Radiation boost may extend life for liver cancer patients after immunotherapy stalls
NCT ID NCT06434480
First seen Jun 27, 2026 · Last updated Jun 27, 2026
Summary
This study looks at whether adding focused radiation to spots where cancer is growing can help people with advanced liver cancer whose first immunotherapy treatment has partly stopped working. About 30 adults with limited new growth will receive radiation to those spots while continuing their current therapy. The goal is to see if this approach can delay further cancer spread and improve survival.
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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 30 people
The number the study aims to enrol. It can still change while the study runs.
- Started
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Jun 2024
- Expected to finish
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Mar 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.
- 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. Patients aged ≥ 18 years old 2. ECOG performance 0 to 1 3. Confirmed diagnosis of HCC 4. Oligoprogression on first-line immunotherapy, as defined as ≤ 5 lesions (intra- and extrahepatic lesions all together; vascular tumor thrombus is counted as one lesion) * First-line immunotherapy that are allowed in this study include atezolizumab plus bevacizumab, durvalumab plus tremelimumab, durvalumab, nivolumab and ipilimumab, which are approved by the FDA and have been used in Hong Kong. 5. Progressed lesion(s) amenable to SBRT: * For intrahepatic progression: * Number of intrahepatic progression ≤ 5 * Total intrahepatic tumours ≤ 10 * Maximum sum of HCC ≤ 20cm * Any one HCC ≤ 20cm * Normal liver volume minus intrahepatic GTV \> 700cc * Mean liver dose ≤ 15Gy * No measurable common or main branch biliary duct involvement * No direct tumor invasion into the stomach, duodenum, small bowel or large bowel * For extrahepatic progression: * Maximal tumor size ≤ 7cm * Respective dose constraints of organ at risks as listed on the UK 2022 Consensus on Normal Tissue Dose-Volume Constraints for Oligometastatic, Primary Lung and Hepatocellular Carcinoma Stereotactic Ablative Radiotherapy can be met and ASTRO guideline. 6. Prior radiofrequency ablation (RFA) or trans-arterial chemoembolization (TACE) are eligible 7. Child-Pugh A liver function 8. Life expectancy longer than 12 weeks 9. At least one measurable treatment lesion according to RECIST 1.1 10. Written informed consent must be obtained prior to any study related procedures 11. Adequate haematological function (Hb ≥ 8.5g/dL; Plt ≥ 50x10\^9/L; ANC ≥ 1.0x10\^9/L; INR ≤ 1.5) 12. Adequate hepatic function (albumin ≥ 28g/L; Bilirubin ≤ 2.5xULN; ALT \< 5 times upper limit normal) 13. Adequate renal function (serum creatinine ≤ 1.5 times the upper limit of normal range; Na ≥ 130mmol/L; K ≥ 3.0mmol/L) 14. Able to read, understand and provide written consent Exclusion Criteria: 1. History of another malignancy except appropriately-treated BCC of skin or CIN of cervix during the last 5 years 2. Previous radiotherapy to the abdomen 3. Previous yttrium-90 chemoembolization 4. Repetitive history of non-healing wounds or ulcers within 2 months of inclusion 5. Pregnant or lactating females at any time during the study 6. Active autoimmune disease requiring systemic therapy in the past 2 years 7. Diagnosis of immunodeficiency (including HIV) 8. Ongoing corticosteroid therapy \>10mg prednisone daily
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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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Department of Clinical Oncology, Prince of Wales Hospital
RECRUITINGHong Kong, Hong Kong
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Other studies related to the condition(s) this trial covers.
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- Simple blood test aims to catch liver cancer before It's too late
- Engineered virus takes on liver cancer when standard treatment fails
- Ultrasound vs. MRI: which spots hidden liver cancer better?
- Epigenetic drug may re-sensitize liver tumors to immunotherapy