Targeted chemotherapy pump takes fight directly to pancreatic cancer liver tumors
NCT ID NCT03856658
First seen Jul 16, 2026 · Last updated Jul 17, 2026 · Updated 1 time
Summary
This study tests whether delivering a chemotherapy drug called floxuridine directly to the liver through a surgically placed pump can better control tumors that have spread from pancreatic cancer. Participants also receive standard chemotherapy. The goal is to see if this combination can slow or stop liver tumor growth and improve survival.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- floxuridine delivered via a hepatic artery infusion pump
- What this could lead to
- If successful, this approach could improve control of liver metastases and extend survival for people with pancreatic cancer that has spread to the liver.
- What could go wrong
- This is a small, early-phase study, so results may not apply broadly. The treatment involves surgery and carries risks such as infection, liver damage, or complications from the pump.
This is an AI summary of the original study and may miss details. Read our disclaimer.
Study facts
What this study's own registry entry says, in plain language.
- Phase
-
Phase 2
Tests whether the treatment actually works, and watches for side effects, in a larger group.
- Participants
-
14 people
The number who actually took part.
- Started
-
Feb 2019
- Expected to finish
-
Dec 2028
An estimate. End dates often move.
- Lead sponsor
-
Other sponsor
The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
- Ages
-
18 to 75 years
- Sex
-
Anyone
- Healthy volunteers
-
Not accepted
This study is not open to healthy volunteers. The entry requirements below say who it is open to.
Show the full entry requirements Hide the full entry requirements
Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion Criteria: * Biopsy-proved pancreatic adenocarcinoma with synchronous liver metastases * Elevated Cancer Antigen 19-9 (CA19-9) at diagnosis (\>37 U/mL) * Ages 18-75 years * Karnofsky performance status ≥70 * Ability to undergo general anesthesia and HAI pump placement procedure * CT or MRI scan imaging of the abdomen demonstrating accessibility of the gastroduodenal artery within 2 months of enrollment * Received a minimum of 2 months of systemic chemotherapy with stable tumor markers and imaging. Exclusion Criteria: * Primary tumor resected * Model for End Stage Liver Disease (MELD) score \>20, using the variables of: Bilirubin, serum Sodium, International Normalized Ratio (INR), serum Creatinine, and Dialysis twice in the past week. * Greater than 60% liver parenchymal involvement by tumor * Evidence of peritoneal metastases * Current alcohol abuse * Pregnant or lactating women
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Conditions
The condition(s) this trial relates to.
As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
Contacts and locations
Locations
-
Corewell Health West
Grand Rapids, Michigan, 49503, United States
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