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dc.contributor.authorKawashima, J.-
dc.contributor.authorAkabane, M.-
dc.contributor.authorKhalil, M.-
dc.contributor.authorWoldesenbet, S.-
dc.contributor.authorEndo, Y.-
dc.contributor.authorSahara, K.-
dc.contributor.authorRuzzenente, A.-
dc.contributor.authorRatti, F.-
dc.contributor.authorMarques, H. P.-
dc.contributor.authorOliveira, S.-
dc.contributor.authorBalaia, J.-
dc.contributor.authorCauchy, F.-
dc.contributor.authorLam, Vincent W. T.-
dc.contributor.authorPoultsides, G. A.-
dc.contributor.authorKitago, M.-
dc.contributor.authorPopescu, I.-
dc.contributor.authorMartel, G.-
dc.contributor.authorGleisner, A.-
dc.contributor.authorHugh, T.-
dc.contributor.authorWeiss, M.-
dc.contributor.authorAucejo, F.-
dc.contributor.authorAldrighetti, L.-
dc.contributor.authorEndo, I.-
dc.contributor.authorPawlik, T. M.-
dc.date.accessioned2025-06-02T02:16:06Z-
dc.date.available2025-06-02T02:16:06Z-
dc.date.issued2025-
dc.identifier.citationSurgery. 183:109388, 2025 Jul-
dc.identifier.urihttps://wslhd.intersearch.com.au/wslhdjspui/handle/1/11039-
dc.description.abstractINTRODUCTION: Morphologic criteria, such as the Barcelona Clinic Liver Cancer staging system often fail to accurately predict long-term survival among patients undergoing liver resection for hepatocellular carcinoma. We sought to develop a continuous risk score that incorporates established markers of tumor biology and liver function to improve the prediction of overall survival. METHODS: Data from a multi-institutional database were used to identify patients who underwent curative-intent hepatectomy for hepatocellular carcinoma. A predictive score for overall survival was developed using weighted beta-coefficients from a multivariable Cox regression model. RESULTS: Among 850 patients, 595 (70.0%) were assigned to the training cohort, and 255 (30.0%) to the test cohort. In the training cohort, multivariable analysis identified the Model of End-Stage Liver Disease (hazard ratio, 1.04; 95% confidence interval, 1.01-1.07), log-transformed alpha-fetoprotein (hazard ratio, 1.07; 95% confidence interval, 1.02-1.13), and tumor burden score (hazard ratio, 1.07; 95% confidence interval, 1.03-1.11) as independent predictors of worse overall survival. The Model of End-Stage Liver Disease-alpha-fetoprotein-tumor burden score, based on the Cox model, stratified patients into low-risk (n = 466, 78.3%) with a 5-year OS of 70.5% and high-risk (n = 129, 21.7%) with a 5-year OS of 47.0% (P < .001). In the test cohort, the Model of End-Stage Liver Disease-alpha-fetoprotein-tumor burden score demonstrated superior discriminative accuracy (C-index: 0.72, time-dependent area under the curve 1-year: 0.80, 3-year 0.76, 5-year 0.70) compared with the Barcelona Clinic Liver Cancer staging system (C-index: 0.53, time-dependent area under the curve 1-year: 0.61, 3-year 0.55, 5-year 0.56). An online tool was made accessible at https://jk-osu.shinyapps.io/MELD_AFP_TBS/. CONCLUSIONS: The Model of End-Stage Liver Disease-alpha-fetoprotein-tumor burden score provides a novel, accurate tool for prognostic stratification of patients with hepatocellular carcinoma, identifying high-risk patients who may benefit from alternative treatments to improve outcomes.-
dc.subjectHepatology-
dc.subjectSurgery-
dc.subjectOncology-
dc.titleModel of End-Stage Liver Disease-alpha-fetoprotein-tumor burden (MELD-AFP-TBS) score to stratify prognosis after liver resection for hepatocellular carcinoma-
dc.typeJournal Article-
dc.identifier.doihttps://doi.org/10.1016/j.surg.2025.109388-
dc.subject.keywordsdrug therapy-
dc.subject.keywordsend stage liver disease-
dc.subject.keywordshepatectomy-
dc.subject.keywordsliver cell carcinoma-
dc.subject.keywordsliver function-
dc.subject.keywordslong term survival-
dc.subject.keywordstumor burden-
dc.subject.keywordsalpha fetoprotein-
dc.identifier.journaltitleSurgery-
dc.identifier.departmentSurgery-
dc.contributor.wslhdLam, Vincent W. T.-
dc.type.studyortrialCohort Analysis-
dc.type.studyortrialMajor Clinical Study-
dc.identifier.pmid40311416-
dc.identifier.affiliationDepartment of Surgery, The Ohio State University Wexner Medical Center and James Comprehensive Cancer Center, Columbus, OH, United States-
dc.identifier.affiliationDepartment of Gastroenterological Surgery, Yokohama City University, Yokohama, Japan-
dc.identifier.affiliationDepartment of Transplant Surgery, University of Rochester Medical Center, Rochester, NY, United States-
dc.identifier.affiliationDivision of General and Hepatobiliary Surgery, University of Verona, Verona, Italy-
dc.identifier.affiliationDepartment of Surgery, San Raffaele Hospital, Milan, Italy-
dc.identifier.affiliationDepartment of Surgery, Curry Cabral Hospital, Lisbon, Portugal-
dc.identifier.affiliationDepartment of HPB Surgery and Liver Transplantation, Beaujon Hospital, Clichy, France-
dc.identifier.affiliationDepartment of Surgery, Westmead Hospital, Westmead, NSW, Australia-
dc.identifier.affiliationDepartment of Surgery, Stanford University, Stanford, CA, United States-
dc.identifier.affiliationDepartment of Surgery, Keio University, Tokyo, Japan-
dc.identifier.affiliationDepartment of Surgery, Fundeni Clinical Institute, Bucharest, Romania-
dc.identifier.affiliationDepartment of Surgery, University of Ottawa, Ottawa, ON, Canada-
dc.identifier.affiliationDepartment of Surgery, University of Colorado Denver, Denver, CO, United States-
dc.identifier.affiliationDepartment of Surgery, The University of Sydney, Sydney, NSW, Australia-
dc.identifier.affiliationDepartment of Surgery, Cancer Institute, Northwell Health, New Hyde Park, NY, United States-
dc.identifier.affiliationDepartment of Hepato-pancreato-biliary & Liver Transplant Surgery, Cleveland Clinic Foundation, Digestive Diseases and Surgery Institute, Cleveland, OH, United States-
dc.identifier.facilityWestmead-
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