New study aims to predict who will benefit from liver cancer immunotherapy
NCT ID NCT07623265
First seen Jun 27, 2026 · Last updated Jun 27, 2026
Summary
This study looks at ways to personalize treatment for people with liver cancer (hepatocellular carcinoma). Researchers want to find out which patients are likely to respond to immunotherapy by testing their tumor tissue and blood before treatment starts. The goal is to avoid giving ineffective treatments and their side effects to those who won't benefit. About 300 adults with suspected or confirmed liver cancer will participate.
This is an AI summary of the original study and may miss details. Read our disclaimer.
Study facts
What this study's own registry entry says, in plain language.
- Phase
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Not a phased trial
Phase numbers describe drug development. The registry uses this when they do not apply, as it does for trials of devices, procedures or behaviour changes, and for observational studies.
- Participants
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About 300 people
The number the study aims to enrol. It can still change while the study runs.
- Started
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Mar 2025
- Expected to finish
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Jan 2032
An estimate. End dates often move.
- Lead sponsor
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Other sponsor
The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
- Ages
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18 years and older
- Sex
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Anyone
- Healthy volunteers
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Not accepted
This study is not open to healthy volunteers. The entry requirements below say who it is open to.
Show the full entry requirements Hide the full entry requirements
Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
* General inclusion Criteria: 1. Male or female, age \> 18 years 2. Diagnosis or suspected diagnosis of hepatocellular carcinoma based on imaging * Specific inclusion criteria cohort 1 (retrospective/prospective data may be applicable): 1. Pathologically confirmed HCC 2. Treated with systemic treatment \[tyrosine kinase inhibitor (TKI) or immunotherapy (ICI)\] in the last 7 years and follow-up data (at least one imaging on treatment) available until 01/01/2025 3. Biopsy obtained between 01/01/2018 until 01/01/2025 4. Left-over tissue from previous diagnostic biopsies or resection specimens available 5. Time between biopsy and initiation of systemic treatment \< 1 year 6. Ability to sign informed consent for secondary use of archival tissue and data collection for study-specific research for patients who are alive * Specific inclusion criteria cohort 2 (aHCC \& prospective): 1. Suspicion of hepatocellular carcinoma (imaging criteria or recurrent disease of previously treated HCC) 2. Indication for tumor biopsy per standard of care 3. Eligible for systemic treatment (any) after pathological confirmation of HCC 4. Ability to sign informed consent for primary use of tissue and blood samples and data collection for study-specific research * Specific inclusion criteria cohort 3 (eHCC \& prospective): 1. Suspicion of hepatocellular carcinoma (imaging criteria or recurrent disease of previously treated HCC) 2. Indication for local treatment (resection or ablation) 3. Ability to sign informed consent for primary use of tissue and blood samples and for data collection for study-specific research Due to the observational nature of this study, participation in other (interventional) clinical trials is permitted, if biological materials can be collected per protocol. * General exclusion criteria: 1. Poor liver function and/or performance status which prohibits active treatment 2. Pathologically proven other malignancies of the liver, including primary cholangiocarcinoma or liver metastases 3. Treatment plan other than systemic treatment or local treatment (resection or ablation), such as TACE, TARE, liver transplantation
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Conditions
The condition(s) this trial relates to.
As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
How to take part
Only the study team decides who joins. These are the ways to reach them.
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The places running it
4 sites. The list below names each one and where it is.
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The official record
ClinicalTrials.gov lists the study team's own contact details, including names and phone numbers. We don't republish those.
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A doctor treating you
A doctor who knows your case can contact a study site on your behalf, and can tell you whether this study is worth pursuing at all.
Contacts and locations
Locations
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AZ Delta
RECRUITINGRoeselare, Belgium
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AZ Groeninge
RECRUITINGKortrijk, Belgium
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Jessa ziekenhuis
RECRUITINGHasselt, Belgium
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UZA
RECRUITINGAntwerp, Belgium
More trials for these conditions
Other studies related to the condition(s) this trial covers.
- Can two immunotherapy drugs make liver tumors more vulnerable to surgery?
- Saline barrier lets heat target liver tumors near the diaphragm
- Can a new PET tracer spot liver cancer more clearly?
- Can a smart drug starve liver tumors without harming healthy tissue?
- Liver size may hold key to immunotherapy response
- Can a new model forecast liver cancer in hepatitis b?