Tumor and liver determinants of prognosis in unresectable hepatocellular carcinoma: A case cohort study

Background and Aims:  A total of 967 patients with unresectable and untransplantable, biopsy‐proven hepatocellular carcinoma (HCC) were prospectively evaluated at baseline and followed up till death. Methods:  Survival was the end‐point for all analyses. Results:  We found in our overall analysis, t...

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Published inJournal of gastroenterology and hepatology Vol. 23; no. 8pt1; pp. 1259 - 1266
Main Authors Carr, Brian I, Buch, Shama C, Kondragunta, Venkateswarlu, Pancoska, Petr, Branch, Robert A
Format Journal Article
LanguageEnglish
Published Melbourne, Australia Blackwell Publishing Asia 01.08.2008
Blackwell Science
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Summary:Background and Aims:  A total of 967 patients with unresectable and untransplantable, biopsy‐proven hepatocellular carcinoma (HCC) were prospectively evaluated at baseline and followed up till death. Methods:  Survival was the end‐point for all analyses. Results:  We found in our overall analysis, that male gender, ascites, cirrhosis, portal vein thrombosis (PVT), elevated alpha‐fetoprotein (AFP) or bilirubin or alkaline phosphatases were each statistically significant adverse prognostic factors. Patients with normal AFP survived longer than those with elevated AFP, in the presence of PVT, large or bilobar tumors or cirrhosis. We used a bivariate analysis to separate patient subgroups based on poor liver function and aggressive tumor characteristics. In subgroup analysis based on these subsets, there was clear discrimination in survival between subsets; in addition both cirrhosis and presence of PVT were significant, independent but modest risk factors. The results of this large dataset show that amongst nonsurgical HCC patients, there are clear subsets with longer survival than other subsets. Conclusions:  This data also supports the concept of heterogeneity of HCC.
Bibliography:istex:3749C184FE8705D277B97DCD24FE05B48AC6D4EA
ArticleID:JGH5487
ark:/67375/WNG-90891D3K-C
ObjectType-Article-1
SourceType-Scholarly Journals-1
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content type line 23
ISSN:0815-9319
1440-1746
DOI:10.1111/j.1440-1746.2008.05487.x