Massive liver cancer study aims to personalize treatment for 2000 patients
NCT ID NCT07156617
First seen Jun 26, 2026 · Last updated Jun 26, 2026
Summary
This study will analyze data from 2000 liver cancer patients to see how well interventional therapy combined with systemic drugs (like targeted therapy and immunotherapy) works in real life. Researchers will look at differences in outcomes and side effects, and use machine learning to predict risks. The goal is to help doctors tailor treatments to each patient.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- Interventional therapy (procedure) and systemic therapy (drugs like Lenvatinib, Apatinib, Camrelizumab, Tislelizumab)
- What this could lead to
- If successful, this could help doctors personalize liver cancer treatment by identifying which patients benefit most from combined therapy and predicting side effects.
- What could go wrong
- This is an observational study, not a controlled trial, so it cannot prove cause and effect. Results may vary across patients and may not apply to everyone.
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.
- Participants
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About 2,000 people
The number the study aims to enrol. It can still change while the study runs.
- Expected to start
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Oct 2025
An estimate. Start dates often move.
- Expected to finish
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Oct 2028
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.
Who is studied
Hepatocellular carcinoma
- 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.
Inclusion Criteria: * 1\. Age ≥ 18 years old, gender not restricted; 2. Diagnosed with HCC through pathological or imaging examination, and meeting the diagnostic criteria of the "Primary Liver Cancer Diagnosis and Treatment Guidelines (2024 Edition)"; 3. Has received or plans to receive interventional therapy combined with systemic treatment (including but not limited to DEB-TACE combined with targeted therapy, DEB-TACE combined with targeted therapy and immunotherapy, DEB-TACE combined with targeted therapy and immunotherapy other local interventional treatments (such as HAIC, ablation, particle implantation, etc.)); 4. Has completed baseline clinical information and treatment records, can cooperate with the follow-up arrangement, and has the willingness and ability to complete the entire research process; 5. Signed the informed consent form. Exclusion Criteria: * 1\. Diagnosed with liver metastatic cancer or other primary malignant tumors that are not HCC, or with concurrent other active primary malignant tumors; 2. Clearly have severe cognitive impairment, mental illness or confusion, and are unable to cooperate with the visit or fill out the scale; 3. Expected survival period is less than 3 months or clinical judgment indicates that follow-up cannot be completed; 4. Liver function is in decompensation, with Child-Pugh classification as C; 5. The investigator considers any other situation that is not suitable for participating in this study.
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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
14 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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Deng zhou People's Hospital
Dengzhou, Henan, China
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First People's Hospital of Shangqiu
Shangqiu, Henan, China
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Huai He Hospital of Henan University
Kaifeng, Henan, China
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Jiangxi Provincial People's Hospitail
Nanchang, Jiangxi, China
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Luo Yang Central Hospital
Luoyang, Henan, China
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Second People's Hospital of Jiaozuo
Jiaozuo, China
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The First Affiliated Hospital of Henan University of science and Technology
Luoyang, Henan, China
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The First Affiliated Hospital of Nanchang University
Nanchang, Jiangxi, China
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The First Affiliated Hospital of Zhengzhou University
Zhengzhou, Henan, China
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The Second Affiliated Hospital of Hainan Medical Universsity
Haikou, Hainan, China
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The Second People's Hospital of Jiaozuo
Jiaozuo, Henan, China
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Wuxi No.5 People's Hospital
Wuxi, Jiangsu, China
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Xingtai No.5 Hospital
Xingtai, Hebei, China
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Zhou Kou Central Hospital
Zhoukou, Henan, China
More trials for these conditions
Other studies related to the condition(s) this trial covers.
- Zapping liver tumors to make them operable
- Triple drug combo targets advanced liver cancer in new trial
- 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?