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 in | Journal of gastroenterology and hepatology Vol. 23; no. 8pt1; pp. 1259 - 1266 |
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Main Authors | , , , , |
Format | Journal Article |
Language | English |
Published |
Melbourne, Australia
Blackwell Publishing Asia
01.08.2008
Blackwell Science |
Subjects | |
Online Access | Get full text |
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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. |
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Bibliography: | istex:3749C184FE8705D277B97DCD24FE05B48AC6D4EA ArticleID:JGH5487 ark:/67375/WNG-90891D3K-C ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 23 |
ISSN: | 0815-9319 1440-1746 |
DOI: | 10.1111/j.1440-1746.2008.05487.x |