Recruiting
Phase 2

Prednisone

Sponsor:

University of Michigan Rogel Cancer Center

Code:

NCT05901519

Conditions

Hepatocellular Carcinoma

Eligibility Criteria

Sex: All

Age: 18+

Healthy Volunteers: Not accepted

Interventions

Prednisone

Study Details

Brief summary:

Patients on this study will self administer Prednisone for three days before starting Radiation Therapy (RT) and continue to take 60 mg/day during the first three fractions of RT.

Conditions

Hepatocellular Carcinoma

Study ID

NCT05901519

Start date

Feb 16, 2024

Status verified date

Mar, 2026

Completion date

Aug, 2026

Anticipated

Primary completion date

Aug, 2026

Anticipated

Eligibility Criteria

Eligibility Criteria

Sex: All

Age: 18+

Healthy Volunteers: Not accepted

Inclusion Criteria:

  • Patients with hepatocellular carcinoma are eligible for this trial. Hepatocellular carcinoma is defined as having at least one of the following:

1. Biopsy proven hepatocellular carcinoma (HCC); or
2. A discrete hepatic tumor(s) as defined by the AASLD criteria (80) - for cirrhotic patients, >1cm with arterial hypervascularity and venous or delayed phase washout on contrast enhanced CT or MRI.
  • Patients must have recovered from the acute effects of prior liver-directed therapy (e.g., RT, RFA, or TACE), and a minimum of 4 weeks must have passed since the last procedure and protocol therapy.
  • Patients must have a performance status of ≤2.
  • Patients must be 18 years of age or older.
  • Patients with at least one of the following:

1. ALBI score equal to (-1.81) or higher (worse). This value was calculated as the equivalent ALBI score for CP score equal 7 in Cousins et al study's cohort(59).
2. Lesion(s) with a cumulative treatment diameter of ≥ 4cm.
3. CP score equal to 7 or higher (worse).
  • Patients must understand and be willing to sign an informed consent form approved for this purpose by the Institutional Review Board (IRB) of the University of Michigan Medical Center indicating that they are aware of the investigational aspects of the treatment and the potential risks.

Exclusion Criteria:

  • Any serious disease, comorbidity or intercurrent illness which precludes delivery of radiation therapy, as determined by the treating investigator.
  • Any contraindication to the administration of steroids, including

  • Documented hypersensitivity to prednisone or any component of the formulation.
  • Systemic fungal infection.
  • Patients with uncontrolled infections or with chronic infections requiring antibiotics.

Infections are considered controlled if appropriate therapy has been instituted and, at the time of enrollment, no signs of progression are present. Progression of infection is defined as hemodynamic instability attributable to sepsis, new symptoms, worsening physical signs or radiographic findings attributable to infection. Persisting fever without other signs or symptoms will not be interpreted as progressing infection.

  • Uncontrolled hyperglycemia.

  • Patients with insulin -dependent diabetes.
  • Patients with decompensated liver disease, defined as: clinical ascites requiring paracentesis, hepatic encephalopathy, hepatorenal syndrome or variceal hemorrhage.
  • Active gastrointestinal bleeding within 30 days of enrollment.

Study Design

Enrollment

20 participants

Anticipated

Intervention Model

Single group

Primary purpose

Treatment

Interventions and Outcome Measures

Arms

experimental: Patients treated with Prednisone

Prednisone will be administered for three days before starting RT, and during the first three fractions of RT. Following an interim analysis of the decrease in sTNFR1 level, a decision will be made whether to administer prednisone for seven days prior to RT, and to continue for additional seven days during RT.

Interventions

Prednisone

Patients will be treated with PO prednisone, once a day, at a dose of 60 mg/day

Primary outcome measure

  • Mitigation of liver inflammation as reflected by sTNFR1 levels [ Time Frame: at baseline, day of first RT fraction, day of 3rd RT fraction and at 1-, 3- and 6-months post commencing radiation therapy ]

Central Contacts and Locations

Central contacts

Locations

Rogel Comprehensive Cancer Center

Recruiting

Ann Arbor, Michigan, United States, 48187

Principal Investigator:

Theodore Lawrence, M.D., Ph.D.

More Information

Sponsor

University of Michigan Rogel Cancer Center

Last update posted

Mar 13, 2026

Last verified

Mar, 2026

Keywords

  • Radiation Therapy
  • Prednisone

Trial information was received from ClinicalTrials.gov and was last updated on 2026-09-10. This information was provided to ClinicalTrials.gov by University of Michigan Rogel Cancer Center on 2026-03-13.