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)

The University of Texas M. D. Anderson Cancer Center

Houston, Texas, United States

View Full Details on ClinicalTrials.gov

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NCT06858735


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