This phase II trial tests how well prednisone works to provide liver protection in patients with hepatocellular carcinoma (HCC) receiving stereotactic body radiation therapy (SBRT). The goal of SBRT for HCC is to optimize tumor control while carefully balancing the risk of toxicity, or inflammation in the liver. Previous studies have shown that a marker for inflammation called tumor necrosis factor receptor 1 (TNFR1) can be a predictor of liver injury following radiation therapy. Patients with high levels of TNFR1 have a greater chance of liver injury after radiation therapy compared to those with a low level. Prednisone is in a class of medications called corticosteroids. Taking prednisone before and during SBRT may decrease the level of TNFR1 in the blood, which would indicate decreased liver inflammation and risk of liver injury.
Additional locations may be listed on ClinicalTrials.gov for NCT05901519.
Locations matching your search criteria
United States
Michigan
Ann Arbor
University of Michigan Comprehensive Cancer CenterStatus: Active
Contact: Theodore Steven Lawrence
Phone: 734-647-9955
PRIMARY OBJECTIVE:
I. Obtain an estimate on the mitigation of liver inflammation prior to radiation treatment, as reflected by soluble (s)TNFR1 level, following prednisone treatment.
SECONDARY OBJECTIVES:
I. Obtain estimates on the safety of the steroid treatment, combined with SBRT treatment for treating liver cancer patients.
II. Establish the feasibility of the proposed steroid treatment protocol.
III. Evaluate whether steroid treatment reduces radiation-induced liver toxicity.
IV. Assess whether steroids have a durable ability to attenuate the level of inflammation, as reflected by sTNFR1 level, at different timepoints following radiation treatment and completion of steroid course.
V. Assess tumor response.
EXPLORATORY OBJECTIVE:
I. Characterize levels of other biomarkers of inflammation longitudinally over time.
OUTLINE: Patients are assigned to 1 of 2 arms.
ARM I: Patients receive prednisone orally (PO) once per day (QD) starting 3 days prior standard of care (SOC) SBRT (days -2 to 0) and continuing for 5 days during 3 radiation treatments (days 1-5). Patients receive gadoxetate disodium intravenously (IV) and undergo magnetic resonance imaging (MRI) scan, as well as computed tomography (CT) or MRI and blood sample collection throughout the study.
ARM II: Patients receive prednisone PO QD starting 7 days prior SOC SBRT (days -6 to 0) and continuing for 7 days during 3 radiation treatments (days 1-7). Patients receive gadoxetate disodium IV and undergo MRI, CT or MRI, and blood sample collection throughout the study.
After completion of study treatment, patients are followed up at 1, 3 and 6 months.
Trial PhasePhase II
Trial Typesupportive care
Lead OrganizationUniversity of Michigan Comprehensive Cancer Center
Principal InvestigatorTheodore Steven Lawrence