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

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dc.contributor.authorLim, Jihye-
dc.contributor.authorKim, Ha Il-
dc.contributor.authorKim, Eunju-
dc.contributor.authorKim, Jiyoon-
dc.contributor.authorAn, Jihyun-
dc.contributor.authorChang, Seheon-
dc.contributor.authorKim, Seon-Ok-
dc.contributor.authorLee, Han Chu-
dc.contributor.authorLee, Yung Sang-
dc.contributor.authorShim, Ju Hyun-
dc.date.accessioned2021-08-02T08:27:53Z-
dc.date.available2021-08-02T08:27:53Z-
dc.date.created2021-05-11-
dc.date.issued2021-01-
dc.identifier.issn1471-2407-
dc.identifier.urihttps://scholarworks.bwise.kr/hanyang/handle/2021.sw.hanyang/8102-
dc.description.abstractBackground 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.-
dc.language영어-
dc.language.isoen-
dc.publisherBMC-
dc.titleVariceal bleeding is aggravated by portal venous invasion of hepatocellular carcinoma: a matched nested case-control study-
dc.typeArticle-
dc.contributor.affiliatedAuthorAn, Jihyun-
dc.identifier.doi10.1186/s12885-020-07708-1-
dc.identifier.scopusid2-s2.0-85098688240-
dc.identifier.wosid000608023000026-
dc.identifier.bibliographicCitationBMC CANCER, v.21, no.1, pp.1 - 10-
dc.relation.isPartOfBMC CANCER-
dc.citation.titleBMC CANCER-
dc.citation.volume21-
dc.citation.number1-
dc.citation.startPage1-
dc.citation.endPage10-
dc.type.rimsART-
dc.type.docTypeArticle-
dc.description.journalClass1-
dc.description.isOpenAccessY-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.relation.journalResearchAreaOncology-
dc.relation.journalWebOfScienceCategoryOncology-
dc.subject.keywordPlussorafenib-
dc.subject.keywordPlusadult-
dc.subject.keywordPlusArticle-
dc.subject.keywordPlusasymptomatic disease-
dc.subject.keywordPluscase control study-
dc.subject.keywordPlusclinical effectiveness-
dc.subject.keywordPlusclinical feature-
dc.subject.keywordPluscontrolled study-
dc.subject.keywordPlusdigestive tract endoscopy-
dc.subject.keywordPlusdrug effect-
dc.subject.keywordPlusdrug efficacy-
dc.subject.keywordPlusdrug response-
dc.subject.keywordPlusfemale-
dc.subject.keywordPlusfollow up-
dc.subject.keywordPlushepatic portal vein-
dc.subject.keywordPlushigh risk patient-
dc.subject.keywordPlushuman-
dc.subject.keywordPlusincidence-
dc.subject.keywordPlusliver cell carcinoma-
dc.subject.keywordPlusliver metastasis-
dc.subject.keywordPlusmajor clinical study-
dc.subject.keywordPlusmale-
dc.subject.keywordPlusmiddle aged-
dc.subject.keywordPlusplatelet count-
dc.subject.keywordPlusportal vein tumor thrombosis-
dc.subject.keywordPlusprothrombin time-
dc.subject.keywordPlusrisk factor-
dc.subject.keywordPlustreatment outcome-
dc.subject.keywordPlustumor invasion-
dc.subject.keywordPlustumor thrombus-
dc.subject.keywordPlusvariceal bleeding-
dc.subject.keywordPlusvein disease-
dc.subject.keywordPluscomplication-
dc.subject.keywordPlusesophagus varices-
dc.subject.keywordPlusgastrointestinal hemorrhage-
dc.subject.keywordPlushepatic portal vein-
dc.subject.keywordPlusliver cell carcinoma-
dc.subject.keywordPlusliver tumor-
dc.subject.keywordPluspathology-
dc.subject.keywordPlusprognosis-
dc.subject.keywordPlussurvival rate-
dc.subject.keywordPlustumor invasion-
dc.subject.keywordAuthorHepatocellular carcinoma-
dc.subject.keywordAuthorPortal vein thrombosis-
dc.subject.keywordAuthorEsophageal varices-
dc.subject.keywordAuthorVariceal bleeding-
dc.subject.keywordAuthorRisk factor-
dc.identifier.urlhttps://bmccancer.biomedcentral.com/articles/10.1186/s12885-020-07708-1-
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