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Radioembolization

Radioembolization for Liver Cancer

Phase 1
Waitlist Available
Led By Armeen Mahvash
Research Sponsored by M.D. Anderson Cancer Center
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial
Must have
Be older than 18 years old
Timeline
Screening 3 weeks
Treatment Varies
Follow Up up to 6 months
Awards & highlights
No Placebo-Only Group

Summary

This trial studies the side effects and best way to perform yttrium Y-90 radioembolization in treating patients with metastatic liver cancer.

Who is the study for?
This trial is for patients with liver cancer that has spread, who can understand and sign a consent form. It's suitable for those eligible for standard Y90 radioembolization treatment but not for patients where the cancer affects more than half of the liver.
What is being tested?
The study tests yttrium Y-90 radioembolization, which involves injecting radioactive particles into an artery to block blood flow to liver tumors. The focus is on doing this in one session to see if it's effective and more efficient.
What are the potential side effects?
Possible side effects include abdominal pain, nausea, fever, fatigue, and potential complications from radiation like damage to nearby organs or tissues.

Timeline

Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~up to 6 months
This trial's timeline: 3 weeks for screening, Varies for treatment, and up to 6 months for reporting.

Treatment Details

Study Objectives

Study objectives can provide a clearer picture of what you can expect from a treatment.
Primary study objectives
Incidence of adverse event assessed by National Cancer Institute Common Terminology Criteria for Adverse Events version 4.0
Angiogram

Awards & Highlights

No Placebo-Only Group
All patients enrolled in this study will receive some form of active treatment.

Trial Design

1Treatment groups
Experimental Treatment
Group I: Treatment (angiography, yttrium Y-90 radioembolization)Experimental Treatment7 Interventions
The first 2 patients enrolled receive standard of care diagnostic and treatment during 2 visits for approximately 6 hours each within 2-4 weeks. During the first visit, patients undergo diagnostic angiography with embolization of potential hepatoenteric collaterals, receive technetium Tc-99m albumin aggregated as a surrogate to the therapy microspheres via catheter, and undergo planar imaging. During the second visit, patients undergo a second angiography and receive yttrium Y 90 resin microspheres via arterial microcatheter. Patients then undergo single-photon emission computed tomography-computed tomography (SPECT-CT) Bremsstrahlung imaging. All subsequent patients enrolled undergo the same previously described diagnostic and treatment during 1 visit over about 8 hours.
Treatment
First Studied
Drug Approval Stage
How many patients have taken this drug
Angiography
2014
N/A
~1900
Computed Tomography
2017
Completed Phase 2
~2740
Radioembolization
2020
Completed Phase 2
~30
Single Photon Emission Computed Tomography
2008
Completed Phase 4
~320
Technetium Tc-99m Albumin Aggregated
2014
Completed Phase 2
~70

Find a Location

Who is running the clinical trial?

National Cancer Institute (NCI)NIH
13,906 Previous Clinical Trials
41,012,016 Total Patients Enrolled
104 Trials studying Liver Cancer
26,540 Patients Enrolled for Liver Cancer
M.D. Anderson Cancer CenterLead Sponsor
3,062 Previous Clinical Trials
1,800,739 Total Patients Enrolled
22 Trials studying Liver Cancer
9,398 Patients Enrolled for Liver Cancer
Armeen MahvashPrincipal InvestigatorM.D. Anderson Cancer Center
2 Previous Clinical Trials
341 Total Patients Enrolled
~0 spots leftby Jan 2025