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临床试验/NCT01018381
NCT01018381已完成不适用

Randomized Clinical Study of Arabinoxylan Rice Bran (MGN-3/Biobran) for the Treatment of Hepatocellular Carcinoma and Hepatitis B and C Infection

The 108 Military Central Hospital1 个研究点 分布在 1 个国家目标入组 130 人开始时间: 2006年6月最近更新:
适应症
干预措施
相关药物

试验速览

阶段
不适用
状态
已完成
发起方
入组人数
130
试验地点
1
主要终点
Patient survival

研究概览

简要总结

Hepatocellular carcinoma (HCC) is the sixth most common cancer worldwide with an estimated 626,000 new cases per year worldwide, accounting for 5.7% of new cancer cases. Although resection and transplantation offer the best 5-year survival rates, not all patients are suitable surgery candidates. Other treatments include pericutaneous ethanol injection (PEI), radiofrequency ablation (RFA), and transarterial oily chemoembolization (TOCE), all of which enhance the survival rate and aid in shrinkage of the tumor. The very low survival rate among HCC patients, 3-5%, reflects the inadequacy of conventional therapies for the disease and highlights the necessity of finding new treatments or modifying the current treatment.

The hepatitis B virus (HBV) causes liver disease that can range in severity from a mild illness that lasts several weeks (acute hepatitis B) to a long-term chronic illness. An estimated 2 billion people have been infected with HBV worldwide, resulting in more than 350 million individuals with chronic, long-term liver infections. Patients with chronic HBV infection are at a great risk for the development of cirrhosis, hepatic failure, and HCC. There is no cure for hepatitis B and care is mostly palliative. There are several anti-viral and interferon drugs, such as Entecavir and Interferon α therapy, which can help some patients. However, these drugs are costly, thousands of dollars per year, and are not widely available in many countries, especially in the developing world. Vaccination is available and effective and is recommended for all individuals at risk for HBV infection. However, vaccination is only effective in individuals who have not been exposed to HBV. Hepatitis B is closely linked to liver cancer, which is almost always fatal.

MGN-3/Biobran is an arabinoxylan extracted from rice bran that is treated enzymatically with an extract from Shiitake mushrooms. MGN-3 demonstrated anti-cancer activity in vivo in mice and humans. The present study was carried out to examine whether combining the current conventional treatment with a food supplement, arabinoxylan rice bran (MGN-3/Biobran), may improve the outcome of the disease and increase the survival rate of patients with HCC or HBV. We hypothesize that a combinatory treatment of conventional therapy with MGN-3/Biobran will augment the therapeutic effect seen when patients are treated with conventional therapy alone.

详细描述

Objective(s): The objective of this study is to analyze a data from a study that examined the biotherapeutic effect of combining conventional therapy in the presence of MGN-3/Biobran. The study focused on treatment of patients in Vietnam with hepatocellular carcinoma (HCC) and Hepatitis B and C.

Purpose of the study:

Aim 1: The biotherapeutic effect of combining conventional therapy and a natural, non-toxic arabinoxylan rice bran (MGN-3/Biobran) for the treatment of patients with HCC will be examined. Parameters under investigation include, lifespan of the patient, progression of the disease (tumor size), and recurrence of the disease.

Aim 2: The biotherapeutic effect of combining conventional therapy and a natural, non-toxic arabinoxylan rice bran (MGN-3/Biobran) for the treatment of patients with Hepatitis B virus (HBV) will be examined. Parameters under investigation include alanine transaminase (ALT) levels, HBV antigen levels, and HBV DNA levels.

Methodology:

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

入选标准

  • 未提供

排除标准

  • 未提供

研究组 & 干预措施

Conventional Therapy plus MGN-3

Experimental

干预措施: TOCE plus RFA (Procedure)

Conventional Therapy

Active Comparator

Conventional therapy is given, including PEIT, TOCE, PEIT + TOCE, TOCE + RFA for hepatocellular carcinoma or Entecavir for hepatitis B virus.

干预措施: PEIT (Procedure)

Conventional Therapy

Active Comparator

Conventional therapy is given, including PEIT, TOCE, PEIT + TOCE, TOCE + RFA for hepatocellular carcinoma or Entecavir for hepatitis B virus.

干预措施: TOCE (Procedure)

Conventional Therapy

Active Comparator

Conventional therapy is given, including PEIT, TOCE, PEIT + TOCE, TOCE + RFA for hepatocellular carcinoma or Entecavir for hepatitis B virus.

干预措施: TOCE plus PEIT (Procedure)

Conventional Therapy

Active Comparator

Conventional therapy is given, including PEIT, TOCE, PEIT + TOCE, TOCE + RFA for hepatocellular carcinoma or Entecavir for hepatitis B virus.

干预措施: TOCE plus RFA (Procedure)

Conventional Therapy

Active Comparator

Conventional therapy is given, including PEIT, TOCE, PEIT + TOCE, TOCE + RFA for hepatocellular carcinoma or Entecavir for hepatitis B virus.

干预措施: Entecavir (Drug)

Conventional Therapy plus MGN-3

Experimental

干预措施: PEIT (Procedure)

Conventional Therapy plus MGN-3

Experimental

干预措施: TOCE (Procedure)

Conventional Therapy plus MGN-3

Experimental

干预措施: TOCE plus PEIT (Procedure)

Conventional Therapy plus MGN-3

Experimental

干预措施: MGN-3 (Dietary Supplement)

Conventional Therapy plus MGN-3

Experimental

干预措施: Entecavir (Drug)

结局指标

主要结局

Patient survival

时间窗: 3 years

次要结局

  • Disease recurrence(3 years)

研究者

发起方
The 108 Military Central Hospital
申办方类型
Other Gov

研究点 (1)

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