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Variceal bleeding is aggravated by portal venous invasion of hepatocellular carcinoma: a matched nested case-control study

BACKGROUND: We hypothesized that portal vein tumor thrombosis (PVTT) in hepatocellular carcinoma (HCC) increases portal pressure and causes esophageal varices and variceal bleedings. We examined the incidence of high-risk varices and variceal bleeding and determined the indications for variceal scre...

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Autores principales: Lim, Jihye, Kim, Ha Il, Kim, Eunju, Kim, Jiyoon, An, Jihyun, Chang, Seheon, Kim, Seon-Ok, Lee, Han chu, Lee, Yung Sang, Shim, Ju Hyun
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7786454/
https://www.ncbi.nlm.nih.gov/pubmed/33402105
http://dx.doi.org/10.1186/s12885-020-07708-1
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author Lim, Jihye
Kim, Ha Il
Kim, Eunju
Kim, Jiyoon
An, Jihyun
Chang, Seheon
Kim, Seon-Ok
Lee, Han chu
Lee, Yung Sang
Shim, Ju Hyun
author_facet Lim, Jihye
Kim, Ha Il
Kim, Eunju
Kim, Jiyoon
An, Jihyun
Chang, Seheon
Kim, Seon-Ok
Lee, Han chu
Lee, Yung Sang
Shim, Ju Hyun
author_sort Lim, Jihye
collection PubMed
description BACKGROUND: We hypothesized that portal vein tumor thrombosis (PVTT) in hepatocellular carcinoma (HCC) increases portal pressure and causes esophageal varices and variceal bleedings. We examined the incidence of high-risk varices and variceal bleeding and determined the indications for variceal screening and prophylaxis. METHODS: This study included 1709 asymptomatic patients without any prior history of variceal hemorrhage or endoscopic prophylaxis who underwent upper endoscopy within 30 days before or after initial anti-HCC treatment. Of these patients, 206 had PVTT, and after 1:2 individual matching, 161 of them were matched with 309 patients without PVTT. High-risk varices were defined as large/medium varices or small varices with red-color signs and variceal bleeding. Bleeding rates from the varices were compared between matched pairs. Risk factors for variceal bleeding in the entire set of patients with PVTT were also explored. RESULTS: In the matched-pair analysis, the proportion of high-risk varices at screening (23.0% vs. 13.3%; P = 0.003) and the cumulative rate of variceal bleeding (4.5% vs. 0.4% at 1 year; P = 0.009) were significantly greater in the PVTT group. Prolonged prothrombin time, lower platelet count, presence of extrahepatic metastasis, and Vp4 PVTT were independent risk factors related to high-risk varices in the total set of 206 patients with PVTT (Adjusted odds ratios [95% CIs], 1.662 [1.151–2.401]; 0.985 [0.978–0.993]; 4.240 [1.783–10.084]; and 3.345 [1.457–7.680], respectively; Ps < 0.05). During a median follow-up of 43.2 months, 10 patients with PVTT experienced variceal bleeding episodes, 9 of whom (90%) had high-risk varices. Presence of high-risk varices and sorafenib use for HCC treatment were significant predictors of variceal bleeding in the complete set of patients with PVTT (Adjusted hazard ratios [95% CIs], 26.432 [3.230–216.289]; and 5.676 [1.273–25.300], respectively; Ps < 0.05). CONCLUSIONS: PVTT in HCC appears to increase the likelihood of high-risk varices and variceal bleeding. In HCC patients with PVTT, endoscopic prevention could be considered, at least in high-risk variceal carriers taking sorafenib.
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spelling pubmed-77864542021-01-07 Variceal bleeding is aggravated by portal venous invasion of hepatocellular carcinoma: a matched nested case-control study Lim, Jihye Kim, Ha Il Kim, Eunju Kim, Jiyoon An, Jihyun Chang, Seheon Kim, Seon-Ok Lee, Han chu Lee, Yung Sang Shim, Ju Hyun BMC Cancer Research Article BACKGROUND: We hypothesized that portal vein tumor thrombosis (PVTT) in hepatocellular carcinoma (HCC) increases portal pressure and causes esophageal varices and variceal bleedings. We examined the incidence of high-risk varices and variceal bleeding and determined the indications for variceal screening and prophylaxis. METHODS: This study included 1709 asymptomatic patients without any prior history of variceal hemorrhage or endoscopic prophylaxis who underwent upper endoscopy within 30 days before or after initial anti-HCC treatment. Of these patients, 206 had PVTT, and after 1:2 individual matching, 161 of them were matched with 309 patients without PVTT. High-risk varices were defined as large/medium varices or small varices with red-color signs and variceal bleeding. Bleeding rates from the varices were compared between matched pairs. Risk factors for variceal bleeding in the entire set of patients with PVTT were also explored. RESULTS: In the matched-pair analysis, the proportion of high-risk varices at screening (23.0% vs. 13.3%; P = 0.003) and the cumulative rate of variceal bleeding (4.5% vs. 0.4% at 1 year; P = 0.009) were significantly greater in the PVTT group. Prolonged prothrombin time, lower platelet count, presence of extrahepatic metastasis, and Vp4 PVTT were independent risk factors related to high-risk varices in the total set of 206 patients with PVTT (Adjusted odds ratios [95% CIs], 1.662 [1.151–2.401]; 0.985 [0.978–0.993]; 4.240 [1.783–10.084]; and 3.345 [1.457–7.680], respectively; Ps < 0.05). During a median follow-up of 43.2 months, 10 patients with PVTT experienced variceal bleeding episodes, 9 of whom (90%) had high-risk varices. Presence of high-risk varices and sorafenib use for HCC treatment were significant predictors of variceal bleeding in the complete set of patients with PVTT (Adjusted hazard ratios [95% CIs], 26.432 [3.230–216.289]; and 5.676 [1.273–25.300], respectively; Ps < 0.05). CONCLUSIONS: PVTT in HCC appears to increase the likelihood of high-risk varices and variceal bleeding. In HCC patients with PVTT, endoscopic prevention could be considered, at least in high-risk variceal carriers taking sorafenib. BioMed Central 2021-01-05 /pmc/articles/PMC7786454/ /pubmed/33402105 http://dx.doi.org/10.1186/s12885-020-07708-1 Text en © The Author(s) 2020 Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated in a credit line to the data.
spellingShingle Research Article
Lim, Jihye
Kim, Ha Il
Kim, Eunju
Kim, Jiyoon
An, Jihyun
Chang, Seheon
Kim, Seon-Ok
Lee, Han chu
Lee, Yung Sang
Shim, Ju Hyun
Variceal bleeding is aggravated by portal venous invasion of hepatocellular carcinoma: a matched nested case-control study
title Variceal bleeding is aggravated by portal venous invasion of hepatocellular carcinoma: a matched nested case-control study
title_full Variceal bleeding is aggravated by portal venous invasion of hepatocellular carcinoma: a matched nested case-control study
title_fullStr Variceal bleeding is aggravated by portal venous invasion of hepatocellular carcinoma: a matched nested case-control study
title_full_unstemmed Variceal bleeding is aggravated by portal venous invasion of hepatocellular carcinoma: a matched nested case-control study
title_short Variceal bleeding is aggravated by portal venous invasion of hepatocellular carcinoma: a matched nested case-control study
title_sort variceal bleeding is aggravated by portal venous invasion of hepatocellular carcinoma: a matched nested case-control study
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7786454/
https://www.ncbi.nlm.nih.gov/pubmed/33402105
http://dx.doi.org/10.1186/s12885-020-07708-1
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