Y-90 Radioembolization + Immunotherapy for Liver Cancer

No Placebo GroupAll trial participants will receive the active study treatment (no placebo)
Prior Safety DataThis treatment has passed at least one previous human trial
Breakthrough TherapyThis drug has been fast-tracked for approval by the FDA given its high promise

What You Need to Know Before You Apply

What is the purpose of this trial?

This trial explores a new combination treatment for liver cancer that cannot be surgically removed and has spread nearby. It combines Y-90 radioembolization (a targeted radiation therapy) with three drugs: durvalumab and tremelimumab (both immunotherapy drugs) and zanzalintinib (a targeted therapy drug). The goal is to stop the cancer from growing. The trial aims to determine if this approach can effectively treat advanced liver cancer. People with liver cancer that cannot be surgically removed and who have not previously received certain treatments might be suitable candidates. As a Phase 2 trial, the research focuses on measuring the treatment's effectiveness in an initial, smaller group, offering a chance to contribute to advancements in liver cancer treatment.

Do I need to stop my current medications for the trial?

The trial protocol does not specify if you must stop taking your current medications. However, certain medications like specific anticoagulants and complementary medicines must be stopped before starting the trial. It's best to discuss your current medications with the trial team to ensure safety and compliance.

Is there any evidence suggesting that this trial's treatments are likely to be safe?

Previous studies have shown that Yttrium-90 radioembolization is safe for treating liver cancer, with usually manageable side effects. Most patients tolerate this treatment well, and serious complications are rare.

Research on durvalumab and tremelimumab indicates some risk of serious side effects. About 19% of patients experienced severe reactions within six months, and fatal reactions occurred in about 8% of cases, with 1% of deaths directly linked to the treatment.

Early data suggests that Zanzalintinib is generally well tolerated. Common side effects include diarrhea and tiredness, but these are usually manageable.

Overall, while risks exist, many patients manage these treatments well. Discuss potential side effects with a healthcare provider.12345

Why are researchers excited about this trial's treatments?

Researchers are excited about this treatment combination for liver cancer because it integrates innovative methods and therapies. Unlike standard treatments like chemotherapy and surgical resection, this approach combines Y-90 radioembolization, which directly targets the liver tumors with radiation, and immunotherapy drugs like durvalumab and tremelimumab, which boost the immune system's ability to fight cancer. Additionally, zanzalintinib, a kinase inhibitor, is included to further disrupt cancer cell growth pathways. This multi-pronged strategy may offer enhanced effectiveness and a more comprehensive attack on liver cancer compared to traditional options.

What evidence suggests that this trial's treatments could be effective for liver cancer?

This trial will evaluate a combination of treatments for liver cancer. Studies have shown that Y-90 radioembolization effectively treats advanced liver cancer, helping patients live longer and potentially making some eligible for surgery. In this trial, participants will receive Y-90 radioembolization alongside the immunotherapy treatments durvalumab and tremelimumab. Research indicates that combining durvalumab and tremelimumab can extend the lives of liver cancer patients, with some living more than five years. Additionally, zanzalintinib, another drug in this trial, has shown promise in shrinking tumors and improving survival times when used with other treatments. Together, these treatments offer hope for better outcomes for liver cancer patients.23456

Who Is on the Research Team?

AK

Adel Kardosh

Principal Investigator

OHSU Knight Cancer Institute

Are You a Good Fit for This Trial?

This trial is for adults (18+) with liver cancer (hepatocellular carcinoma) that can't be removed by surgery and has spread nearby. Participants need to have enough healthy liver left, certain liver function levels, and not have rare subtypes of the disease. Prior major treatments like surgery or ablation are allowed if the cancer came back.

Inclusion Criteria

* Participant must provide written informed consent before any study-specific procedures or interventions are performed
I am 18 years old or older.
My body weight is over 30 kilograms.
See 7 more

Timeline for a Trial Participant

Screening

Participants are screened for eligibility to participate in the trial

2-4 weeks
1 visit (in-person)

Cycle 1 Treatment

Patients receive tremelimumab and durvalumab intravenously, followed by Y-90 radioembolization

7-14 days
2 visits (in-person)

Cycle 2-12 Treatment

Patients receive durvalumab intravenously and zanzalintinib orally daily, with cycles repeating every 28 days

12 cycles of 28 days each
12 visits (in-person)

Follow-up

Participants are monitored for safety and effectiveness after treatment

100 days and every 6 months for 1 year
3 visits (in-person)

What Are the Treatments Tested in This Trial?

Interventions

  • Durvalumab
  • Tremelimumab
  • Yttrium-90 Microsphere Radioembolization
  • Zanzalintinib

Trial Overview

The study tests a combination of Y-90 radioembolization (injecting radioactive beads into the liver tumor), two immunotherapy drugs (durvalumab and tremelimumab), and zanzalintinib, which blocks tumor growth signals. The goal is to see how well this combo treats advanced, inoperable liver cancer.

How Is the Trial Designed?

1

Treatment groups

Experimental Treatment

Group I: Treatment (Y-90, tremelimumab, durvalumab, zanzalintinib)Experimental Treatment10 Interventions

Find a Clinic Near You

Who Is Running the Clinical Trial?

OHSU Knight Cancer Institute

Lead Sponsor

Trials
239
Recruited
2,089,000+

Exelixis

Industry Sponsor

Trials
126
Recruited
20,500+
Michael M. Morrissey profile image

Michael M. Morrissey

Exelixis

Chief Executive Officer since 2010

PhD in Chemistry from Harvard University, BSc in Chemistry from the University of Wisconsin

Vicki L. Goodman profile image

Vicki L. Goodman

Exelixis

Chief Medical Officer since 2022

MD

Oregon Health and Science University

Collaborator

Trials
1,024
Recruited
7,420,000+

Citations

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