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Taking people in EgyptNo phase

Tests banding of esophageal varices in liver cancer patients receiving atezolizumab and bevacizumab

Tests band ligation of small varices in adults with liver cancer receiving atezolizumab and bevacizumab.

Plain-language title generated from the registry record
Registry title: Esophageal Varices Prophylaxis in Hepatocellular Carcinoma Treated With Atezolizumab and Bevacizumab

Key facts

Where
Tanta, EgyptSee the site

Where in Egypt

  • Tanta University HospitalsTanta, EgyptTaking people

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Trial details

Who runs it
Tanta University
Trial code
NCT06961526
Record updated
8 May 2025
Original description
The goal of this prospective cohort study is to evaluate the progression of esophagogastric varices in patients treated with atezolizumab-bevacizumab. Assess the efficacy of primary prophylaxis of small esophageal varices with no risky signs and shortening endoscopic follow-up time intervals to reduce the risk of variceal hemorrhage.Read full original descriptionShow less

Primary Prophylaxis of Esophageal Varices in Patients Treated With Atezolizumab and Bevacizumab for Advanced Hepatocellular Carcinoma.

The goal of this prospective cohort study is to evaluate the progression of esophagogastric varices in patients treated with atezolizumab-bevacizumab. Assess the efficacy of primary prophylaxis of small esophageal varices with no risky signs and shortening endoscopic follow-up time intervals to reduce the risk of variceal hemorrhage.

Researchers will assess the progression of esophageal varices (EVs) with no bleeding stigmata in patients treated with atezolizumab-bevacizumab therapy at 3, 6, 9, and 12 months with endoscopic examination. Evaluate the effect of shortening the endoscopic follow-up intervals to reduce the risk of variceal bleeding in patients treated with atezolizumab-bevacizumab therapy. Researchers will also assess the efficacy of variceal band ligation in small varices without bleeding stigmata before starting atezolizumab-bevacizumab therapy to reduce the progression of EVs.

Participants will undergo history-taking, clinical examination, laboratory investigations, Triphasic CT abdomen with contrast or MRI (for evaluation of tumor site, size and number), abdominal ultrasonography, and upper endoscopy (within 6 months before beginning of systemic therapy and followed up after 3, 6, 9, and 12 months).

Inclusion: Patients with confirmed advanced HCC (Diagnosed by two imaging modalities or liver biopsy) eligible for atezolizumab-bevacizumab therapy; Patients with preserved liver function (compensated Child-Pugh A if there is underlying cirrhosis); Patients with performance status ≤2 at staging work-up; Patients with no or grade 1 non-risky esophageal varices on pretreatment endoscopic examination.

Exclusion: Vascular disorders and arterial hypertension; Severe autoimmune disorders; Child-Pugh class C patients; Patients with performance status >2 at staging work-up; Patients who lost follow-up; Pregnant or breastfeeding women; Unwilling to participate in our study.

ClinicalTrials.gov NCT06961526