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

Study acronym: TOMCAT
StatusRecruiting
PhasePhase 2
Started2024-02-13
View on ClinicalTrials.gov ↗

Amendment history

2026-01-29
notable
Active, Not Recruiting→Recruiting Study Identification, Study Status, Oversight, Study Design, Contacts/Locations v2
Trial statusActive, Not Recruiting→Recruiting
Study sitesdetails revised at 1 of 1 site
Study titlerevised
HAI-Floxuridine, or SIRT, Combined withWith Gemox forFor Patients withWith Intra-Hepatic Cholangiocarcinoma Not Amenable to Resection (TOMCAT)
2024-12-02
notable
Recruiting→Active, Not Recruiting Study Identification, Study Status, Oversight, Study Design, Contacts/Locations v1
Trial statusRecruiting→Active, Not Recruiting
Enrollment targetestimated 800→confirmed 39
Study sitesdetails revised at 1 of 1 site
Study titlerevised
HAI-Floxuridine, or SIRT, Combined Withwith Gemox Forfor Patients Withwith Intra-Hepatic Cholangiocarcinoma Not Amenable to Resection (TOMCAT)
2024-03-08
minor
Original filing
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
Trial Details
NCT Number NCT06313203
Lead Sponsor Oslo University Hospital
Conditions Intrahepatic Cholangiocarcinoma, Chemotherapy Effect
Enrollment 39 participants
Start Date 2024-02-13
Primary Completion 2031-01 (estimated)
Study Completion 2034-01 (estimated)
Updated on ClinicalTrials.gov 2026-02-02