About this trial
This phase II trial evaluates the diagnostic performance of contrast-enhanced ultrasound (CEUS) for assessing treatment response in patients undergoing transarterial chemoembolization (TACE) for liver tumors. TACE is a hepatic artery embolization technique involving the injection of a blocking agent and a chemotherapy agent to treat liver cancers. Currently, contrast enhanced magnetic resonance imaging or computed tomography are used to assess disease response 1-2 months after TACE treatment, but ultrasound may be a less expensive, earlier alternative. CEUS is an imaging procedure that uses high-frequency sound waves to generate images of the body after administering Lumason, an imaging agent used to enhance visualization of blood flow on ultrasounds. CEUS is able to be performed during the TACE procedure, making it possible to evaluate treatment response earlier than standard techniques. CEUS may be an effective method to evaluate treatment response more accurately and much earlier than current standard evaluation methods.
Eligibility criteria
Qualifiers
Scheduled for TACE therapy of a liver tumor
Be at least 18 years of age
Be medically stable
If a female of child-bearing age, must have a negative pregnancy test
Disqualifiers
Patients who are medically unstable, patients who are seriously or terminally ill, and patients whose clinical course is unpredictable
Patients with known sensitivities to the components of lumason
Trial design
Treatments tested in this trial
- Sulfur Hexafluoride Lipid Microspheres
- Contrast-Enhanced Ultrasound
- Transarterial Chemoembolization
- Medical Chart Review
Treatment groups
Sponsors and collaborators
john eisenbrey
Lead sponsor
Thomas Jefferson University
Sponsor institution
National Cancer Institute (NCI)
Collaborator