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한의약융합데이터센터


근거중심한의약 DB

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Title

Coriolus versicolor (Yunzhi) Use as Therapy in Advanced Hepatocellular Carcinoma Patients with Poor Liver Function or Who Are Unfit for Standard Therapy.

Authors

Chay WY, Tham CK, Toh HC, Lim HY, Tan CK, Lim C, Wang WW, Choo SP.

Journal

J Altern Complement Med.

Year

2017

Vol (Issue)

23(8)

Page

648-52.

doi

10.1089/acm.2016.0136.

PMID

28375640

Url

http://www.ncbi.nlm.nih.gov/pubmed/28375640

MeSH

Aged
Basidiomycota*
Biological Products/therapeutic use*
Carcinoma, Hepatocellular/drug therapy*
Carcinoma, Hepatocellular/physiopathology
Female
Humans
Liver/physiopathology
Liver Neoplasms/drug therapy*
Liver Neoplasms/physiopathology
Male
Middle Aged

Keywords

Coriolus versicolor; hepatocellular carcinoma; medicinal mushrooms; polysaccharides; quality of life; yunzhi

한글 키워드

운지버섯; 간세포 암종; 약용버섯; 다당류; 삶의 질; 운지버섯

KMCRIC
Summary & Commentary

KMCRIC 비평 보기 +

Korean Study

Abstract

BACKGROUND:
The majority of patients with hepatocellular carcinoma (HCC) are inoperable and results with conventional chemotherapy are dismal. Many end up with no treatment options and resort to alternative medicine. The authors report the use of Coriolus versicolor (CV) in advanced HCC patients with poor liver function or who were unfit to receive standard therapy.

METHODS:
Fifteen eligible cases were randomized 2:1 to either CV or placebo. The primary endpoint was the median time to progression (TTP) between both arms. Secondary endpoints include evaluating response rates, toxicity, quality of life (QOL), progression-free survival (PFS), and overall survival (OS). Further correlative studies were performed looking at the effect of CV on the immune system.

RESULTS:
The median treatment duration was 1.5 cycles and 3 cycles on the placebo and CV arm, respectively. Median TTP was 2.5 (1.4-5.3) months compared to 4.2 (0.4-4.2) months in the CV and placebo arm, respectively, hazard ratio (HR) 0.70 (0.16-3.05 p = 0.634). Median PFS was 2.5 (1.4-5.3) months in the CV and 1.1 (0.4-4.2) months in the placebo arm, HR 0.42 (0.13-1.34, p = 0.144). Median OS was 6.5 (3.3-24.1) and 2.2 (0.8-23.3) months, respectively, HR 0.35 (0.10-1.25, p = 0.105). Social and emotional functioning scores were higher in the CV group compared to placebo group on treatment. CV subjects had less appetite loss and pain symptoms compared to placebo subjects during treatment.

CONCLUSIONS:
There was no difference in TTP with use of CV compared to placebo. CV subjects generally had better QOL on treatment compared to placebo subjects. The utility of this supplement in patients whose primary treatment goal is palliation should be further explored.

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