RecruitingPhase 2NCT06858735
HYPERION CCA: a Phase 2 Trial of Systemic Therapy With or Without Liver-directed Radiation Therapy for Patients With Advanced Intrahepatic Cholangiocarcinoma
Sponsor
M.D. Anderson Cancer Center
Enrollment
60 participants
Start Date
Jun 10, 2025
Study Type
INTERVENTIONAL
Conditions
Summary
This study will compare outcomes for M1 iCCA patients treated with and without L-RT by reviewing iCCA patients found to have M1 disease at initial diagnosis at a single institution between 2010 and 2021 who received L-RT.
Eligibility
Min Age: 18 Years
Plain Language Summary
Simplified for easier understanding
This Phase 2 study is testing whether adding targeted liver radiation therapy to standard systemic drug treatment improves outcomes for patients with advanced intrahepatic cholangiocarcinoma (a type of liver bile duct cancer).
**You may be eligible if...**
- You are 18 or older with a confirmed diagnosis of intrahepatic cholangiocarcinoma (bile duct cancer within the liver)
- You have at least one liver tumor measuring 3 cm or more
- Your cancer is either unresectable (cannot be surgically removed) or has spread beyond the liver
- You weigh more than 30 kg
**You may NOT be eligible if...**
- You are currently enrolled in another interventional clinical trial
- You have unresolved significant side effects (Grade 2 or higher) from prior cancer treatment
- You have active nerve damage (Grade 2 or higher neuropathy)
- You have serious heart, liver, or kidney problems
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
DRUGDurvalumab
Given by IV
DRUGGemcitabine
Given by IV
DRUGCisplatin
Given by IV
Locations(1)
View Full Details on ClinicalTrials.gov
For the most up-to-date information, visit the official listing.
NCT06858735