the Efficacy and Safety of Ginsenoside Rg3 Capsule in Prevention of Postoperative Recurrence of Hepatocellular Carcinoma

NCT ID: NCT01717066

Last Updated: 2016-03-31

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

COMPLETED

Clinical Phase

NA

Total Enrollment

480 participants

Study Classification

INTERVENTIONAL

Study Start Date

2012-04-30

Study Completion Date

2015-05-31

Brief Summary

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Using the subject with hepatocellular carcinoma in the conventional therapy to evaluate the efficacy and safety of ginsenoside Rg3 (20mg BID) and placebo in prevention and treatment of postoperative recurrence of liver cancer,respectively

Detailed Description

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1. Randomized, double-blind, multi-center, placebo-controlled, parallel-group;
2. Subject population: patients undergone radical resection of hepatocellular carcinoma;
3. Active drug group:

Ginsenoside Rg3 group: general treatment + ginsenoside Rg3 Control group (placebo group): general treatment + placebo 4.Method of group assignment: 5research centers, central-block-stratified randomization, a ratio of active drug group to control group: 2:1 5.Dose and mode of administration: Ginsenoside Rg3 group: ginsenoside Rg3 20mg BID, two months as one cycle, continue until recurrence occurs Placebo Group: placebo, 2 capsules, BID, continue until recurrence occurs 6.Study period: Screening phase: screening for enrollment within 8 weeks after the radical resection Follow up: review every 2-3 months following the surgery Post-trial investigation: within 28 days after the trial is ended or the recurrence occurs

Conditions

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Stage I Hepatocellular Carcinoma Stage II Hepatocellular Carcinoma

Study Design

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Allocation Method

RANDOMIZED

Intervention Model

PARALLEL

Primary Study Purpose

PREVENTION

Blinding Strategy

DOUBLE

Participants Investigators

Study Groups

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the ginsenoside Rg3

320 HCCs,the ginsenoside Rg3 capsule,4-8 weeks after surgery, will be taken, 2 capsules, BID, 8 weeks as one cycle, continue taking it until the tumor recurs or until the end date of the study for patients without recurrence

Group Type EXPERIMENTAL

the ginsenoside Rg3

Intervention Type DRUG

the placebo

160 HCCs as control group with patients who don't receive any adjuvant therapy after liver resection, to compare with the treatment group

Group Type PLACEBO_COMPARATOR

Placebo

Intervention Type DRUG

Interventions

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the ginsenoside Rg3

Intervention Type DRUG

Placebo

Intervention Type DRUG

Other Intervention Names

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Shen Yi capsule

Eligibility Criteria

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Inclusion Criteria

* 18-75 years old,male and female
* Mainly based on the criteria for liver cancer TNM stage I and II (edition 7) and BCLC stage A, the following needs to be satisfied:

1. individual tumor larger than or equal to 2 cm and smaller than or equal to 10 cm in the maximum diameter
2. multiple tumors with no more than three tumors
3. No macroscopic tumor embolus
* ECOG performance state is 0-1
* Child-Pugh grade is A
* The clinical review confirms the absence of recurrence within 8 weeks before the enrollment
* Sign the informed consent

Exclusion Criteria

* Pregnant and breast-feeding women
* Patients with severe diseases in the brain, heart,lungs, kidneys and hematological system
* Patients who have received other anti-tumor therapies before the surgery (including liver transplantation, TACE, local tumor ablation, chemotherapy, radiotherapy, molecular targeted therapy and other anti-tumor therapy)
* DDS chemotherapy pump placed in the portal vein during the surgery
* Patients who are participating in other drug trials
* Patients known or suspected to be allergic to ginsenoside, with a history of allergy to biological preparations, allergic constitution or currently in an allergic state;
* With active severe clinical infection
* Epilepsy episode which needs drug therapy
* With a history of allotransplantation;
* With a previous history of tumor in other systems, but except for:

1. Carcinoma in situ of cervix
2. Basal cell carcinoma after treatment,Superficial bladder cancer (Ta, Tis and T1
3. Any cancer after curative treatment no less than three years ago
* Patients with signs or a history of bleeding diathesis
* Patients currently receiving kidney dialysis
* A history of bleeding in the gastrointestinal tract within 30 days, or severe gastroesophageal varices with red signs; with a history of gastroesophageal variceal hemorrhage
* Recurrent HCC
* Patients unable to take drug orally
* Patients inappropriate to participate in the trial upon the investigator's judgment
Minimum Eligible Age

18 Years

Maximum Eligible Age

75 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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Huazhong University of Science and Technology

OTHER

Sponsor Role collaborator

Shanghai Zhongshan Hospital

OTHER

Sponsor Role collaborator

Sun Yat-sen University

OTHER

Sponsor Role collaborator

First Affiliated Hospital of Harbin Medical University

OTHER

Sponsor Role collaborator

First Affiliated Hospital of Fujian Medical University

OTHER

Sponsor Role collaborator

ShenFeng

OTHER

Sponsor Role lead

Responsible Party

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ShenFeng

vice president of the Eastern Hepatobiliary Surgery Hospital

Responsibility Role SPONSOR_INVESTIGATOR

Principal Investigators

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Feng Shen, MD,PhD

Role: PRINCIPAL_INVESTIGATOR

Eastern Hepatobiliary Surgery Hospital

Locations

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The First Affiliated Hospital of Fujian Medical University

Fuzhou, Fujian, China

Site Status

Tumor Hospital,Sun Yat-san University

Guangzhou, Guangdong, China

Site Status

The First Affiliated Hospital of Harbin Medical University

Harbin, Heilongjiang, China

Site Status

Tongji Hospital,Huazhong University of Science & Technology

Wuhan, Hubei, China

Site Status

Zhongshan hospital,Fudan University

Shanghai, , China

Site Status

Countries

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China

References

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Yue PY, Wong DY, Wu PK, Leung PY, Mak NK, Yeung HW, Liu L, Cai Z, Jiang ZH, Fan TP, Wong RN. The angiosuppressive effects of 20(R)- ginsenoside Rg3. Biochem Pharmacol. 2006 Aug 14;72(4):437-45. doi: 10.1016/j.bcp.2006.04.034. Epub 2006 May 12.

Reference Type BACKGROUND
PMID: 16793023 (View on PubMed)

Liu TG, Huang Y, Cui DD, Huang XB, Mao SH, Ji LL, Song HB, Yi C. Inhibitory effect of ginsenoside Rg3 combined with gemcitabine on angiogenesis and growth of lung cancer in mice. BMC Cancer. 2009 Jul 23;9:250. doi: 10.1186/1471-2407-9-250.

Reference Type BACKGROUND
PMID: 19624862 (View on PubMed)

Zhang Q, Kang X, Yang B, Wang J, Yang F. Antiangiogenic effect of capecitabine combined with ginsenoside Rg3 on breast cancer in mice. Cancer Biother Radiopharm. 2008 Oct;23(5):647-53. doi: 10.1089/cbr.2008.0532.

Reference Type BACKGROUND
PMID: 18999937 (View on PubMed)

Xu TM, Cui MH, Xin Y, Gu LP, Jiang X, Su MM, Wang DD, Wang WJ. Inhibitory effect of ginsenoside Rg3 on ovarian cancer metastasis. Chin Med J (Engl). 2008 Aug 5;121(15):1394-7.

Reference Type BACKGROUND
PMID: 18959116 (View on PubMed)

Iishi H, Tatsuta M, Baba M, Uehara H, Nakaizumi A, Shinkai K, Akedo H, Funai H, Ishiguro S, Kitagawa I. Inhibition by ginsenoside Rg3 of bombesin-enhanced peritoneal metastasis of intestinal adenocarcinomas induced by azoxymethane in Wistar rats. Clin Exp Metastasis. 1997 Nov;15(6):603-11. doi: 10.1023/a:1018491314066.

Reference Type BACKGROUND
PMID: 9344044 (View on PubMed)

Lee JY, Jung KH, Morgan MJ, Kang YR, Lee HS, Koo GB, Hong SS, Kwon SW, Kim YS. Sensitization of TRAIL-induced cell death by 20(S)-ginsenoside Rg3 via CHOP-mediated DR5 upregulation in human hepatocellular carcinoma cells. Mol Cancer Ther. 2013 Mar;12(3):274-85. doi: 10.1158/1535-7163.MCT-12-0054. Epub 2012 Oct 10.

Reference Type BACKGROUND
PMID: 23053497 (View on PubMed)

Zhang C, Liu L, Yu Y, Chen B, Tang C, Li X. Antitumor effects of ginsenoside Rg3 on human hepatocellular carcinoma cells. Mol Med Rep. 2012 May;5(5):1295-8. doi: 10.3892/mmr.2012.808. Epub 2012 Feb 23.

Reference Type BACKGROUND
PMID: 22366885 (View on PubMed)

Park HM, Kim SJ, Kim JS, Kang HS. Reactive oxygen species mediated ginsenoside Rg3- and Rh2-induced apoptosis in hepatoma cells through mitochondrial signaling pathways. Food Chem Toxicol. 2012 Aug;50(8):2736-41. doi: 10.1016/j.fct.2012.05.027. Epub 2012 May 22.

Reference Type BACKGROUND
PMID: 22634290 (View on PubMed)

Other Identifiers

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EHBH-RCT-2011-002

Identifier Type: -

Identifier Source: org_study_id

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