Postoperative use of the chemopreventive vitamin K2 analog in patients with hepatocellular carcinoma.

<h4>Aim</h4>To evaluate the chemopreventive efficacy of vitamin K2 (VK2) analog in patients with hepatocellular carcinoma (HCC) after curative hepatic resection or local ablation, since a recent randomized control trial (RCT) and systematic review have given contradictory results.<h4&...

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Main Authors: Jian-Hong Zhong, Xin-Shao Mo, Bang-De Xiang, Wei-Ping Yuan, Jin-Fang Jiang, Gui-Sheng Xie, Le-Qun Li
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2013-01-01
Series:PLoS ONE
Online Access:https://www.ncbi.nlm.nih.gov/pmc/articles/pmid/23505456/?tool=EBI
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author Jian-Hong Zhong
Xin-Shao Mo
Bang-De Xiang
Wei-Ping Yuan
Jin-Fang Jiang
Gui-Sheng Xie
Le-Qun Li
author_facet Jian-Hong Zhong
Xin-Shao Mo
Bang-De Xiang
Wei-Ping Yuan
Jin-Fang Jiang
Gui-Sheng Xie
Le-Qun Li
author_sort Jian-Hong Zhong
collection DOAJ
description <h4>Aim</h4>To evaluate the chemopreventive efficacy of vitamin K2 (VK2) analog in patients with hepatocellular carcinoma (HCC) after curative hepatic resection or local ablation, since a recent randomized control trial (RCT) and systematic review have given contradictory results.<h4>Methods</h4>MEDLINE, EMBASE and Cochrane library databases were systematically searched through the end of May 2012. Meta-analysis of RCTs and cohort studies was performed to estimate the effects of the VK2 analog on tumor recurrence rate and overall survival (OS). Risk ratios (RRs) and 95% confidence intervals (95% CIs) were calculated.<h4>Results</h4>Six RCTs and one cohort study involving a total of 930 patients were included. VK2 analog therapy did not reduce the 1-year recurrence rate, with a pooled RR of 0.67 (95% CI 0.39-1.13, p = 0.13). However, VK2 analog therapy was associated with a significant reduction in the 2- and 3-year tumor recurrence rates, with respective pooled RRs of 0.65 (95% CI 0.51-0.83, p<0.001) and 0.70 (95% CI = 0.58-0.85, p<0.001). The therapy was also associated with a significant improvement in 1-, 2-, and 3-year OS, with respective pooled RRs of 1.03 (95% CI 1.01-1.05, p = 0.02), 1.11 (95% CI 1.03-1.19, p = 0.005) and 1.14 (95% CI 1.02-1.28, p = 0.02). None of the studies reported adverse effects attributable to VK2 analog therapy.<h4>Conclusion</h4>The VK2 analog may reduce recurrence rate after 1 year and improve OS in HCC patients as early as 1 year. However, these findings should be considered preliminary since the majority of patients came from an RCT with survival data out to only 1 year. More extensive studies with larger sample sizes and longer follow-up are needed.
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spelling doaj.art-d68bf9e1c45f430bac18b6bbf9b63b4b2022-12-21T23:41:05ZengPublic Library of Science (PLoS)PLoS ONE1932-62032013-01-0183e5808210.1371/journal.pone.0058082Postoperative use of the chemopreventive vitamin K2 analog in patients with hepatocellular carcinoma.Jian-Hong ZhongXin-Shao MoBang-De XiangWei-Ping YuanJin-Fang JiangGui-Sheng XieLe-Qun Li<h4>Aim</h4>To evaluate the chemopreventive efficacy of vitamin K2 (VK2) analog in patients with hepatocellular carcinoma (HCC) after curative hepatic resection or local ablation, since a recent randomized control trial (RCT) and systematic review have given contradictory results.<h4>Methods</h4>MEDLINE, EMBASE and Cochrane library databases were systematically searched through the end of May 2012. Meta-analysis of RCTs and cohort studies was performed to estimate the effects of the VK2 analog on tumor recurrence rate and overall survival (OS). Risk ratios (RRs) and 95% confidence intervals (95% CIs) were calculated.<h4>Results</h4>Six RCTs and one cohort study involving a total of 930 patients were included. VK2 analog therapy did not reduce the 1-year recurrence rate, with a pooled RR of 0.67 (95% CI 0.39-1.13, p = 0.13). However, VK2 analog therapy was associated with a significant reduction in the 2- and 3-year tumor recurrence rates, with respective pooled RRs of 0.65 (95% CI 0.51-0.83, p<0.001) and 0.70 (95% CI = 0.58-0.85, p<0.001). The therapy was also associated with a significant improvement in 1-, 2-, and 3-year OS, with respective pooled RRs of 1.03 (95% CI 1.01-1.05, p = 0.02), 1.11 (95% CI 1.03-1.19, p = 0.005) and 1.14 (95% CI 1.02-1.28, p = 0.02). None of the studies reported adverse effects attributable to VK2 analog therapy.<h4>Conclusion</h4>The VK2 analog may reduce recurrence rate after 1 year and improve OS in HCC patients as early as 1 year. However, these findings should be considered preliminary since the majority of patients came from an RCT with survival data out to only 1 year. More extensive studies with larger sample sizes and longer follow-up are needed.https://www.ncbi.nlm.nih.gov/pmc/articles/pmid/23505456/?tool=EBI
spellingShingle Jian-Hong Zhong
Xin-Shao Mo
Bang-De Xiang
Wei-Ping Yuan
Jin-Fang Jiang
Gui-Sheng Xie
Le-Qun Li
Postoperative use of the chemopreventive vitamin K2 analog in patients with hepatocellular carcinoma.
PLoS ONE
title Postoperative use of the chemopreventive vitamin K2 analog in patients with hepatocellular carcinoma.
title_full Postoperative use of the chemopreventive vitamin K2 analog in patients with hepatocellular carcinoma.
title_fullStr Postoperative use of the chemopreventive vitamin K2 analog in patients with hepatocellular carcinoma.
title_full_unstemmed Postoperative use of the chemopreventive vitamin K2 analog in patients with hepatocellular carcinoma.
title_short Postoperative use of the chemopreventive vitamin K2 analog in patients with hepatocellular carcinoma.
title_sort postoperative use of the chemopreventive vitamin k2 analog in patients with hepatocellular carcinoma
url https://www.ncbi.nlm.nih.gov/pmc/articles/pmid/23505456/?tool=EBI
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