Skip to content

A clinical trial for SBRT combined with PD-1 monoclonal antibody in the treatment of unresectable hepatocellular carcinoma

A clinical trial for SBRT combined with PD-1 monoclonal antibody in the treatment of unresectable hepatocellular carcinoma

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR1800020454
Enrollment
Unknown
Registered
2018-12-30
Start date
2019-01-01
Completion date
Unknown
Last updated
2019-01-14

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

Conditions

unresectable hepatocellular carcinoma

Interventions

Group 1:SBRT combined with PD-1 monoclonal antibody group

Sponsors

Union Hospital, Tongji Medical College, Huazhong University of Science and Technology
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 75 Years

Inclusion criteria

Inclusion criteria: 1. Aged 18 to 75 years old; 2. The patient was diagnosed as hepatocellular carcinoma for the first time; 3. Patients with locally advanced liver cancer who are unwilling or unwilling to undergo liver transplantation, hepatectomy, arterial chemoembolization and radiofrequency therapy must be diagnosed on the basis of biopsy or typical imaging findings (previous history of cirrhosis or chronic hepatitis B and hepatitis C), strict Patients with primary locally advanced HCC (single lesion diameter <6 cm) who meet the clinical diagnostic criteria for primary diagnosis and treatment of primary liver cancer (2011 version) or pathologically diagnosed or cytologically untreated without systemic chemotherapy and molecular targets To treatment; 4. Child-pugh liver function rating: grade A or better grade B (no more than 8 points); 5. ECOG PS score: 0-2; 6. The main organ function is normal, which meets the following criteria: (1) blood routine examination: HB greater than or equal to 90g/L; the ANC acuity 1.5 x 10^9/L; PLT acuity 70 x 10^9/L; (2) biochemical examination: ALB greater than or equal to 28g/L; the ALT and AST uln 5 or less; TBIL ULN 1.5 or less; Cr 1.5 or less ULN; 7. The subjects volunteered to participate in this study, signed the informed consent form, followed up with good compliance.

Exclusion criteria

Exclusion criteria: 1. Poor physical condition, PS score 3-4; 2. Grade C of liver function Child; 3. Large tumor, obvious hypersplenism, hepatic encephalopathy, massive ascites or extensive abdominal metastasis; 4. Active peptic ulcer, severe esophagogastric varices.

Design outcomes

Primary

MeasureTime frame
PFS;OS;MRI;

Secondary

MeasureTime frame
AFP;Liver function;Blood routine examination;Lymphocyte subsets;

Countries

China

Contacts

Public ContactXue Jun

Union Hospital, Tongji Medical College, Huazhong University of Science and Technology

xjunion@126.com+86 15071258754

Outcome results

None listed

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