RecruitingPhase 2NCT06819566

Prophylactic Endoscopic Variceal Ligation in Patients With High-risk Esophageal Varices Receiving Atezo/Bev for HCC

Prophylactic Endoscopic Variceal Ligation in Patients With High-risk Esophageal Varices Receiving Atezolizumab Plus Bevacizumab for Hepatocellular Carcinoma : A Phase II, Multicenter, Single-arm Trial (ESCOAT Trial)


Sponsor

Asan Medical Center

Enrollment

44 participants

Start Date

May 28, 2025

Study Type

INTERVENTIONAL

Conditions

Summary

The goal of this study is to evaluate whether prophylactic endoscopic variceal ligation (EVL) can prevent esophageal variceal bleeding in patients with hepatocellular carcinoma (HCC) receiving atezolizumab and bevacizumab (Atezo/Bev) therapy. The study will also assess the safety of prophylactic EVL in this population. The main question it aims to answer is: Does prophylactic EVL in high-risk varices reduce the incidence of variceal bleeding to a level similar to that of low-risk varices in HCC patients receiving Atezo/Bev? Participants will: 1. Undergo prophylactic EVL before starting Atezo/Bev therapy (within 2 weeks ± 1 week before the first dose). 2. Start Atezo/Bev therapy 2 weeks (± 1 week) after EVL. 3. Have follow-up endoscopies (EGD) one week after the 3rd, 5th, and 7th doses of Atezo/Bev. If varices improve, no additional intervention is needed. If varices persist or worsen, on-demand EVL will be performed, and Atezo/Bev will continue. This study will help determine if prophylactic EVL should be a standard strategy for managing high-risk varices in HCC patients undergoing Atezo/Bev therapy.


Eligibility

Min Age: 19 YearsMax Age: 80 Years

Plain Language Summary

Simplified for easier understanding

This study tests whether performing a preventive procedure to band enlarged veins in the esophagus (variceal ligation) before starting a standard liver cancer immunotherapy combination (atezolizumab + bevacizumab) reduces the risk of dangerous bleeding in patients with advanced liver cancer and high-risk varices. **You may be eligible if...** - You are between 19 and 79 years old - You have advanced liver cancer (hepatocellular carcinoma, BCLC stage C) with no prior systemic treatment - Your liver function is classified as Child-Pugh Class A (well-compensated) - You have high-risk esophageal varices on a recent endoscopy - Your blood counts and liver function meet required levels **You may NOT be eligible if...** - You have previously received systemic therapy for liver cancer - You have severe liver dysfunction (Child-Pugh B or C) - You are pregnant or breastfeeding - You have serious other organ problems Talk to your doctor to see if this trial is right for you.

This summary was AI-generated to explain the trial in plain language. It is not medical advice. Always discuss eligibility with your doctor before enrolling in a clinical trial.

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Interventions

PROCEDUREEndoscopic variceal ligation (EVL)

1. EVL for high-risk varices will be performed by experienced endoscopists, certified in gastroenterological endoscopy, within two weeks prior to the initiation of the Atezo/Bev. 2. A follow-up EGD will be conducted one week after the Atezo/Bev #3. If any of the following criteria are met, additional EVL will not be performed, and anticancer treatment will proceed two weeks later. Otherwise, an additional on-demand EVL session will be conducted: * The esophageal varices have improved to F1 or less. * The red color sign has disappeared. 3. On-demand EVL will be considered after 5th, and 7th consecutive doses of Atezo/Bev, with EGD follow-up performed to assess eligibility. The maximum number of EVL sessions is limited to three sessions.


Locations(1)

Liver cancer center, Asan Medical Center

Seoul, Song-pa, South Korea

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NCT06819566


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