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Clinical study of Stereotactic Body Radiation Therapy (SBRT) combined with Tetrandrine for unresectable hepatocellular carcinoma

Clinical study of Stereotactic Body Radiation Therapy (SBRT) combined with Tetrandrine for unresectable hepatocellular carcinoma

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR-IOR-14005650
Enrollment
Unknown
Registered
2014-12-08
Start date
2014-12-01
Completion date
Unknown
Last updated
2017-04-18

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

Conditions

Unresectable Hepatocellular Carcinoma

Interventions

SBRT:Stereotactic Body Radiation Therapy (SBRT)
SBRT combined with Tetrandrine:Stereotactic Body Radiation Therapy (SBRT) combined with Tetrandrine

Sponsors

Zhongshan Hospital Fudan University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 65 Years

Inclusion criteria

Inclusion criteria: 1. age 18-75 years; 2. ECOG performance status (PS) 0-2; 3. expecting survival time longer than 3 months; 4. Patients with pathologically confirmed hepatocellular carcinoma; or had clinical features of patients with a clinical diagnosis of hepatocellular carcinoma; 5. CT, MRI and (or) B-ultrasound comfirmed unresectable hepatocellular carcinoma confined to the liver with or without portal vein tumor thrombus; 6. no history of abdominal radiotherapy; 7. adequate bone marrow-absolute neutrophil count (ANC); 1500 cells/mm3, platelet count: 100,000 cells/mm3, and hemoglobin: 10 g/dL; 8. kidney function (serum creatinine less than 115 umol/L), liver function (serum total bilirubin less than 34 umol/L) and Child-Pugh A or B; 9. Patients with intrahepatic multiple HCC and lipiodol deposition was not well after interventional therapy.

Exclusion criteria

Exclusion criteria: 1. Patients will be ruled out if inconsistent with any one of enter criterion; 2. with distant metastatic disease; 3. Patients with prior malignancy were ineligible for the study, with the exception of those who had experienced nonmelanoma skin cancer, in situ cancer of the cervix, or other cancer for which the patient had been disease free for longer than 5 yr; 4. Obstructive jaundice without external biliary drainage or patients with uncontrolled infection or diabetes mellitus; 5. had received abdominal irradiation before; 6. Poor compliance.

Design outcomes

Primary

MeasureTime frame
Tetrandrine Tablets;

Secondary

MeasureTime frame
Progression-free survival time;AFP reaction;

Contacts

Public ContactZeng Zhaochong
zeng.zhaochong@zs-hospital.sh.cn+86 13817076800

Outcome results

None listed

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