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Efficacy and Safety of the Combination of transarterial therapies with donafenib plus Anti-PD-1 Antibody for Unresectable Hepatocellular Carcinoma: A Retrospective Real-world study

Efficacy and Safety of the Combination of transarterial therapies with donafenib plus Anti-PD-1 Antibody for Unresectable Hepatocellular Carcinoma: A Retrospective Real-world study

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2200065637
Enrollment
Unknown
Registered
2022-11-10
Start date
2022-11-18
Completion date
Unknown
Last updated
2023-05-15

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

Conditions

hepatocellular carcinoma

Interventions

Observatoional group:transarterial therapiescombined with donafenib and Anti-PD-1 Antibody

Sponsors

Zhujiang Hospital of Southern Medical University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 75 Years

Inclusion criteria

Inclusion criteria: 1. Clinically or histopathologically diagnosed HCC; 2. Not suitable for curative surgery, or local ablation; 3. Age 18~75 years; 4. Barcelona Clinic Liver Cancer (BCLC) Stage-B or C HCC; 5. Child–Pugh score A or B7; 6. Eastern Cooperative Group (ECOG) performance status <= 1; 7. No serious heart, lung, or renal dysfunction; 8. At least 1 measurable lesion according to modified Response Evaluation Criteria in Solid Tumors (mRECIST).

Exclusion criteria

Exclusion criteria: 1. Comorbidity with other severe systemic diseases 2. Life expectancy is less than 3 months; 3. Discontinuation of treatment for personal reasons or inability to tolerate; 4. Incomplete data.

Design outcomes

Primary

MeasureTime frame
Objective Response Rate;

Secondary

MeasureTime frame
Disease Control Rate;Progression Free Survival;Overall Survival;Duration of Response;Adverse Event;

Countries

China

Contacts

Public ContactMingxin Pan

Zhujiang Hospital of Southern Medical University

pmxwxy@sohu.com+86 18928918216

Outcome results

None listed

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