your own doctor first.

Locations (1)

The First Affiiated Hospital of Sun Yat-sen UniversityGuangzhou, Guangdong, ChinaRecruiting

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Source record: clinicaltrials.gov/study/NCT06788353