Atezolizumab in Combination With a Multi-Kinase Inhibitor for the Treatment of Unresectable, Locally Advanced, or Metastatic Liver Cancer (NCT05168163)
A Phase II Randomized Study of Atezolizumab Plus Multi-Kinase Inhibitor Versus Multi-Kinase Inhibitor Alone in Subjects With Unresectable, Advanced Hepatocellular Carcinoma Who Previously Received Atezolizumab Plus Bevacizumab
๐ฉบ Plain-English Summary (8th-Grade Level)
This phase II trial tests whether atezolizumab in combination with a multi-kinase inhibitor (cabozantinib or lenvatinib) compared to multi-kinase inhibitor alone in treating patients with liver cancer that cannot be removed by surgery (unresectable), has spread to has spread to nearby tissue or lymph nodes (locally advanced), or has spread to other places in the body (metastatic), for which the patient has received treatment in the past (previously treated). Immunotherapy with monoclonal antibodies, such as atezolizumab, may help the body's immune system attack the cancer, and may interfere with the ability of tumor cells to grow and spread. Cabozantinib and lenvatinib may stop the growth of tumor cells by blocking some of the enzymes needed for cell growth. Giving atezolizumab with cabozantinib or lenvatinib may kill more tumor cells in patients with liver cancer.
Who can join: Review the eligibility criteria below.
Location: Mayo Clinic in Arizona โ Scottsdale, Arizona
Age range: 18 Years
๐งช Interventions in This Study
๐ "Do I Qualify?" โ 1-Minute Self Screener
Instant ChecklistFull eligibility criteria are available on the official NIH protocol. View the criteria โ
๐ All Participating Trial Locations (16 Sites)
- Mayo Clinic in Arizona โ Scottsdale, Arizona
- Mayo Clinic in Florida โ Jacksonville, Florida
- Cleveland Clinic Weston Florida โ Weston, Florida
- University of Chicago Comprehensive Cancer Center โ Chicago, Illinois
- Carle Cancer Center NCI Community Oncology Research Program โ Urbana, Illinois
- University Medical Center New Orleans โ New Orleans, Louisiana
- Michigan Cancer Research Consortium NCORP โ Ann Arbor, Michigan
- University of Michigan Comprehensive Cancer Center โ Ann Arbor, Michigan
- Mayo Clinic in Rochester โ Rochester, Minnesota
- Roswell Park Cancer Institute โ Buffalo, New York
- Duke University Medical Center โ Durham, North Carolina
- University Hospitals Cleveland Medical Center โ Cleveland, Ohio
- Allegheny General Hospital โ Pittsburgh, Pennsylvania
- Rapid City Regional Hospital โ Rapid City, South Dakota
- Froedtert and the Medical College of Wisconsin LAPS โ Milwaukee, Wisconsin
- Medical College of Wisconsin โ Milwaukee, Wisconsin
๐ Contact the Study Coordinator
Phone: (480) 342-3256
Email: mihalik.laurie@mayo.edu
Coordinator details come directly from the registered NIH protocol. Confirm the study is still recruiting before traveling.
๐ฐ Cost, Insurance & Patient Rights
- 100% Free Items: The investigational treatment and protocol-required procedures are supplied at zero cost by the sponsor.
- Routine Patient Care: Under federal law (ACA ยง 2709) and many state statutes, routine care costs are covered during participation.
- Voluntary Participation: You may withdraw at any time without affecting your standard medical care.
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๐ก How to Participate
- Check the checklist above to see if you may qualify.
- Contact the study coordinator using the phone/email above.
- Ask about the visit schedule, what is covered at no cost, and any travel support.
- Confirm with your own doctor before making a decision.