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Radiation boost may extend life for liver cancer patients after immunotherapy stalls

NCT ID NCT06434480

What the study statuses mean

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Recruitment status, easiest to join first

Recruiting now This study
This trial is taking on new participants right now.
Not yet recruiting
Registered, but not yet taking participants.
By invitation only
Not open to general applications. Only people the study team invites can take part.
Paused
Paused for now. It may or may not start again.
Ongoing
Running, but no longer taking on new participants.
Completed
The trial has finished. Results may not be published yet.
Stopped early
Stopped early, before it reached the end. That can be for many reasons, including safety.
Cancelled
Cancelled before anyone took part.

Expanded access (not trials)

Expanded access
Not a trial. This treatment can be requested outside a study, case by case, for people who qualify.
Expanded access (paused)
Not a trial. The treatment can normally be requested outside a study, but is unavailable right now.
Expanded access (ended)
Not a trial. The treatment could once be requested outside a study, but no longer can.
Approved
The treatment has been approved, so it is available normally rather than through this programme.

When the status isn't known

Details not published
The full record has not been published yet, so there is little to show here.
Status unknown
This status has not been confirmed recently, so it may be out of date.

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.

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

Jun 2024

Expected to finish

Mar 2028

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 years and older

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

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.

  1. The places running it

    1 site. The list below names each one and where it is.

  2. The official record

    ClinicalTrials.gov lists the study team's own contact details, including names and phone numbers. We don't republish those.

    Open the record ↗

  3. 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

  • Department of Clinical Oncology, Prince of Wales Hospital

    RECRUITING

    Hong Kong, Hong Kong

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Other studies related to the condition(s) this trial covers.