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临床试验/NCT03851887
NCT03851887Unknown2 期

The Efficacy of Transarterial Chemoinfusion (TAI) Combine Stereotactic Body Radiation Therapy (SBRT) in Unresectable Hepatocellular Carcinoma (HCC): A Prospective, Single-armed, Stage II Clinical Trial

Sun Yat-sen University1 个研究点 分布在 1 个国家目标入组 33 人开始时间: 2018年12月1日最近更新:
适应症
干预措施

试验速览

阶段
2 期
发起方
入组人数
33
试验地点
1
主要终点
PFS

研究概览

简要总结

To evaluate the efiicacy of TAI combine SBRT in unresectable HCC

研究设计

研究类型
Interventional
分配方式
Na
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 advanced hepatocellular carcinoma according patological examination or EASL/AASLD diagnostic criteria;
  • not previous treated for tumor;
  • cannot accepted hepatectomy;
  • 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 SBRT;
  • 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.

研究组 & 干预措施

treatment group

Experimental

TAI combine SBRT

干预措施: TAI combine SBRT (Combination Product)

结局指标

主要结局

PFS

时间窗: From date of randomization until the date of progression, assessed up to 36 months

progression-free survival

ORR

时间窗: From date of randomization until the date of death, assessed up to 36 months

objective response rate

次要结局

  • OS(From date of randomization until the date of death from any cause, assessed up to 36 months)
  • DCR(From date of randomization until the date of death, assessed up to 36 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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