Skip to content

TACE combined with immunotherapy plus targeted therapy and immunotherapy plus targeted therapy alone in advanced liver cancer: a comparative effectiveness and efficacy prediction study

TACE combined with immunotherapy plus targeted therapy and immunotherapy plus targeted therapy alone in advanced liver cancer: a comparative effectiveness and efficacy prediction study

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2300073556
Enrollment
Unknown
Registered
2023-07-14
Start date
2023-07-15
Completion date
Unknown
Last updated
2023-07-16

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

liver cancer

Interventions

TACE combined with TKI plus PD-1 immunotherapy group:N/A
TKI plus PD-1 group:N/A

Sponsors

Chinese PLA General Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 75 Years

Inclusion criteria

Inclusion criteria: 1) Clinical or pathological diagnosis of primary liver cancer; 2) BCLC-C stage liver cancer; 3) Both genders, aged 18-75; 4) Received targeted plus immunotherapy or TACE combined with targeted plus immunotherapy; 5) Complete baseline imaging and laboratory data; 6) Completed at least one imaging and clinical assessment within 3 months of starting initial treatment; 7) Has complete follow-up information.

Exclusion criteria

Exclusion criteria: 1) Presence of malignant tumors in other systems of the body; 2) Impaired vital organ function, such as the heart, brain, or kidneys; 3) History of liver function classified as Child-Pugh C prior to treatment initiation, along with significant ascites, hepatic encephalopathy, or a history of esophageal variceal bleeding; 4) No prior treatment with TACE, ablation therapy, targeted therapy, immunotherapy, biologic therapy, radiation therapy, or surgical intervention before treatment initiation.

Design outcomes

Primary

MeasureTime frame
Objective Reaction Rate;overall survival;

Secondary

MeasureTime frame
Edverse Events above 3-grade;progression-free survival;

Countries

China

Contacts

Public ContactFeng Duan

Chinese PLA General Hospital

duanfeng@vip.sina.com+86 139 1098 4586

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026