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临床试验/NCT03851913
NCT03851913招募中3 期

The Impact on Survival of Neo-adjuvant Transarterial Chemoinfusion (TAI) for Patients With Beyond Milan Criteria BCLC Stage A/B Hepatocellular Carcinoma Who Underwent Hepatectomy: A Random, Controlled, Stage III Clinical Trial

Sun Yat-sen University1 个研究点 分布在 1 个国家目标入组 344 人开始时间: 2018年7月1日最近更新:
适应症

试验速览

阶段
3 期
状态
招募中
发起方
入组人数
344
试验地点
1
主要终点
OS

研究概览

简要总结

To compare the impact on survival of neo-adjuvant TAI for patients with beyond Milan criteria BCLC stage A/B HCC who underwent hepatectomy.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Single Group
主要目的
Treatment
盲法
None

入排标准

年龄范围
18 Years 至 75 Years(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • older than 18 years old and younger than 75 years;
  • ECOG PS≤1;
  • proven hepatocellular carcinoma according patological examination or EASL/AASLD diagnostic criteria;
  • not previous treated for tumor;
  • the tumor was diagnosed as BCLC stage A/B and beyond Milan criteria;
  • no distant metastasis;
  • the lab test could meet:
  • neutrophil count≥2.0×109/L;
  • hemoglobin≥100g/L;
  • platelet count≥75×109/L;
  • serum albumin≥35g/L;
  • total bilirubin<2-times upper limit of normal;
  • ALT<3-times upper limit of normal;
  • AST<3-times upper limit of normal;
  • serum creatine<1.5-times upper limit of normal;
  • PT≤upper limit of normal plus 4 seconds;
  • sign up consent.

排除标准

  • cannot tolerate TAI or surgery;
  • distant metastasis exits;
  • known history of other malignancy;
  • be allergic to related drugs;
  • underwent organ transplantation before;
  • be treated before (interferon included);
  • known history of HIV infection;
  • known history of drug or alcohol abuse;
  • have GI hemorrhage or cardiac/brain vascular events within 30 days;
  • pregnancy.

结局指标

主要结局

OS

时间窗: From date of randomization until the date of death from any cause, assessed up to 60 months

overall survival

次要结局

  • RFS(From date of randomization until the date of recurrence, assessed up to 60 months)
  • recurrence rate(1 year, 2 year, 3 year, 5 year after surgery)
  • PFS(From date of randomization until the date of progression, assessed up to 60 months)

研究者

发起方
Sun Yat-sen University
申办方类型
Other
责任方
Principal Investigator
主要研究者

Rong-ping Guo

Professor

Sun Yat-sen University

研究点 (1)

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