Sequential treatment of Regorafenib and immunotherapy after chemotherapy for advanced liver cancer

Observation Study of Sequential Regorafenib Combined With Immunocheckpoint Inhibitors After Hepatic Artery Infusion Chemotherapy for Advanced Hepatocellular Carcinoma

This study is testing if giving Regorafenib and immune therapy after chemotherapy can help people with advanced liver cancer who can't have other local treatments.

Quick facts

• Study type: Observational
• Enrollment: 50 (estimated)
• Ages: 18 Years to 75 Years
• Sex: All
• Sponsor: Sun Yat-sen University (Academic / other)
• Drugs / interventions: radiation, prednisone, chemotherapy
• Locations: 2 sites (Guangzhou, Guangdong and 1 other locations)
• Trial ID: NCT05573282 on ClinicalTrials.gov

What this trial studies

This observational study evaluates the efficacy and safety of sequential therapies combining Regorafenib and immune checkpoint inhibitors (ICIs) in patients with advanced hepatocellular carcinoma (HCC) who have completed 4-6 cycles of hepatic arterial infusion chemotherapy (HAIC). The study aims to identify patients who are not suitable for loco-regional therapies after HAIC and assess their response to the sequential treatment. Patients will receive Regorafenib daily and ICIs intravenously, starting no earlier than 30 days after their last HAIC cycle. The study will monitor treatment outcomes and safety profiles to provide insights into this therapeutic approach.

Who should consider this trial

Good fit: Ideal candidates are patients with advanced unresectable or metastatic HCC who have completed 4-6 cycles of HAIC and are not suitable for further loco-regional therapies.

Not a fit: Patients with early-stage liver cancer or those who have not undergone HAIC treatment may not benefit from this study.

Why it matters

Potential benefit: If successful, this approach could improve treatment outcomes for patients with advanced HCC who have limited options after chemotherapy.

How similar studies have performed: While the combination of Regorafenib and ICIs has shown promise in other studies, this specific sequential approach following HAIC is relatively novel.

Eligibility criteria

Inclusion Criteria:

Written informed consent must be obtained prior to any screening procedures.

* Cytohistological confirmation is required for diagnosis of HCC.
* Patients with advanced (unresectable and/or metastatic, stage C based on Barcelona-Clinic Liver Cancer \[BCLC\] staging classification) hepatocellular carcinoma who have completed 4-6 cycles HAIC. Treated efficacy evaluation has confirmed that these patients are not suitable for loco-regional therapies or surgical resection.
* At least one tumor lesion meeting measurable disease criteria as determined by RECIST v1.1. Lesions previously treated with local therapy, such as radiation therapy, hepatic arterial embolization, radiofrequency ablation, and percutaneous interventional therapy should not be selected unless progression is noted at baseline, in which case, these lesions would be considered as non-target lesions.
* Current cirrhotic status of Child-Pugh class A-B, with no encephalopathy. Ascites controlled by diuretics is permitted in this study.
* Availability of a representative tumor tissue specimen (archival tumor tissue is allowed) at pre-screening.
* Eastern Cooperative Oncology Group Scale for Assessment of Patient Performance Status ≤ 2.
* Both men and women enrolled in this trial must use adequate barrier birth control measures during the course of the trial and 4 weeks after the completion of trial.
* Adequate bone marrow, liver and renal function as assessed by central lab by means of the following laboratory requirements from samples within 7 days prior to procedure:
* Hemoglobin \> 100g/L
* Absolute neutrophil count \>3.0 ×109/L
* Neutrophil count \> 1.5 ×109/L
* Platelet count ≥ 50.0 ×109/L
* Total bilirubin \< 51 μmol/L
* Alanine transaminase (ALT) and aminotransferase (AST) \< 5 x upper limit of normal
* Albumin \> 28 g/L
* Prothrombin time (PT)-international normalized ratio (INR) \< 2.3, or PT \< 6 seconds above control
* Serum creatinine \< 110 μmol/L
* Willing and able to comply with scheduled visits, treatment plan and laboratory tests.

Exclusion Criteria:

* A history of liver decompensation, such as refractory ascites, gastrointestinal bleeding, or hepatic encephalopathy; Uncontrolled complications, including but not limited to: Persistent or activity (except the HBV and HCV) infection, symptoms of congestive heart failure and uncontrolled diabetes, uncontrolled hypertension, unstable angina, uncontrolled arrhythmias, active ILD, severe chronic GI disease accompanied by diarrhea, or compliance with requirements may limit the research, resulted in significant increase risk of AE or influence Subjects provided psychiatric/social problem status on their ability to provide written informed consent. A history of active primary immunodeficiency or human immunodeficiency virus; Active or previous records of autoimmune disease or inflammatory diseases, including inflammatory bowel disease (e.g., colitis or Crohn's disease\], diverticulitis, except \[diverticulosis\], systemic lupus erythematosus (SLE), sarcoidosis syndrome or Wegener syndrome (e.g., granulomatous vasculitis, gray's disease, rheumatoid arthritis, the pituitary gland inflammation and uveitis\]).
* Known to produce allergic or hypersensitive reactions to any study drug or any excipient thereof;
* Significant clinical gastrointestinal bleeding or a potential risk of bleeding was identified by the investigator during the 30 days prior to study entry.
* Tumors of the central nervous system, including metastatic brain tumors;
* Pregnant women or breast-feeding patients;
* Complicated with other malignant tumors:
* Malignant tumors that have been treated for therapeutic purposes, have no known active disease for 5 years prior to the first administration of the study drug, and have a low potential risk of recurrence.
* Fully treated non-melanoma skin cancer or malignant freckle moles with no evidence of disease.
* Fully treated carcinoma in situ without evidence of disease.
* Prior to the initial dosing of the study drug, they had received anti-PD-1, anti-PD-L1, or anti-CTLA-4 therapy.
* Has received anti-tumor system therapy for HCC. Non-anti-tumor purpose combined hormone therapy (e.g., hormone replacement therapy) is excluded.
* Is currently using, or has used an immunosuppressive drug within 14 days prior to the first dose of the investigational drug. This standard has the following exceptions:
* intranasal, inhaled, topical or topical steroids. (e.g., intraarticular)
* Systemic corticosteroid therapy not exceeding 10 mg/ day of prednisone or its physiological equivalent as a prophylactic use of steroids for hypersensitivity. (e.g., CT scan pretherapy medication)
* Steroids as a prophylactic for allergic reactions.
* A live attenuated vaccine was administered within 30 days prior to the first administration of the study drug. Note: If enrolled, patients shall not receive live attenuated vaccine within 30 days of receiving study drug therapy and after the last administration of study drug.
* Uncontrolled hypertension: systolic pressure ≥ 160 mmHg or diastolic pressure ≥ 100 mmHg despite anti-hypertension medications ≤ 28 days before randomization or first dose of drug.
* Pregnant or lactating women, or fertile men or women who do not want to use high-efficiency contraceptives, 6 months after the last dosing of study treatment, from screening to study treatment. Based on the patient's preferred and customary lifestyle, abstinence during treatment and washout is an acceptable contraceptive method.

Where this trial is running

Guangzhou, Guangdong and 1 other locations

• Department of Minimally Invasive and Interventional Radiology, Liver Cancer Study and Service Group, Sun Yat-sen University Cancer Center, — Guangzhou, Guangdong, China (Recruiting)
• Sun Yat-sen University Cancer Center — Guanzhou, Guangdong, China (Recruiting)

Study contacts

• Principal investigator: Ming Zhao, M.D. & Ph.D. — Department of Minimally Invasive and Interventional Radiology, Liver Cancer
• Study coordinator: Ming Zhao, M.D. & Ph.D.

Conditions Hepatocellular Carcinoma; Hepatic arterial infusion chemotherapy; Regorafenib; Immunocheckpoint inhibitor