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
NCT Number: NCT05901519
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.
Interested in participating?
Request Info18 year and older
All sexes
Interventional
Phase 2
Ann Arbor, Michigan, 48187, United States
Location status: Recruiting
Theodore Lawrence, M.D., Ph.D.
CONTACT
Theodore Lawrence, M.D., Ph.D.
PRINCIPAL_INVESTIGATOR
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
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.
Patients will be treated with PO prednisone, once a day, at a dose of 60 mg/day
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%.
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.
Time frame: up to 6 weeks from start of study treatment
Successful completion of steroid treatment.
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.
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.
Time frame: up to 6 months from start of study treatment
assessing tumor response as part of standard of care to determine response rate
Contact information is provided by the study sponsor or research team.
University of Michigan Rogel Cancer Center
Other
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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