Contrast Enhanced Ultrasound to Evaluate Response to Chemoembolization in Patients With Liver Tumors

Trial statusRecruiting
Trial phasePhase 2
Trial typeInterventional
Biological sexAll
Age18+
Sponsorjohn eisenbrey

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

266 Participants
are divided into 1 treatment group

Sponsors and collaborators

john eisenbrey

Lead sponsor

Thomas Jefferson University

Sponsor institution

National Cancer Institute (NCI)

Collaborator