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Ipilimumab and Nivolumab

Ipilimumab and Nivolumab With SBRT in Locally Advanced Hepatocellular Cancer

  • RegistryNCT07075120
  • PhasePhase 1
  • StatusRecruiting
  • ConditionHepatocellular Carcinoma (HCC)
  • SponsorUniversity of Hawaii
How Ipilimumab and Nivolumab works1 min

The drug

What is being tested.

Immunotherapy combination (Ipilimumab and Nivolumab) targeting CTLA-4 and PD-1 pathways to enhance immune response.

High-dose radiation therapy delivered in 3-5 fractions for local control of tumors in combination with immunotherapy. Radiation dosages are based on the RTOG 1112 trial guidelines to minimize normal tissue exposure.

Additionally, stereotactic body radiotherapy (SBRT) has been shown to enhance survival and local control when combined with systemic therapies like ICIs. However, without surgery, outcomes remain suboptimal, with response rates for ICIs alone at 20-30%, and combination ICI-SBRT treatment showing slightly better results but still a high risk of progression.

The study

How the trial runs.

Hepatocellular carcinoma (HCC) is a major cause of cancer-related deaths globally, with Native Hawaiian and Pacific Islander (NHPI) populations experiencing significantly higher mortality rates compared to other groups in Hawaii. This disparity is influenced by factors such as higher prevalence of chronic hepatitis B, non-alcoholic fatty liver disease, limited access to early detection, and delayed diagnoses.

NHPI patients are also underrepresented in clinical trials, limiting the relevance of treatment advances for this population. The standard treatment for HCC is surgical resection; however, many NHPI patients present with unresectable disease. Recent advances with immune checkpoint inhibitors (ICIs), such as nivolumab and ipilimumab, have shown promise in treating advanced HCC and improving survival in previously untreatable cases.

Live record on ClinicalTrials.gov →

Eligibility

Who the study is looking for.

  • Histologically or cytologically confirmed hepatocellular cancer
  • Solitary tumor >5 cm, OR
  • Unilobar multifocal disease either with >3 tumors or one tumor >3 cm, OR
  • Bilobar disease with adequate future liver remnant, still technically resectable, OR

Inclusion criteria as written on the registry, trimmed. The full list, with exclusions, is on the live record.

For you, or someone you love

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Members also get a deeper analysis of their records and any sequencing data, including clinical trials that may fit, reviewed by a licensed physician before they receive it.

How these trials work: what Phase 1 actually is · common questions Not clinical evidence.

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