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临床试验/NCT06024252
NCT06024252尚未招募不适用

Efficacy, Safety, and Treatment Patterns of Transcatheter Arterial Chemoembolization (TACE) Combined With Atezolizumab and Bevacizumab in Unresectable Hepatocellular Carcinoma: a Multicenter, Retrospective, Observational Real-world Study

Zhongda Hospital0 个研究点目标入组 200 人开始时间: 2023年9月1日最近更新:
适应症
相关药物

试验速览

阶段
不适用
状态
尚未招募
发起方
入组人数
200
主要终点
Overall survival

研究概览

简要总结

This study will evaluate the efficacy and safety of TACE combined with atezolizumab + bevacizumab in the treatment of unresectable hepatocellular carcinoma, and the treatment patterns of the combination regimen

详细描述

This study is a multi-center, retrospective and observational real-world study to explore the efficacy, safety and treatment pattern of TACE combined with Atezolizumab + Bevacizumab in unresectable hepatocellular carcinoma. The target population for the planned retrospective analysis of this project is patients who have been diagnosed with unresectable HCC according to the guidelines for Diagnosis and Treatment of Primary Liver Cancer in China (2019 Edition) and treated with TACE combined with atezolizumab + bevacizumab.

研究设计

研究类型
Observational
观察模型
Cohort
时间视角
Retrospective

入排标准

年龄范围
18 Years 至 —(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • All patients were diagnosed with unresectable hepatocellular carcinoma according to the guidelines for Diagnosis and Treatment of Primary Liver Cancer in China (2019 Edition);
  • Patients ≥ 18 years old, male or female;
  • Child-Pugh Class A and B liver function;
  • ECOG-PS score of 0 ~ 2 points;
  • Received TACE in combination with atezolizumab + bevacizumab for at least one interval of no more than eight weeks.

排除标准

  • Other primary malignancies;
  • Incomplete data, such as no baseline image that can be assessed according to RECIST 1.1 or mRECIST, and survival outcome.

结局指标

主要结局

Overall survival

时间窗: 1 year

Overall survival (OS): defined as the time from the start of the first TACE or atezolizumab + bevacizumab (whichever occurs first) to death due to any cause.

次要结局

  • Objective response rate(1 year)
  • Immune-TACE PFS(1 year)
  • Progression-Free Survival(1 year)
  • Disease control rate(1 year)
  • Treatment pattern(1 year)
  • One-year survival rate(1 year)

研究者

发起方
Zhongda Hospital
申办方类型
Other
责任方
Principal Investigator
主要研究者

Gao-jun Teng

Dr. Gao-Jun Teng

Zhongda Hospital

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