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NCT Number: NCT05901519

A Pilot Study of Liver Protection Using Prednisone for Patients Receiving Stereotactic Body Radiation Therapy for Hepatocellular Carcinoma

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.

Recruiting

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Key information

Age range

18 year and older

Sex eligibility

All sexes

Study type

Interventional

Phase

Phase 2

Primary location

Rogel Comprehensive Cancer Center

Ann Arbor, Michigan, 48187, United States

Location status: Recruiting

Location contact

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

CONTACT

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

PRINCIPAL_INVESTIGATOR

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Patients with hepatocellular carcinoma are eligible for this trial. Hepatocellular carcinoma is defined as having at least one of the following:
  • Biopsy proven hepatocellular carcinoma (HCC); or
  • 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:
  • 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).
  • Lesion(s) with a cumulative treatment diameter of ≥ 4cm.
  • 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.

Treatment and study plan

Prednisone

Drug

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

Primary outcomes

  1. 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

    Measuring whether sTNFR1 level is attenuated following prednisone treatment, given before and during radiation therapy for HCC patients who are at high risk of radiation induced liver toxicity. sTNFR1 levels will be summarized descriptively at each time point as absolute values and change from baseline (prior to taking prednisone). Longitudinal regression models will be used to test whether mean changes over time are statistically significant. Treatment with prednisone will be considered successful if it causes a decrease in the level of sTNFR1 of 50%, which would be predicted to decrease toxicity by 15%.

Secondary outcomes

  1. Estimating the safety of the steroid treatment

    Time frame: up to 6 weeks from start of study treatment

    Define steroid administration protocol based on the rate of drug-related grade 3-5 adverse events attributable to the study drug and experienced within the first 6 weeks of study treatment. These will be assessed via NCI's CTCAE version 5.0. Toxicity rates for patients on this study will be compared to a propensity matched historical control cohort of recently treated patients at UM who were not treated with prednisone.

  2. Percent of patients who complete of the proposed steroid treatment

    Time frame: up to 6 weeks from start of study treatment

    Successful completion of steroid treatment.

  3. Evaluate whether steroid treatment reduces radiation-induced liver toxicity

    Time frame: up to 6 weeks from start of study treatment

    Rate of liver decompensation (as measured by worsening in ALBI score>0.5) or grade 3-5 GI bleeding during the subsequent 6 months following radiation treatment. The former are laboratory values that are already collected as part of standard of care. The latter will be assessed via the NCI CTCAE version 5.

  4. Assess whether steroids have a durable ability to attenuate the level of inflammation as reflected by sTNFR1 level

    Time frame: up to 6 months from start of study treatment

    Determining the mitigation of the inflammatory state, as reflected by biomarkers previously proposed in the literature to correlate with radiation-induced liver injury.

  5. Assess tumor response

    Time frame: up to 6 months from start of study treatment

    assessing tumor response as part of standard of care to determine response rate

Study contacts

Contact information is provided by the study sponsor or research team.

Theodore Lawrence

CONTACT

[email protected]

7346479955

Sponsors and collaborators

Lead sponsor

University of Michigan Rogel Cancer Center

Other

Registry information

Important dates

Study start
2024
Primary completion
2026
Study completion
2026
First posted
Jun 13, 2023
Registry last updated
Mar 13, 2026

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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