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OncoMatch/Clinical Trials/NCT07239245

Study to Evaluate the Efficacy and Safety of Neo-Adjuvant TACE and Atezolizumab Plus Bevacizumab Therapy for High-Risk Recurrent Hepatocellular Carcinamo

Is NCT07239245 recruiting? Yes, currently enrolling (May 2026). This Phase 2 trial studies multiple treatments including Atezolizumab and Bevacizumab for resectable hepatocellular carcinoma with high risk of recurrence.

Phase 2RecruitingCancer Institute and Hospital, Chinese Academy of Medical SciencesNCT07239245Data as of May 2026

Treatment: Atezolizumab · BevacizumabThis is an open-label, single-arm, multicenter, prospective, phase II clinical study to evaluate the efficacy and safety of TACE combined with Atezolizumab and Bevacizumab as neoadjuvant treatment in Hepatocellular Carcinoma.

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Extracted eligibility criteria

Cancer type

Hepatocellular Carcinoma

Disease stage

Grade: Grade 3Grade 4

Initially resectable with high-risk recurrence factors. High-risk features for resected patients include tumor size >5 cm, tumor number >3, vascular invasion (microvascular invasion or macrovascular invasion - Vp1/Vp2 - of the portal vein) and poor tumor differentiation (defined as Grade 3 or 4).

Performance status

ECOG 0–1(Restricted strenuous activity)

Prior therapy

No prior treatment (treatment-naive required)
Max 0 prior lines

Cannot have received: locoregional or systemic treatment

No prior locoregional or systemic treatment for HCC

Cannot have received: investigational therapy

Treatment with investigational therapy within 28 days prior to initiation of study treatment

Lab requirements

Liver function

child-pugh a

Structured fields extracted by AI. May contain errors — verify against the official protocol.

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