Stage III Hepatocellular Carcinoma AJCC v8 Clinical Trial
Official title:
Neoadjuvant Regorafenib Plus Durvalumab (MEDI4736) in Patients With High-Risk Hepatocellular Carcinoma
This phase II trial tests whether regorafenib and durvalumab work to shrink tumors in patients with high-risk liver cancer. Regorafenib may stop the growth of tumor cells by blocking some of the enzymes needed for cell growth. Immunotherapy with monoclonal antibodies, such as durvalumab, may help the body's immune system attack the cancer and may interfere with the ability of tumor cells to grow and spread. Giving regorafenib and durvalumab may work better in treating patients with high-risk liver cancer.
PRIMARY OBJECTIVE: I. To assess the overall response rate (ORR) at 16 weeks post registration. SECONDARY OBJECTIVES: I. To assess the rate of patients who undergo surgery during the course of the study. II. To assess the safety and tolerability of the combination therapy of regorafenib plus durvalumab. III. To assess the effect of combination therapy on overall survival. IV. To assess the effect of combination therapy on progression-free survival (PFS) in patients that do not undergo resection. V. To assess the effect of combination therapy on recurrent-free survival (RFS) in patients that have resection. VI. To assess the rate of pathologic complete response. CORRELATIVE RESEARCH OBJECTIVE: I. Analyze the effect of regorafenib and durvalumab on immune biomarkers in the tumor microenvironment and systemic circulation. OUTLINE: Patients receive regorafenib orally (PO) once daily (QD) on days 1-21 and durvalumab intravenously (IV) on day 1. Treatment repeats every 28 days for a maximum of 2 years from registration or until decision to proceed to surgery, disease progression, excessive toxicity, or patient withdrawal. After completion of study treatment, patients are followed every 90 days for 3 years. ;
Status | Clinical Trial | Phase | |
---|---|---|---|
Recruiting |
NCT03942328 -
Modified Immune Cells (Autologous Dendritic Cells) and a Vaccine (Prevnar) After High-Dose External Beam Radiation Therapy in Treating Patients With Unresectable Liver Cancer
|
Phase 1/Phase 2 | |
Terminated |
NCT03695250 -
BMS-986205 and Nivolumab as First or Second Line Therapy in Treating Patients With Liver Cancer
|
Phase 1/Phase 2 | |
Active, not recruiting |
NCT03896646 -
Radioembolization for HCC Patients With Personalized Yttrium-90 Dosimetry for Curative Intent (RAPY90D)
|
N/A | |
Active, not recruiting |
NCT04514484 -
Testing the Combination of the Anti-cancer Drugs XL184 (Cabozantinib) and Nivolumab in Patients With Advanced Cancer and HIV
|
Phase 1 | |
Recruiting |
NCT05168163 -
Atezolizumab in Combination With a Multi-Kinase Inhibitor for the Treatment of Unresectable, Locally Advanced, or Metastatic Liver Cancer
|
Phase 2 | |
Recruiting |
NCT05269381 -
Personalized Neoantigen Peptide-Based Vaccine in Combination With Pembrolizumab for Treatment of Advanced Solid Tumors
|
Phase 1/Phase 2 | |
Recruiting |
NCT05791448 -
AU409 for the Treatment of Advanced Primary Liver Cancers or Solid Tumor With Liver Metastatic Disease
|
Phase 1 | |
Active, not recruiting |
NCT04175912 -
Testing the Combination of Pevonedistat With Chemotherapy for Bile Duct Cancer of the Liver
|
Phase 2 | |
Recruiting |
NCT04022746 -
An Investigational Scan (Magnetic Resonance Elastography) in Detecting Treatment Response in Patients With Advanced Liver Cancer
|
N/A | |
Recruiting |
NCT05176223 -
68Ga PSMA PET Imaging for the Treatment of Advanced Liver Cancer
|
Phase 2 | |
Recruiting |
NCT05199285 -
A Phase II Study of Nivolumab + Ipilimumab in Advanced HCC Patients Who Have Progressed on First Line Atezolizumab + Bevacizumab
|
Phase 2 | |
Suspended |
NCT04380545 -
Nivolumab, Fluorouracil, and Interferon Alpha 2B for the Treatment of Unresectable Fibrolamellar Cancer
|
Phase 1/Phase 2 | |
Recruiting |
NCT04430452 -
Hypofractionated Radiotherapy Followed by Durvalumab With or Without Tremelimumab for Liver Cancer After Progression on PD-1 Inhibition
|
Phase 2 | |
Withdrawn |
NCT05157451 -
Y-90 Versus SBRT for Inoperable HCC
|
Phase 2 | |
Completed |
NCT01176604 -
Yttrium Y 90 Glass Microspheres in Treating Patients With Unresectable Hepatocellular Carcinoma
|
N/A | |
Recruiting |
NCT04605731 -
Durvalumab and Tremelimumab After Radioembolization for the Treatment of Unresectable, Locally Advanced Liver Cancer
|
Phase 1 | |
Active, not recruiting |
NCT04805788 -
Stereotactic Body Proton Radiotherapy for the Treatment of Liver Cancer
|
Phase 2 | |
Recruiting |
NCT05092373 -
Phase I Study of Tumor Treating Fields (TTF) in Combination With Cabozantinib or With Pembrolizumab and Nab-Paclitaxel in Patients With Advanced Solid Tumors Involving the Abdomen or Thorax
|
Phase 1 | |
Recruiting |
NCT05103904 -
Lenvatinib for the Treatment of Recurrent Hepatocellular Carcinoma After Liver Transplant
|
Phase 2 | |
Active, not recruiting |
NCT03439891 -
Sorafenib and Nivolumab in Treating Participants With Unresectable, Locally Advanced or Metastatic Liver Cancer
|
Phase 2 |