Radiation plus immunotherapy may make inoperable liver cancer operable
NCT ID NCT07305428
First seen Jun 26, 2026 · Last updated Jun 27, 2026 · Updated 1 time
Summary
This pilot study is testing whether combining stereotactic body radiation therapy (SBRT) with immunotherapy can shrink liver tumors that are too large or widespread to be surgically removed. The goal is to make these tumors operable, giving patients a chance at curative surgery. The study will enroll 30 adults with unresectable hepatocellular carcinoma (HCC) and will measure how many patients are successfully downstaged to become surgical candidates.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- Stereotactic body radiation therapy (SBRT) followed by immunotherapy drugs
- What this could lead to
- If successful, this approach could allow some patients with inoperable liver cancer to become candidates for surgery, potentially improving their long-term survival.
- What could go wrong
- This is a very early pilot study with only 30 participants. It is not yet known if the combination will be effective or safe, and immunotherapy can cause serious side effects.
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
-
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
-
About 30 people
The number the study aims to enrol. It can still change while the study runs.
- Started
-
Apr 2019
- Expected to finish
-
Dec 2030
An estimate. End dates often move.
- Lead sponsor
-
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
-
18 to 80 years
- Sex
-
Anyone
- Healthy volunteers
-
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: * Diagnosis of HCC is made according to American Association for the Study of Liver Diseases (AASLD) practice guideline 2010: patients with cirrhosis of any etiology and patients with chronic hepatitis B (HBV) who may not have fully developed cirrhosis, the presence of liver nodule \>1cm and demonstrated in a single contrast enhanced dynamic imaging \[either computed tomography (CT) or magnetic resonance imaging (MRI)\] of intense arterial uptake and "washout" in portal venous and delayed phases. * Tumor size 5-25 cm or number of lesions ≤3 or segmental portal vein involvement * Age: 18-80 years old * Child Pugh liver function class A-B7 * Eastern Cooperative Oncology Group (ECOG) performance status score of 0 or 1 Exclusion Criteria: * Prior invasive malignancy * Prior radiotherapy to the region of liver or selective internal radiotherapy * Severe, active co-morbidity * Presence of extra-hepatic metastases (M1) * Main portal vein or inferior vena cava (IVC) thrombosis or involvement * Presence of ascites or encephalopathy * Contraindicated of SBRT: * Any one hepatocellular carcinoma \> 15 cm * Total maximal sum of hepatocellular carcinoma \> 25 cm * More than 3 discrete hepatic nodule * Direct tumor extension into the stomach, duodenum, small bowel, large bowel, common or main branch of biliary tree
Get updates
Get notified about this study
Sign up to get updates when this study changes or when new studies for HCC - hepatocellular carcinoma are added.
Genom att skicka in godkänner du våra Användarvillkor
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.
-
The study's own enquiry address
This study publishes an address for enquiries. See it below .
-
The places running it
1 site. The list below names each one and where it is.
-
The official record
ClinicalTrials.gov lists the study team's own contact details, including names and phone numbers. We don't republish those.
-
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
Show contact details
Enter your email to view the contact information for this study.
Genom att skicka in godkänner du våra Användarvillkor
Study contacts
-
Contact
Email: •••••@•••••
Locations
-
Queen Mary Hospital
RECRUITINGHong Kong, Hong Kong
Contact Email: •••••@•••••
More trials for these conditions
Other studies related to the condition(s) this trial covers.
- Can scans predict which liver cancer patients need extra local therapy?
- Can a website help liver cancer patients care for themselves during chemoembolization?
- Can removing the spleen help the liver fight cancer?
- Liver cancer treatments under Real-World scrutiny
- Can a Three-Pronged attack shrink untreatable liver tumors?
- Can protein patterns in stored tumors point to new treatment targets?