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Transarterial infusion of bevacizumab combined with TACE for the treatment of TACE-refractory HCC

Efficacy and safety of transarterial infusion of bevacizumab combined with TACE for the treatment of TACE-refractory HCC: a single-arm, prospective, multicenter study.

Status
Recruiting
Phases
Phase 4
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR-OPC-15006859
Enrollment
Unknown
Registered
2015-08-02
Start date
2015-08-01
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

Hepatocellular carcinoma

Interventions

all patients :Transarterial infusion of bevacizumab
all patients :Routine-TACE

Sponsors

The first teaching hospital of Xinjiang medical university
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 90 Years

Inclusion criteria

Inclusion criteria: 1. TACE-refractory hepatocellular carcinoma; 2. ChildPugh A/B/C, no encephalopathy and ascites and pleural effusion need treatment; 3. ECOG performance status of 0-2; 4. Measurable tumors; 5. 18 years of age or older; 6. Life expectancy of > 12 weeks; 7. Adequate hepatic and renal function: ALB>=28g/L, TBIL=50*10^9/L.

Exclusion criteria

Exclusion criteria: 1. Biliary obstruction due to tumor invasion; 2. Definite hepatic artery - portal vein fistula; 3. Extensive portal vein cancer embolus with ChildPugh C; 4. Clinically apparent central nervous system metastases or carcinomatous meningitis; 5. Uncontrolled hypertension; 6. History of hemorrhage of digestive tract four weeks ago; 7. Any contraindication of bevacizumab or oxaliplatin; 8. Pregnant or lactating women; 9. History of major operation four weeks ago; 10. Combined with other malignance.

Design outcomes

Primary

MeasureTime frame
overall survival;

Secondary

MeasureTime frame
Time to progression;Disease control rate;Tumor response rate;safety (complication and adverse event and laboratory values);

Countries

China

Contacts

Public ContactWeixin Ren
rwx1031@163.com+86 13909911031

Outcome results

None listed

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