Surgery plus drugs may extend life in advanced liver cancer
NCT ID NCT07537959
First seen Jun 25, 2026 · Last updated Jun 27, 2026 · Updated 1 time
Summary
This study looks at whether surgically removing the main liver tumor, followed by standard immune-based drug therapy, can help people with liver cancer that has spread to other organs live longer. About 280 adults with resectable liver tumors and at least one metastasis will be randomly assigned to surgery plus drugs or drugs alone. The main goal is overall survival, with secondary measures including cancer progression and quality of life.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- primary tumor resection (surgery) plus immune-based systemic therapy
- What this could lead to
- If successful, this could show that combining surgery with standard drug therapy extends life for people with liver cancer that has spread.
- What could go wrong
- This is an early-stage trial with no results yet. Surgery carries risks like infection or bleeding, and the added benefit over drugs alone is unproven.
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 280 people
The number the study aims to enrol. It can still change while the study runs.
- Expected to start
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Apr 2026
An estimate. Start dates often move.
- Expected to finish
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Apr 2031
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 to 75 years
- 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.
Inclusion Criteria: * Age 18 to 75 years * Hepatocellular carcinoma confirmed by imaging and/or histology according to AASLD or EASL criteria * Resectable primary intrahepatic tumor with expected R0 resection * ECOG performance status 0 to 1 * At least one measurable extrahepatic metastatic lesion according to RECIST version 1.1 * Child-Pugh class A or stable Child-Pugh B7 * Written informed consent and willingness to comply with study follow-up and data collection Exclusion Criteria: * Prior systemic therapy for hepatocellular carcinoma, including immunotherapy, targeted therapy, or chemotherapy * Decompensated or clinically unstable liver disease, including refractory ascites, recurrent hepatic encephalopathy, active gastrointestinal bleeding, or - Child-Pugh class greater than B7 * Major bleeding risk or clinically significant coagulation abnormality, including recent gastrointestinal bleeding or untreated/high-risk gastroesophageal varices * Active autoimmune disease or long-term systemic immunosuppressive therapy * Active severe infection, including uncontrolled bacterial or fungal infection, uncontrolled hepatitis B virus replication without appropriate antiviral treatment, or active tuberculosis * Uncontrolled central nervous system metastases * Uncontrolled cardiovascular disease, including poorly controlled hypertension, recent myocardial infarction, unstable angina, stroke, or major thrombotic event * Significant proteinuria or renal dysfunction considered unsuitable for study treatment * Another active malignancy, except for selected low-risk malignancies allowed by the investigator and ethics committee * Pregnancy or breastfeeding * Known severe hypersensitivity to study-related drugs * Poor compliance, psychiatric or cognitive disorder preventing study participation, or any other condition judged by the investigator to make the participant unsuitable for the trial
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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
1 site. 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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Tongji Hospital, Tongji Medical College, Huazhong University of Science and Technology
Wuhan, Hubei, 430030, China
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Other studies related to the condition(s) this trial covers.
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