Actively Recruiting

Phase 1
Phase 2
Age: 18Years - 80Years
All Genders
NCT06311851

Transarterial Chemoembolization (TACE) Plus Bevacizumab for Liver Metastases

Led by Pardis Noor Medical Imaging and Cancer Center · Updated on 2025-11-25

40

Participants Needed

1

Research Sites

47 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

Trans arterial chemoembolization (TACE) has emerged as a treatment option for chemotherapy-refractory diseases in Liver metastases. By delivering chemotherapy agents directly to the tumor site, TACE can maximize local drug concentrations and reduce systemic adverse reactions. Bevacizumab is a monoclonal antibody that functions as an angiogenesis inhibitor. It works by slowing the growth of new blood vessels by inhibiting vascular endothelial growth factor A (VEGF-A). The application of Bevacizumab during TACE has not been reported. In this study, we will evaluate the the overall survival (OS)、efficacy, and safety of the application of Bevacizumab during TACE in patients with Liver Metastases by designing an open, single-arm phase II clinical study.

CONDITIONS

Official Title

Transarterial Chemoembolization (TACE) Plus Bevacizumab for Liver Metastases

Who Can Participate

Age: 18Years - 80Years
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Confirmed metastatic liver cancer by biopsy or characteristic imaging with no option for surgery
  • ECOG performance status of 0 or 1
  • Liver function classified as Child-Pugh class A or B
  • Stable non-liver metastases such as bone, lung, or lymph nodes
  • Liver tumor burden less than 70%
  • Expected survival longer than 6 months
  • Laboratory results with platelet count >50 x10^9/L, hemoglobin >8.0 g/dL, ANC ≥1.5 x10^9/L, bilirubin <51 mmol/L, ALT and AST less than 3 times upper normal limit, serum creatinine <1.5 times upper normal limit
Not Eligible

You will not qualify if you...

  • Active infection
  • Severe health problems including hepatic encephalopathy, refractory ascites, or esophageal variceal bleeding
  • Previous liver surgery
  • Prior TACE treatment at other centers
  • Poor performance status with ECOG > 1

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 1 location

1

Pardis Noor Medical Imaging and Cancer Center

Tehran, Tehran Province, Iran, 021

Actively Recruiting

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Research Team

S

Shahram Akhlaghpoor, M.D

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

NONE

Allocation

NA

Model

SINGLE_GROUP

Primary Purpose

TREATMENT

Number of Arms

1

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