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Active Not RecruitingNCT04728633

Transarterial Chemoembolization for the Treatment of Uveal Melanoma With Liver Metastases

Chemoembolization of Uveal Melanoma Hepatic Metastases Using 300mg of BCNU Dissolved in Lipiodol® Followed by Gelfoam® Embolization

Status
Active Not Recruiting
Phase
Phase 2
Study type
Interventional
Enrollment
28 (actual)
Sponsor
Thomas Jefferson University · Academic / Other
Sex
All
Age
18 Years
Healthy volunteers
Not accepted

Summary

This phase II trial studies the effect of transarterial chemoembolization in treating patients with uveal melanoma that has spread to the liver (liver metastases). Transarterial chemoembolization involves the injection of a blocking agent (gelatin sponge, ethiodized oil) and a chemotherapy agent (carmustine) directly into the artery in the liver to treat liver cancers. Chemotherapy drugs, such as carmustine, work in different ways to stop the growth of tumor cells, either by killing the cells, by stopping them from dividing, or by stopping them from spreading. transarterial chemoembolization with carmustine in combination with ethiodized oil and gelatin sponge may help cause the tumors in the liver to shrink or disappear.

Detailed description

PRIMARY OBJECTIVE: To determine the efficacy (clinical response) in terms of disease control rate (DCR) (complete response \[CR\] + partial response \[PR\] + stable disease \[SD\]) with chemoembolization of hepatic metastases with 300 mg of carmustine (BCNU) in ethiodized oil in metastatic uveal melanoma patients. SECONDARY OBJECTIVES: To investigate overall survival (OS) and progression-free survival (PFS) in uveal melanoma patients with hepatic metastases. To assess the toxicity of the above treatment regimen. OUTLINE: Patients undergo transarterial chemoembolization (TACE) by receiving an infusion of carmustine dissolved in ethiodized oil and an injection of gelatin sponge. Treatment repeats once every 4 weeks (Q4W) for bilobar disease or once every 7 weeks (Q7W) for unilobar disease in the absence of disease progression or unacceptable toxicity or until maximum clinical benefit is obtained. Steroid taper will begin the day of patient discharge. After completion of study treatment, patients are followed up at 30 days, and then every 2 months for up to 2 years. After 3 years from first treatment, follow-up scans may occur every 16-20 weeks and labs every other month.

Conditions

Interventions

TypeNameDescription
DRUGCarmustineGiven via infusion
DRUGEthiodized OilGiven via infusion
PROCEDURETransarterial ChemoembolizationUndergo TACE
OTHERMedical Device Usage and EvaluationGiven gelatin sponge via injection

Timeline

Start date
2021-09-27
Primary completion
2027-01-31
Completion
2027-06-30
First posted
2021-01-28
Last updated
2025-08-06

Locations

1 site across 1 country: United States

Regulatory

Source: ClinicalTrials.gov record NCT04728633. Inclusion in this directory is not an endorsement.