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A Proposal for Modification of the Barcelona Clinic Liver Cancer Staging System Considering the Prognostic Implication of Performance Status

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dc.contributor.authorCho, HJ-
dc.contributor.authorKim, SS-
dc.contributor.authorKang, SY-
dc.contributor.authorYang, MJ-
dc.contributor.authorNoh, CK-
dc.contributor.authorHwang, JC-
dc.contributor.authorLim, SG-
dc.contributor.authorShin, SJ-
dc.contributor.authorLee, KM-
dc.contributor.authorYoo, BM-
dc.contributor.authorLee, KJ-
dc.contributor.authorKim, JH-
dc.contributor.authorCho, SW-
dc.contributor.authorCheong, JY-
dc.contributor.authorKorean Liver Cancer Association-
dc.date.accessioned2020-10-21T07:21:33Z-
dc.date.available2020-10-21T07:21:33Z-
dc.date.issued2019-
dc.identifier.issn1976-2283-
dc.identifier.urihttp://repository.ajou.ac.kr/handle/201003/18940-
dc.description.abstractBACKGROUND/AIMS: Barcelona Clinic Liver Cancer (BCLC) C stage demonstrates considerable heterogeneity because it includes patients with either symptomatic tumors (performance status [PS], 1-2) or with an invasive tumoral pattern reflected by the presence of vascular invasion (VI) or extrahepatic spread (EHS). This study aimed to derive a more relevant staging system by modification of the BCLC system considering the prognostic implication of PS.
METHODS: A total of 7,501 subjects who were registered in the Korean multicenter hepatocellular carcinoma (HCC) registry database from 2008 to 2013 were analyzed. The relative goodness-of-fit between staging systems was compared using the Akaike information criterion (AIC) and integrated area under the curve (IAUC). Three modified BCLC (m-BCLC) systems (#1, #2, and #3) were devised by reducing the role of PS.
RESULTS: As a result, the BCLC C stage, which includes patients with PS 1-2 without VI/EHS, was reassigned to stage 0, A, or B according to their tumor burden in the m-BCLC #2 model. This model was identified as the most explanatory and desirable model for HCC staging by demonstrating the smallest AIC (AIC=70,088.01) and the largest IAUC (IAUC=0.722), while the original BCLC showed the largest AIC (AIC=70,697.17) and the smallest IAUC (IAUC=0.705). The m-BCLC #2 stage C was further subclassified into C1, C2, C3, and C4 according to the Child-Pugh score, PS, presence of EHS, and tumor extent. The C1 to C4 subgroups showed significantly different overall survival distribution between groups (p<0.001).
CONCLUSIONS: An accurate and relevant staging system for patients with HCC was derived though modification of the BCLC system based on PS.
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dc.language.isoen-
dc.subject.MESHCarcinoma, Hepatocellular-
dc.subject.MESHFemale-
dc.subject.MESHHepatitis B, Chronic-
dc.subject.MESHHepatitis C, Chronic-
dc.subject.MESHHumans-
dc.subject.MESHLiver Neoplasms-
dc.subject.MESHMale-
dc.subject.MESHMiddle Aged-
dc.subject.MESHNeoplasm Staging-
dc.subject.MESHPrognosis-
dc.subject.MESHRegistries-
dc.subject.MESHRepublic of Korea-
dc.subject.MESHSurvival Analysis-
dc.subject.MESHTumor Burden-
dc.titleA Proposal for Modification of the Barcelona Clinic Liver Cancer Staging System Considering the Prognostic Implication of Performance Status-
dc.typeArticle-
dc.identifier.pmid31023007-
dc.identifier.urlhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC6743810/-
dc.subject.keywordBarcelona Clinic Liver Cancer Staging-
dc.subject.keywordEastern Cooperative Oncology Group performance status-
dc.subject.keywordHepatocellular carcinoma-
dc.subject.keywordStage-
dc.contributor.affiliatedAuthor조, 효정-
dc.contributor.affiliatedAuthor김, 순선-
dc.contributor.affiliatedAuthor양, 민재-
dc.contributor.affiliatedAuthor노, 충균-
dc.contributor.affiliatedAuthor황, 재철-
dc.contributor.affiliatedAuthor임, 선교-
dc.contributor.affiliatedAuthor신, 성재-
dc.contributor.affiliatedAuthor이, 기명-
dc.contributor.affiliatedAuthor유, 병무-
dc.contributor.affiliatedAuthor이, 광재-
dc.contributor.affiliatedAuthor김, 진홍-
dc.contributor.affiliatedAuthor정, 재연-
dc.type.localJournal Papers-
dc.identifier.doi10.5009/gnl18444-
dc.citation.titleGut and liver-
dc.citation.volume13-
dc.citation.number5-
dc.citation.date2019-
dc.citation.startPage557-
dc.citation.endPage568-
dc.identifier.bibliographicCitationGut and liver, 13(5). : 557-568, 2019-
dc.identifier.eissn2005-1212-
dc.relation.journalidJ019762283-
Appears in Collections:
Journal Papers > School of Medicine / Graduate School of Medicine > Gastroenterology
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