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Hepatitis B vs. hepatitis C infection on viral hepatitis-associated hepatocellular carcinoma
BACKGROUND: To determine clinical-pathologic variables in patients with a new diagnosis of hepatocellular carcinoma (HCC) and underlying hepatitis B vs. C infection. METHODS: Patients presenting to a single urban hospital with a new diagnosis of HCC were entered into a clinical database. Variables i...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2012
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3407024/ https://www.ncbi.nlm.nih.gov/pubmed/22681852 http://dx.doi.org/10.1186/1471-230X-12-64 |
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author | Hiotis, Spiros P Rahbari, Nuh N Villanueva, Gerald A Klegar, Eunjie Luan, Wei Wang, Qin Yee, Herman T |
author_facet | Hiotis, Spiros P Rahbari, Nuh N Villanueva, Gerald A Klegar, Eunjie Luan, Wei Wang, Qin Yee, Herman T |
author_sort | Hiotis, Spiros P |
collection | PubMed |
description | BACKGROUND: To determine clinical-pathologic variables in patients with a new diagnosis of hepatocellular carcinoma (HCC) and underlying hepatitis B vs. C infection. METHODS: Patients presenting to a single urban hospital with a new diagnosis of HCC were entered into a clinical database. Variables including number and size of tumors, presence of metastases, serum alpha-Fetoprotein, hepatitis serologies, severity of hepatic dysfunction, and presence of cirrhosis were evaluated in 127 patients. RESULTS: Patients with hepatitis B (HBV) were more likely to develop HCC at a younger age than patients with hepatitis C (HCV) (HBV-26% under age 40, HCV-0% under age 40; p < 0.001), with greater serum alpha-Fetoprotein production (median level: HBV-1000 ng/ml vs. HCV-37 ng/ml; p = 0.002), with larger tumors (HBV-78% >5 cm, HCV-28% >5 cm; p < 0.001), in the absence of cirrhosis (HBV-40%, HCV-0%; p < 0.001), and a decreased eligibility for curative treatment (HBV-14%, HCV-34%; p < 0.05). Conversely, patients with HCV were more likely to develop HCC in association with multiple co-morbidities, cirrhosis, and older age. CONCLUSIONS: Significant clinical-pathologic differences exist among HCC patients with underlying HBV vs. HCV. These differences impact eligibility for potentially-curative therapy and prognosis. |
format | Online Article Text |
id | pubmed-3407024 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2012 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-34070242012-07-28 Hepatitis B vs. hepatitis C infection on viral hepatitis-associated hepatocellular carcinoma Hiotis, Spiros P Rahbari, Nuh N Villanueva, Gerald A Klegar, Eunjie Luan, Wei Wang, Qin Yee, Herman T BMC Gastroenterol Research Article BACKGROUND: To determine clinical-pathologic variables in patients with a new diagnosis of hepatocellular carcinoma (HCC) and underlying hepatitis B vs. C infection. METHODS: Patients presenting to a single urban hospital with a new diagnosis of HCC were entered into a clinical database. Variables including number and size of tumors, presence of metastases, serum alpha-Fetoprotein, hepatitis serologies, severity of hepatic dysfunction, and presence of cirrhosis were evaluated in 127 patients. RESULTS: Patients with hepatitis B (HBV) were more likely to develop HCC at a younger age than patients with hepatitis C (HCV) (HBV-26% under age 40, HCV-0% under age 40; p < 0.001), with greater serum alpha-Fetoprotein production (median level: HBV-1000 ng/ml vs. HCV-37 ng/ml; p = 0.002), with larger tumors (HBV-78% >5 cm, HCV-28% >5 cm; p < 0.001), in the absence of cirrhosis (HBV-40%, HCV-0%; p < 0.001), and a decreased eligibility for curative treatment (HBV-14%, HCV-34%; p < 0.05). Conversely, patients with HCV were more likely to develop HCC in association with multiple co-morbidities, cirrhosis, and older age. CONCLUSIONS: Significant clinical-pathologic differences exist among HCC patients with underlying HBV vs. HCV. These differences impact eligibility for potentially-curative therapy and prognosis. BioMed Central 2012-06-08 /pmc/articles/PMC3407024/ /pubmed/22681852 http://dx.doi.org/10.1186/1471-230X-12-64 Text en Copyright ©2012 Hiotis et al.; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Article Hiotis, Spiros P Rahbari, Nuh N Villanueva, Gerald A Klegar, Eunjie Luan, Wei Wang, Qin Yee, Herman T Hepatitis B vs. hepatitis C infection on viral hepatitis-associated hepatocellular carcinoma |
title | Hepatitis B vs. hepatitis C infection on viral hepatitis-associated hepatocellular carcinoma |
title_full | Hepatitis B vs. hepatitis C infection on viral hepatitis-associated hepatocellular carcinoma |
title_fullStr | Hepatitis B vs. hepatitis C infection on viral hepatitis-associated hepatocellular carcinoma |
title_full_unstemmed | Hepatitis B vs. hepatitis C infection on viral hepatitis-associated hepatocellular carcinoma |
title_short | Hepatitis B vs. hepatitis C infection on viral hepatitis-associated hepatocellular carcinoma |
title_sort | hepatitis b vs. hepatitis c infection on viral hepatitis-associated hepatocellular carcinoma |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3407024/ https://www.ncbi.nlm.nih.gov/pubmed/22681852 http://dx.doi.org/10.1186/1471-230X-12-64 |
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