Coriolus Versicolor as Palliative Therapy Compared to Placebo in Patients With Child-Pugh C Unresectable Hepatocellular Carcinoma

Sponsor

National University Hospital, Singapore (Other)

Overall Status

Terminated

CT.gov ID

NCT01097083

Collaborator

(none)

Enrollment

Locations

Duration (Months)

6.7

Patients Per Site

0.2

Patients Per Site Per Month

Study Details

Study Description

Brief Summary

The hypothesis of this study is that the median time to progression in the experimental arm is 2 months as compared to the placebo arm of 1.4 months

Condition or Disease	Intervention/Treatment	Phase
Carcinoma Therapy	Drug: Coriolus Versicolor	Phase 2

Study Design

Study Type:

Interventional

Allocation:

Randomized

Primary Purpose:

Treatment

Official Title:

A Randomized Phase II Trial of Coriolus Versicolor as Palliative Therapy Compared to Placebo in Patients With Child-Pugh C Unresectable Hepatocellular Carcinoma or Who Are Unfit for Standard Therapy

Study Start Date :

Apr 1, 2010

Actual Primary Completion Date :

Oct 1, 2013

Actual Study Completion Date :

Oct 1, 2013

Outcome Measures

Primary Outcome Measures

Eligibility Criteria

Criteria

Ages Eligible for Study:

21 Years and Older

Sexes Eligible for Study:

All

Accepts Healthy Volunteers:

Inclusion Criteria:

The diagnosis of HCC is made either by histological examination of tumor tissue or imaging evidence of a typical space-occupying lesion in the liver together with a serum AFP concentration of above 500 ng/ml (normal value, 10 ng/ml) in a known carrier of hepatitis B or C, or AFP above 400 ng/ml in non Hepatitis B or C carrier.

Patients with unresectable HCC that is not amenable to liver transplantation nor local ablative technique and who are not suitable for any conventional systemic therapy (including sorafenib and chemotherapy).
Patients with Child-Pugh Class C liver cirrhosis (Child-Pugh Scores of 10-15 points). Patients with Child-Pugh Class A or B liver cirrhosis who are not eligible for conventional therapy or other clinical trials or who refuse conventional therapy are included
Life Expectancy of at least 12 weeks
All patients should have anti-HBc antibodies tested if HBs Ag is negative. If anti-HBc is positive, HBV DNA detection should be performed to determine viral load. An undetectable Hep B DNA level (DNA levels < 12 IU/ml) in the presence of a positive Hep B core total antibody would indicate no active hepatitis infection and the subject would still be eligible for this trial.
Age >21 years.
Performance status ECOG 0 - 2
Patients must have normal organ and marrow function as defined below:

Absolute neutrophil count > 1.5 x 109/L Platelets > 50 x 109/L Haemoglobin > 9.0g/dl Total bilirubin < 51umol/L (3 mg /dL) AST (SGOT)/ALT (SGPT) < 5 X institutional ULN Creatinine < 1.5 ULN INR <1.7 or prothrombin time (PT) <4 seconds above ULN

Patients who have not received any local or systemic treatment in the last 4 weeks.
Measurable disease according to RECIST
Ability to understand and the willingness to sign a written informed consent document.
Ability to swallow oral medication
The effects of C versicolor on the developing human fetus are unknown. For this reason, woman of child-bearing potential and men must agree to use adequate contraception (hormonal or barrier method of birth control; abstinence) prior to study entry and for the duration of study participation. Should a woman become pregnant or suspect she is pregnant while participating in this study, she should inform her treating physician immediately.

Exclusion Criteria:

Patients with a history of prior malignancy that is distinct in site and histology from HCC except non-melanoma skin cancer. Any cancer curatively treated more than 3 years prior to entry is permitted.
Uncontrolled intercurrent illness including, but not limited to, ongoing or active infection, symptomatic congestive heart failure, unstable angina pectoris, cardiac arrhythmia, intractable ascites that could not be controlled by medical therapy
Prior use of C versicolor or Yunzhi for HCC
Patients who have had chemotherapy or radiotherapy within 4 weeks prior to entering the study or those who have not recovered from adverse events due to agents administered more than 4 weeks earlier
Patients who are using other chinese herbal therapies concurrently or on any other investigation agents for treatment of their cancer
Known of history of allergic reactions attributed to compounds of similar chemical or biologic composition used in the study.
Presence of active hepatitis B/C flare.
Known history of Human Immunodeficiency Virus (HIV) Infection
Gastrointestinal disease which could affect the absorption or pharmacokinetics of the study drug as determined by investigator
Psychiatric illness/social situations that would limit compliance with study requirements. Patients with severe depression or psychiatric disorders will be excluded.
Known alcohol and/or substance abuser that may interfere with the subject's participation in the study or evaluation of study results.
Pregnancy or breast-feeding subjects. All female patients with reproductive potential must have a negative pregnancy test (serum or urine) within the 14 days prior to study enrollment and must be willing to use adequate contraception
Patients suffering from autoimmune disease, patients on concomitant long-term immunosuppressant therapy and those scheduled to receive bone marrow transplants

Contacts and Locations

Locations

	Site	City	Country	Postal Code
1	National University Hospital	Singapore	Singapore	119074
2	Singapore General Hospital	Singapore	Singapore	169608
3	National Cancer Centre	Singapore	Singapore	169610

Sponsors and Collaborators

National University Hospital, Singapore

Investigators

Principal Investigator: Wei Peng Yong, MRCP, MB ChB', National University Hospital, Singapore
Principal Investigator: Choo Su Pin, BMBS, MRCP, M Med, National Cancer Centre
Principal Investigator: Tan Chee Kiat, MBBS, FRCP, FAMS, Singapore General Hospital