跳至主要内容
临床试验/NCT04053972
NCT04053972Unknown3 期

The Impact on Recurrence Risk of Adjuvant Lenvatinib for Patients With Hepatocellular Carcinoma And Microvascular Invasion (MVI) After 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 377 人开始时间: 2018年1月31日最近更新:
适应症
干预措施
相关药物

试验速览

阶段
3 期
发起方
入组人数
377
试验地点
1
主要终点
RFS

研究概览

简要总结

To compare The Impact on Recurrence Risk of Adjuvant Lenvatinib for Patients With Hepatocellular Carcinoma And Microvascular Invasion (MVI) After Hepatectomy.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
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<3; proven hepatocellular carcinoma with MVI according pathological examination; not previous treated for tumor; tumor was removed in operation; no recurrence occurence at 4 to 7 weeks after surgery; the lab test could meet: neutrophil count≥1.5×109/L; hemoglobin≥80g/L; platelet count≥60×109/L; serum albumin≥28g/L; total bilirubin<3-times upper limit of normal; ALT<5-times upper limit of normal; AST<5-times upper limit of normal; serum creatine<1.5-times upper limit of normal; PT≤upper limit of normal plus 6 seconds; INR≤2.3; sign up consent; unrolled by other clinical trials about hepatocellular carcinoma.

排除标准

  • cannot tolerate lenvatinib; CNS or bone 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 hemorreage or cardiac/brain vascular events within 30 days; pregnancy;

研究组 & 干预措施

treatment group

Experimental

adjuvant lenvatinib

干预措施: Lenvatinib (Drug)

结局指标

主要结局

RFS

时间窗: From date of randomization until the date of recurrence, assessed up to 60 months

recurrence-free survival

次要结局

  • recurrence rate(1 year, 2 year, 3 year, 5 year after surgery)
  • OS(From date of randomization until the date of death from any cause, 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)

Loading locations...

相似试验