The Efficacy of Sequential Treatment With Bevacizumab Combined With Atezolizumab in Advanced Liver Cancer With MASLD

Trial statusRecruiting
Trial phasePhase 2, Phase 3
Trial typeInterventional
Biological sexAll
Age18+
SponsorEastern Hepatobiliary Surgery Hospital

About this trial

This research plan involves a treatment approach for advanced hepatocellular carcinoma (HCC) in the context of metabolic-associated steatotic liver disease (MASLD). The study aims to compare the efficacy differences between sequential therapy and concurrent therapy using bevacizumab and atezolizumab for advanced HCC in MASLD. The research will focus on evaluating objective response rates, progression-free survival, disease control rates, and overall survival, while utilizing biomarker analysis to elucidate treatment mechanisms. Additionally, the study will examine treatment safety, including the incidence and severity of adverse events.

Eligibility criteria

Qualifiers

ECOG performance status of 0-1

Preoperative imaging diagnosis of advanced hepatocellular carcinoma (BCLC stage C or D, unsuitable for surgery)

Ultrasound or MRI indicating moderate to severe fatty liver (Fibroscan CAP > 268 dB/m or MR fat score > 10%)

Willing to use contraceptive measures during the trial period

Disqualifiers

Excessive alcohol consumption (weekly ethanol intake: males < 210 g, females < 140 g)

Tumor lesions previously treated with targeted therapy, immunotherapy, TACE, or radiotherapy

Pregnant or breastfeeding women, or positive pregnancy test at baseline

Central nervous system metastases diagnosed by CT, MRI, or PET-CT

Trial design

Treatments tested in this trial

  • Sequential treatment of bevacizumab combined with atezolizumab (sequential group)
  • Simultaneous treatment of bevacizumab combined with atezolizumab (same period group)

Treatment groups

20 Participants
are divided into 2 treatment groups