Hepatic Artery Infusion Pump Chemotherapy With Floxuridine and Dexamethasone in Combination With Systemic Chemotherapy for Patients With Colorectal Cancer Metastatic to the Liver
Part of paid clinical trials in Bethesda, Maryland.
- Sponsor
- National Cancer Institute (NCI)
- Study ID
- NCT03366155
- Phase
- PHASE2
- Status
- Completed
Conditions
- Colorectal Adenocarcinoma
- Colorectal Cancer
- Colorectal Cancer With Hepatic Metastases
- Colorectal Carcinoma
- Liver Metastases
Eligibility Criteria
- Sex
- ALL
- Age
- 18 Years - N/A
- Healthy Volunteers
- Not accepted
Interventions
- Codman 3000 constant flow pump catheter — DEVICEimplanted Medtronic SynchroMed II Pump with codman 3000 Constant Flow Pump Catheter
- Panitumumab — DRUG6 mg/kg, IV
- FUDR-Dex — DRUGHAIP will be filled with mixture of Floxuridine and Dexamethasone. Pump will perfuse drugs to liver for 14 days. Floxuridine (0.12 mg/kg X pump volume X pump flow rate),Dexamethasone (1 mg/day X pump volume (30) X pump flow rate)
- Oxaliplatin — DRUG85 mg/m2, IV
- 5FU — DRUG2000 mg/m2, IV 46-hour infusion of 5-Fluorouracil + 400 mg/m2, IV of Leucovorin
- Irinotecan — DRUG150 mg/m2, IV
- HAIP installation — PROCEDUREHAI pump installation
- cetuximab — DRUG500 mg/m2, IV
- Medtronic SynchroMed II Pump — DEVICEimplanted Medtronic SynchroMed II Pump with Codman 3000 Constant Flow Pump Catheter
Study Details
Background: Many people with colorectal cancer get liver metastases. Standard treatment for this is a combination of chemotherapy drugs. Directing the chemotherapy to the liver may be effective. A device that does this a pump that delivers drugs over 2 weeks at constant rate into the hepatic artery. The person s body temperature causes the drug to flow from the pump. Researchers want to see if this helps people with colorectal metastases to the liver. Objective: To study the effectiveness of a hepatic artery infusion pump at treating colorectal metastases to the liver. Eligibility: Adults at least 18 years old with colorectal metastases to the liver Design: Participants will be screened with: Medical history Physical exam Heart, blood, and urine tests Scans Participants will stay in the hospital a few days. A small plastic tube (catheter) will be inserted in an artery into the liver. The catheter will be attached to the pump. That will lie under the skin on the abdomen. It will be small and participants will be able to feel it. Participants will get treatment in 28-day cycles. Every Day 1, they will have physical exam, symptom review, and blood tests. Every 2 weeks, they will come to the clinic to get chemotherapy by a catheter or port. Every 12 weeks, they will have a scan. Tissue samples may be taken during the study. When they finish the drug, participants may have the pump removed. They will repeat the Day 1 tests. They will be called every 6 months to see how they are doing.
Key Dates
- Start date
- Jun 24, 2019
- Status verified
- Jan 2026
- Primary completion
- Nov 13, 2025
- Completion
- Nov 13, 2025
Study Design
- Enrollment
- 24 participants (actual)
- Allocation
- NA
- Intervention model
- SINGLE_GROUP
- Primary purpose
- TREATMENT
Arms
- Experimental: 1/ Arm 1HAIP chemotherapy + Systemic chemotherapy
Primary Outcome Measure
Response rate (RR) [ Time Frame: at progression ]
Locations (1)
| Facility | City | State | ZIP | Site coordinators |
|---|---|---|---|---|
| National Institutes of Health Clinical Center | Bethesda | Maryland | 20892 | - |
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