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临床试验/NCT02138981
NCT02138981Unknown4 期

Hepatic Resection Versus Transarterial Chemoembolization as the Initial Treatment for Resectable Hepatocellular Carcinoma Beyond Milan Criteria

Sun Yat-sen University1 个研究点 分布在 1 个国家目标入组 436 人开始时间: 2014年5月1日最近更新:
适应症
干预措施

试验速览

阶段
4 期
发起方
入组人数
436
试验地点
1
主要终点
overall survival time

研究概览

简要总结

The purpose of this study is to compare the survival outcomes between hepatic resection and transarterial lipiodol chemoembolization (TACE) used as the initial treatment in patients with Resectable Hepatocellular Carcinoma Beyond Milan Criteria.

详细描述

For patients with large/multiple, and resectable hepatocellular carcinomas (HCCs) without macrovascular invasion or extrahepatic spread, the choice of treatment remains largely controversial. For these patients, transarterial lipiodol chemoembolization (TACE) is recommended as a palliative therapy.

On the other hand, many authors still believe that hepatic resection is the only potential curative treatment in these patients because it is still feasible to remove all macroscopic tumors safely at surgery. With advances in surgical techniques, more large/multiple HCCs are now resectable, and long-term results have been reported that ranged from 30% to 58% at 5 years; even patients with large bilobar multiple HCC could reach a survival rate of more than 20% at 5 years after hepatic resection.

Until now, there have been only a few studies that compared the outcomes of hepatic resection and TACE in the treatment of multiple HCCs, and these have reported controversial results. Some studies showed that hepatic resection had survival benefi t over TACE, but other studies showed the opposite result ( 11-15 ). Therefore, the investigators performed this prospective study in consecutive patients with large/multiple, and resectable HCCs to compare the outcomes in patients who underwent hepatic resection or TACE as the initial treatment.

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

  • A diagnosis of HCC based on the diagnostic criteria for HCC used by the European Association for the Study of the Liver (EASL).
  • The patient has not been previously treated with surgery, radiation therapy, radiofrequency ablation, percutaneous ethanol or acetic acid injection, or cryoablation.
  • The tumor beyound milan criteria.
  • The tumor was evaluated to be resectable by a same group of surgeon.
  • Patients must have at least one tumor lesion that can be accurately measured according to EASL criteria
  • No serious concurrent medical illness
  • Not pregnant or breast-feeding patients
  • Cirrhotic status of Child-Pugh class A only
  • The following laboratory parameters:
  • Platelet count ≥ 80,000/µL
  • Hemoglobin ≥ 8.5 g/dL
  • Total bilirubin ≤ 1.5 mg/dL Serum albumin ≥ 35 g/L
  • ASL and AST ≤ 5 x upper limit of normal
  • Serum creatinine ≤ 1.5 x upper limit of normal
  • INR ≤ 1.5 or PT/APTT within normal limits
  • Absolute neutrophil count (ANC) >1,500/mm3
  • Ability to understand the protocol and to agree to and sign a written informed consent document

排除标准

  • Tumor vascular invasion or distant metastases
  • Significant renal impairment (creatinine clearance < 30 mL/minute) or patients on dialysis
  • On anticoagulation or suffering from a known bleeding disorder
  • Unstable coronary artery disease or recent MI
  • Known history of HIV
  • History of organ allograft
  • Known or suspected allergy to the investigational agents or any agent given in association with this trial.
  • Cardiac ventricular arrhythmias requiring anti-arrhythmic therapy
  • Patients with clinically significant gastrointestinal bleeding within 30 days prior to study entry.
  • Any other hemorrhage/bleeding event > CTCAE Grade 3 within 4 weeks of first dose of study drug
  • Serious non-healing wound, ulcer, or bone fracture
  • Known central nervous system tumors including metastatic brain disease
  • severe Arterioportal Shunts or Arteriavein Shunts

研究组 & 干预措施

Chemoembolization and Response-Dependent Resection

Experimental

patients underwent transarterial chemoembolization (TACE) as initial treatments, and only patients who showed good response were subjected to surgical resection.

干预措施: Chemoembolization and Response-Dependent Resection (Procedure)

Immediate Resection

Active Comparator

patients received immediate surgical hepatic resection

干预措施: Immediate Resection (Procedure)

结局指标

主要结局

overall survival time

时间窗: 5 years

次要结局

  • disease free survival(5 years)
  • Number of Adverse Events(30 days)

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

Shi Ming

Professor

Sun Yat-sen University

研究点 (1)

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