跳至主要内容
临床试验/NCT01860222
NCT01860222Unknown不适用

A Prospective Randomized Trial of Surgical Resection Versus Percutaneous Local Ablative Therapy for Hepatocellular Carcinoma Complicating Clinically Significant Portal Hypertension Within the Milan Criteria

Eastern Hepatobiliary Surgery Hospital1 个研究点 分布在 1 个国家目标入组 160 人开始时间: 2011年1月最近更新:
适应症

试验速览

阶段
不适用
入组人数
160
试验地点
1
主要终点
overall survival

研究概览

简要总结

The aim of this study is to compare the operative complication and short-/long-term therapeutic effects of percutaneous local ablative therapy (PLAT) versus surgical resection(SR) on small hepatocellular carcinoma(HCC) patients with clinically significant portal hypertension(CSPH) so as to lend clinical and theoretical basis of the therapeutic schemes for the disease.

详细描述

HCC is a major health problem worldwide, with an estimated incidence ranging between 500,000 and 1,000,000 new cases annually. It is the fifth most common cancer in the world and the third most common cause of cancer-related death,especially in East-Asia countries.SR remains the first therapeutic option for a cure but is suitable only for 9%-27% of patients.The presence of significant background cirrhosis often precludes liver resection for HCC.Even though these HCC patients undergo SR,the incidence of posthepatectomy liver failure(PHLF) and death would be high,especially to HCC patients complicating CSPH,whose corresponding risk of PHLF and persistent PHLF were 59.02%and 14.75%respectively in our past study. It is extremely urgent to search a safe and effective means in this subgroup of HCC patients.PLAT, a recently developed local ablative technique, has attracted the greatest interest and popularity because of its effectiveness and safety,with a 3-year survival rate of 62-77%,a low treatment complication rate of 8-9% and a low treatment mortality rate of 0-0.5%.However, there is still debate on whether PLAT or SR is the most suitable therapy for HCC.To our knowledge,there have been no study on the therapy of HCC complicating CSPH.

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 70 Years(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • 18 Years < ge ≤ 70 Y,KPS ≥ 70
  • A solitary HCC ≤ 5cm in diameter,or multiple HCC(≤3) ,each ≤3cm in diameter without evidence of radiologically definable vascular invasion or extrahepatic metastasis. allowing to both SR and PLAT
  • Child-Pugh class A or B,without history of encephalopathy,ascites refractory to diuretics,or variceal bleeding
  • NO previous treatment of HCC
  • Platelet count>40,000/mm3;prothrombin time prolongation of no more than 3 seconds
  • Patients who can understand this trial and have signed information consent

排除标准

  • metastatic liver cancer
  • Patients with apparent cardiac,pulmonary,cerebral and renal dysfunction,which may affect the treatment of HCC
  • Patients with other diseases which may affect the treatment mentioned
  • 4) Patients participating in other clinical trials
  • 5) Patients with a medical history of other malignant tumors
  • Pregnant and breast-feeding women

结局指标

主要结局

overall survival

时间窗: 3 years

次要结局

  • local tumor progression(3 years)

研究者

申办方类型
Other
责任方
Principal Investigator
主要研究者

ShenFeng

vice president of the Eastern Hepatobiliary Surgery Hospital

Eastern Hepatobiliary Surgery Hospital

研究点 (1)

Loading locations...

相似试验