RecruitingPhase 1Phase 2NCT06311851

Transarterial Chemoembolization (TACE) Plus Bevacizumab for Liver Metastases

An Open-Label Pilot Study to Evaluate Efficacy and Safety of Bevacizumab Via Transarterial Chemoembolization (TACE) in Patients With Liver Metastases


Sponsor

Pardis Noor Medical Imaging and Cancer Center

Enrollment

40 participants

Start Date

Jun 1, 2025

Study Type

INTERVENTIONAL

Conditions

Summary

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.


Eligibility

Min Age: 18 YearsMax Age: 80 Years

Inclusion Criteria7

  • Confirmation of metastatic liver cancer via histological examination or a characteristic imaging profile on dynamic computed tomography (CT) scan or magnetic resonance imaging (MRI) without indications for surgical resection
  • Eastern cooperative oncology group performance status (ECOGPS) of 0 or 1
  • Liver function categorized as Child-Pugh class A or B
  • Stable non-hepatic metastases, such as skeletal, pulmonary, or lymph node metastases
  • Hepatic tumor burden below 70%
  • Expected survival duration exceeding six months
  • Laboratory findings meeting specific criteria, including platelet count \>50×109 /L, hemoglobin \>8.0 g/dL, ANC count ≥1.5 × 109/L, bilirubin \<51 mmol/L, alanine and aspartate aminotransferase \<3 times the upper limit of the normal range, and serum creatinine \<1.5 times the upper limit of the normal range.

Exclusion Criteria5

  • Active infection
  • Presence of severe comorbidities, such as hepatic encephalopathy, refractory ascites, and esophageal variceal bleeding
  • Prior liver resection
  • Previous TACE therapy received at other healthcare facilities
  • Poor performance status (ECOGPS \> 1)

Interventions

DRUGBevacizumab

Infusion of Bevacizumab-loaded hepaspher through transarterial chemoembolization.


Locations(1)

Pardis Noor Medical Imaging and Cancer Center

Tehran, Tehran Province, Iran

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NCT06311851


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