Clinical trial Recruiting at 1 site Observational Ages 18 and up

SIRT-Y90 with Atezolizumab and Bevacizumab for unresectable liver cancer

Official title: Efficacy and Safety of SIRT-Y90 in Combination With Atezo + Bev for Unresectable Hepatocellular Carcinoma

Run by Air Force Military Medical University, China · NCT07610551 · Data updated 2026-11-12

This study looks at whether adding SIRT-Y90 to atezolizumab and bevacizumab can help adults with unresectable hepatocellular carcinoma see better responses and keep cancer from progressing.

More HCC - Hepatocellular Carcinoma trials

Quick facts

Study typeObservational
Ages18 Years and up
SexAll
Enrollment50 (estimated)
SponsorAir Force Military Medical University, China
Academic / other
Drugs / interventionsatezolizumab, bevacizumab, radiation
Locations1 site (Xi’an, Shanxi)
StatusRecruiting
StartedFebruary 9, 2022
Main results expectedDecember 1, 2026
Study endsDecember 31, 2026
Registry record updatedMay 28, 2026
Trial IDNCT07610551 on ClinicalTrials.gov

Is this trial a fit for you?

Likely a good fit

Adults (≥18) with unresectable hepatocellular carcinoma who have received at least one cycle of atezolizumab plus bevacizumab and one cycle of SIRT-Y90, with at least one post-treatment visit.

Probably not a fit

Patients who do not respond to the triple therapy or who have competing health issues limiting benefit may not experience improvement.

A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.

What this trial studies

This is an observational bidirectional cohort study conducted across approximately eight sites in China. It combines retrospective data on prior treatments and outcomes with prospective follow-up to assess long-term recurrence, progression, and survival after starting SIRT-Y90 in combination with atezolizumab and bevacizumab. Primary endpoint is objective response rate using RECIST 1.1 and mRECIST, with secondary endpoints including progression-free survival, overall survival, and AFP reduction. Eligible patients are adults with unresectable HCC who have received at least one cycle of the triple therapy (or SIRT-Y90 alone in some cases) and have at least one post-treatment visit recorded. The analysis will describe efficacy and safety in this real-world setting in China.

Why it matters

Potential benefit: If successful, this approach could offer a new treatment option that may improve tumor responses and survival for patients with unresectable HCC.

How similar studies have gone: Previous studies in similar multidisciplinary approaches suggest potential benefits, but data in this exact combination and real-world setting are limited and exploratory.

Who can join: the full rules

Show full inclusion / exclusion criteria
Inclusion Criteria:

* Age ≥18 years old A diagnosis of unresectable HCC was made. HCC can be diagnosed clinically or pathologically.

At least one Atezo plus Bev administration and one cycle of SIRT-Y90 treatment. At least one visit was recorded after the initiation of Atezo + Bev and SIRT-Y90

Exclusion Criteria:

* Concomitant cancers other than BCC were diagnosed before or at the start of Atezo + Bev or SIRT-Y90 Participate in an interventional clinical study before or at the time of initiation of treatment with Atezo + Bev or SIRT-Y90

Where it's running

  • No. 777, Xitai Road, Chang'an District, Xi'an City, Shaanxi Province, China
    Xi’an, Shanxi, China
    Recruiting

Study contacts

Similar studies

Other studies for the same condition or treatment. Recruiting studies are listed first.

How to take part

  1. Review the eligibility criteria above with your treating physician.
  2. Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
  3. Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.
Last reviewed 2026-11-14 by the Find a Trial editorial team. Information on this page is for educational purposes and is not medical advice. Always consult qualified healthcare professionals about clinical trial participation.