RecruitingPhase 2NCT06313203

HAI-Floxuridine, or SIRT, Combined With Gemox For Patients With Intra-Hepatic Cholangiocarcinoma Not Amenable to Resection (TOMCAT)

Trans-arterial Treatment of Patients With Intra-hepatic Cholangiocarcinoma Not Amenable to Resection (TOMCAT)


Sponsor

Oslo University Hospital

Enrollment

39 participants

Start Date

Feb 13, 2024

Study Type

INTERVENTIONAL

Conditions

Summary

Patients with intrahepatic cholangiocarcinoma (IHC) have relatively aggressive tumors, and the prognosis for most of these patients is dismal. Surgery is the only option that can offer potential cure, but only an estimated 20-25 % are amenable to resection. Down-staging conventional chemotherapy has a relatively low response rate (\< 50 %). Patients will be included into the respective treatment arms based on their tumour characteristics and disease stage, but also based on their ability/preferences, as HAI-FUDR/DEX requires going to Oslo every fortnight for the duration of the treatment and SIRT has some limitations regarding tumour distribution. Data from the MSKCC has suggested a clinically relevant benefit from adding intrahepatic chemotherapy to systemic therapy. HAI-FUDR/DEX is not approved in Norway and can only be evaluated in a protocolized trial. Given the risk of distant disease progression with IHC, the addition of conventional systemic chemotherapy makes good clinical sense, and data from MSKCC supports this approach. SIRT is another modality also applied trans-arterially and directly into the tumour. This treatment is approved in Norway and available in Bergen and in Oslo. It is far less cumbersome to deliver and maintain than HAI-FUDR/DEX. The efficacy and safety of the two treatment groups, HAI-FUDR/DEX and SIRT, will be compared in a parallel cohort (non-randomized) design


Eligibility

Min Age: 18 Years

Plain Language Summary

Simplified for easier understanding

This study (called TOMCAT) is testing two different liver-directed treatments combined with chemotherapy for patients with bile duct cancer (cholangiocarcinoma) inside the liver that cannot be surgically removed. The two approaches being compared are hepatic artery infusion (delivering chemo directly to the liver's blood supply) and SIRT (tiny radioactive beads injected into liver tumors). **You may be eligible if...** - You have confirmed intra-hepatic cholangiocarcinoma (bile duct cancer inside the liver) - Your cancer cannot be removed with surgery (due to tumor size/location, multiple tumors, recurrence after prior surgery, or lymph node involvement) - Your cancer is confined to the liver or has only limited, treatable lymph node spread near the liver - You have at least one tumor measuring over 2 cm that can be measured on scans - You have not received prior chemotherapy for this cancer **You may NOT be eligible if...** - Your cancer has spread widely beyond the liver - You have already received systemic chemotherapy for this condition - Your overall health or organ function does not allow chemotherapy Talk to your doctor to see if this trial is right for you.

This summary was AI-generated to explain the trial in plain language. It is not medical advice. Always discuss eligibility with your doctor before enrolling in a clinical trial.

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Interventions

DRUGFloxuridine

A laparotomy will be performed and a catheter placed in the hepatic artery Connected to a subcutaneous pump. This pump will be percutaneously filled with Floxuridine 6 times in 2 weeks cycles, alternating with heparin-solution. The patients in this arm will also be given GemOX as systemic chemotherapy

PROCEDURESelective Internal Radiation Therapy (SIRT)

Radioactive Yttrium 90 (Y-90) labeled particles are injected selectively into the feeding arteries of the tumour(s). This allows a high radiation dose in the lesions while limiting systemic side effects.


Locations(1)

Oslo University Hospital

Oslo, Oslo, Norway

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NCT06313203


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