RecruitingPhase 1NCT06058663

Radioembolization With Tremelimumab and Durvalumab for Locally Advanced Unresectable or Oligo-Metastatic Intrahepatic Cholangiocarcinoma

Phase 1 Trial of Safety and Preliminary Efficacy of Segmental Ablative Radioembolization in Combination With Tremelimumab Plus Durvalumab (MEDI4736) in Patients With Unresectable, or Oligo-Metastatic Cholangiocarcinoma Who Are Not Candidates for Curative Therapy (RAIDEN Trial)


Sponsor

Mayo Clinic

Enrollment

16 participants

Start Date

Jun 6, 2024

Study Type

INTERVENTIONAL

Conditions

Summary

This phase I trial tests the safety and side effects of yttrium-90 (Y90) radioembolization combined with immunotherapy drugs tremelimumab and durvalumab in treating patients with intrahepatic cholangiocarcinoma (cancer of the bile ducts in the liver) that has spread to nearby tissue or lymph nodes (locally advanced) and cannot be removed by surgery (unresectable) who are not candidates for curative therapy or that has spread from where it first started (primary side) to multiple other places in the body (oligo-metastatic). Cholangiocarcinoma is a rare but aggressive cancer with limited curative options outside of surgery. Immunotherapy has shown modest benefit in hepatobiliary (liver, bile ducts, and gallbladder) cancers including cholangiocarcinoma. Radioembolization is a type of radiation therapy used to treat liver cancer that is advanced or has come back where tiny beads that hold the radioactive substance (radioisotope) yttrium Y90 are injected into or near the hepatic artery (the main blood vessel that carries blood to the liver). The beads collect in the tumor and the Y90 gives off radiation. This destroys the blood vessels that the tumor needs to grow and kills the tumor cells. A monoclonal antibody is a type of protein that can bind to certain targets in the body, such as molecules that cause the body to make an immune response (antigens). Immunotherapy with monoclonal antibodies, such as durvalumab and tremelimumab, may help the body's immune system attack the cancer, and may interfere with the ability of tumor cells to grow and spread. Giving Y90 radioembolization in combination with tremelimumab and durvalumab immunotherapy may be safe and beneficial in treating patients with locally advanced, unresectable or oligo-metastatic intrahepatic cholangiocarcinoma who are not candidates for curative therapy.


Eligibility

Min Age: 18 Years

Plain Language Summary

Simplified for easier understanding

This trial is testing a combination of two immunotherapy drugs (tremelimumab and durvalumab) together with a targeted liver procedure called radioembolization for a rare type of liver cancer called intrahepatic cholangiocarcinoma (bile duct cancer in the liver). **You may be eligible if...** - You are 18 or older and weigh more than 30 kg - You have been diagnosed with bile duct cancer in the liver that cannot be removed by surgery, transplant, or ablation - Your cancer has spread to only a limited number of sites outside the liver (3 or fewer lymph nodes, or one other organ with a single lesion) - Your liver is functioning well enough **You may NOT be eligible if...** - Your cancer has spread widely outside the liver - You have conditions that make liver-directed treatment unsafe - You have received prior immunotherapy 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

PROCEDUREAngiography

Undergo mapping angiography

PROCEDUREBiopsy

Undergo biopsy

PROCEDUREBiospecimen Collection

Undergo blood sample collection

PROCEDUREComputed Tomography

Undergo CT

BIOLOGICALDurvalumab

Given IV

PROCEDUREMagnetic Resonance Imaging

Undergo MRI

PROCEDUREPositron Emission Tomography

Undergo PET/CT

BIOLOGICALTremelimumab

Given IV

PROCEDUREYttrium-90 Microsphere Radioembolization

Receive transarterial Y90 radioembolization


Locations(1)

Mayo Clinic in Florida

Jacksonville, Florida, United States

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NCT06058663


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