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临床试验/NCT03275376
NCT03275376终止2 期

Statin Combination Therapy in Patients Receiving Sorafenib for Advanced Hepatocellular Carcinoma: A Randomized Controlled Study

Taichung Veterans General Hospital1 个研究点 分布在 1 个国家目标入组 34 人开始时间: 2017年12月21日最近更新:
适应症
干预措施
相关药物

试验速览

阶段
2 期
状态
终止
入组人数
34
试验地点
1
主要终点
Overall survival

研究概览

简要总结

Target therapy with sorafenib is the standard of treatment for advanced Hepatocellular carcinoma (HCC), but the patient survival time is still unsatisfactory. The aims of this study are to prove statins improve the tumor responses and overall survival for patients who receive sorafenib therapy for advanced HCC by a prospective randomized controlled study.

详细描述

Background:

Hepatocellular carcinoma (HCC) is the second leading cause of cancer death worldwide, including the condition in Taiwan, and the management of HCC is an important challenge in public health. Target therapy with sorafenib is the standard of treatment for advanced HCC (vascular invasion or extrahepatic metastasis), but the patient survival time is still unsatisfactory. In recent years, growing evidences, including mechanism analysis, have suggested the anitneoplastic effects of statin, and a recent pooled analysis found that statin use may be associated with improved survival in patients with metastatic rencal cell carcinoma. However, a prospective clinical trial of statin sorafenib combination therapy in the treatment of advanced HCC is lacking.

Aims:

  1. To prove statins improve the overall survival for patients who receive sorafenib therapy for advanced HCC by a prospective randomized controlled study.
  2. To prove statin can improve tumor responses and the progression free survival for patients who receive sorafenib therapy for advanced HCC by a prospective randomized controlled study.

Methods:

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
Quadruple (Participant, Care Provider, Investigator, Outcomes Assessor)

入排标准

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

入选标准

  • Patients more than 40 years old
  • HCCs diagnosed by AASLD image criteria or pathology
  • HCCs in BCLC advanced stage, with portal vein thrombosis (VP3 or VP4) or extrahepatic metastasis
  • Not suitable or failed to locoreginal treatments for HCC
  • Child-Pugh score = or < 6
  • ECOG performance status (PST) 0-2
  • Serum bilirubin < 2 mg/dL and prothrombin time (PT) prolongation < 3 seconds
  • Will receive sorafenib therapy
  • Life expectancy > 3 months
  • Will follow the pregnancy prevention protocol

排除标准

  • HCC is considered for curative therapy
  • HCC with brain metastasis
  • History of systemic therapy for HCC
  • Indications for statin use, such as hyperlipidemia in cardiovascular diseases
  • Any local treatment for HCC within 4 weeks
  • Any active gastrointestinal bleeding within 4 weeks
  • Liver transplant history or concomitant immunosuppressive therapy
  • Concurrent any other malignancy
  • Allergy to sorafenib or statins
  • Pregnancy or lactation
  • Serum AST or ALT > 5x upper limit of normal
  • Known HIV infection
  • eGFR < 30 ml/min
  • Abnormal medical conditions that are unsuitable for study, such as uncontrolled hypertension, coronary arterial disease, or arrhythmia

研究组 & 干预措施

Statin treated group

Experimental

干预措施: Atorvastatin 10mg (Drug)

Control group

Placebo Comparator

干预措施: Placebo Oral Tablet (Drug)

结局指标

主要结局

Overall survival

时间窗: Three year

次要结局

  • Best tumor response(Three year)
  • Progression free survival(Three year)

研究者

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

Teng-Yu Lee

MD, PhD

Taichung Veterans General Hospital

研究点 (1)

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