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Study identifier: NCT07293468 Synced from ClinicalTrials.gov · July 29, 2026
● Recruiting

Comparison of SBRT and SIRT With Combination IO for Locally-advanced, Unresectable HCCs (BIIRTH)

Condition: Hepatocellular Carcinoma (HCC)  ·  Sponsor: Tuen Mun Hospital

PhasePhase 2/Phase 3
Planned participants106
Who can joinAll sexes, 18 Years to 80 Years
Healthy volunteersNo

About this study

The goal of this clinical trial is to compare the safety and efficacy of sequential Transarterial Chemoembolization (TACE) and Stereotactic body radiation therapy (SBRT) versus Y90-radioembolisation (SIRT), followed by systemic therapy in patients with large, locally advanced, unresectable Hepatocellular carcinoma (HCC). The main question it aims to answer is whether Sequential TACE-SBRT potentially gives longer Progression-free survival (PFS) benefit with similar toxicities as compared with Y90 SIRT. Participants will be recruited via multidisciplinary meetings (MDTs) with hepatobiliary surgeons, medical hepatologists and radiologists with consistent, strict considerations on eligibility and treatment alternatives. Eligible patients will be randomized in 1:1 ratio to received one of the two treatment arms.

This description comes directly from the study's public registry record.

Talk to the study team

Sean Man Natalie WONG  ·  852-24685088  ·  wsm011@ha.org.hk

Man TONG  ·  852-24685086  ·  tm326@ha.org.hk

Always discuss trial participation with your own doctor first.

Locations (1)

Tuen Mun HospitalHong Kong, Hong KongRecruiting

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Source record: clinicaltrials.gov/study/NCT07293468