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Effect of Heavy Alcohol Intake on Long‐term Results after Curative Resection of Hepatitis C Virus‐related Hepatocellular Carcinoma

We studied the effect of heavy alcohol intake (ethanol intake ≥80 g/day for ≥5 yr) on long‐term results in 53 patients with hepatitis C virus (HCV)‐related hepatocellular carcinoma (HCC) who had undergone curative hepatic resection. Cell proliferative activity in the tumor and non‐tumorous liver was...

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Autores principales: Okada, Shuichi, Ishii, Hiroshi, Nose, Haruhiko, Okusaka, Takuji, Kyogoku, Akiko, Yoshimori, Masayoshi, Shimada, Kazuaki, Yamamoto, Junji, Kosuge, Tomoo, Yamasaki, Susumu, Sakamoto, Michiie, Hirohashi, Setsuo
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Blackwell Publishing Ltd 1996
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5921169/
https://www.ncbi.nlm.nih.gov/pubmed/8797895
http://dx.doi.org/10.1111/j.1349-7006.1996.tb02113.x
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author Okada, Shuichi
Ishii, Hiroshi
Nose, Haruhiko
Okusaka, Takuji
Kyogoku, Akiko
Yoshimori, Masayoshi
Shimada, Kazuaki
Yamamoto, Junji
Kosuge, Tomoo
Yamasaki, Susumu
Sakamoto, Michiie
Hirohashi, Setsuo
author_facet Okada, Shuichi
Ishii, Hiroshi
Nose, Haruhiko
Okusaka, Takuji
Kyogoku, Akiko
Yoshimori, Masayoshi
Shimada, Kazuaki
Yamamoto, Junji
Kosuge, Tomoo
Yamasaki, Susumu
Sakamoto, Michiie
Hirohashi, Setsuo
author_sort Okada, Shuichi
collection PubMed
description We studied the effect of heavy alcohol intake (ethanol intake ≥80 g/day for ≥5 yr) on long‐term results in 53 patients with hepatitis C virus (HCV)‐related hepatocellular carcinoma (HCC) who had undergone curative hepatic resection. Cell proliferative activity in the tumor and non‐tumorous liver was also assessed by counting argyrophilic nucleolar organizer region‐associated proteins (Ag‐NOR) in the resected specimens. Twenty patients (20 males, 0 females) were positive for heavy alcohol intake [AI(+)] and 33 (28 males, 5 females) were not [AI(‐)]. All patients were positive for HCV antibody and negative for hepatitis B surface antigen. Carcinoma recurred within 3 to 51 postoperative months in 42 (79.2%) of the 53 patients. The median disease‐free survival time was 12.6 mo in the AI(+) group and 25.4 mo in the AI(‐) group (P<0.01). The AI(+) group also had significantly poorer survival than the AI(‐) group (P<0.05, 3‐year survival rate: 66.7% vs. 93.5%). HCC tumor in the AI(+) group showed significantly increased proliferative activity compared with that in the AI(‐) group (P<0.05, Ag‐NOR number: 2.3±0.8 vs. 1.9±0.4). However, there was no significant difference between the numbers of Ag‐NORs in non‐tumorous liver from these two groups (1.5±0.2 vs. 1.5±0.2). Patients with heavy alcohol intake should be followed particularly closely, even if they have received curative surgery, since heavy alcohol intake is closely related to a poor postoperative prognosis.
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spelling pubmed-59211692018-05-11 Effect of Heavy Alcohol Intake on Long‐term Results after Curative Resection of Hepatitis C Virus‐related Hepatocellular Carcinoma Okada, Shuichi Ishii, Hiroshi Nose, Haruhiko Okusaka, Takuji Kyogoku, Akiko Yoshimori, Masayoshi Shimada, Kazuaki Yamamoto, Junji Kosuge, Tomoo Yamasaki, Susumu Sakamoto, Michiie Hirohashi, Setsuo Jpn J Cancer Res Article We studied the effect of heavy alcohol intake (ethanol intake ≥80 g/day for ≥5 yr) on long‐term results in 53 patients with hepatitis C virus (HCV)‐related hepatocellular carcinoma (HCC) who had undergone curative hepatic resection. Cell proliferative activity in the tumor and non‐tumorous liver was also assessed by counting argyrophilic nucleolar organizer region‐associated proteins (Ag‐NOR) in the resected specimens. Twenty patients (20 males, 0 females) were positive for heavy alcohol intake [AI(+)] and 33 (28 males, 5 females) were not [AI(‐)]. All patients were positive for HCV antibody and negative for hepatitis B surface antigen. Carcinoma recurred within 3 to 51 postoperative months in 42 (79.2%) of the 53 patients. The median disease‐free survival time was 12.6 mo in the AI(+) group and 25.4 mo in the AI(‐) group (P<0.01). The AI(+) group also had significantly poorer survival than the AI(‐) group (P<0.05, 3‐year survival rate: 66.7% vs. 93.5%). HCC tumor in the AI(+) group showed significantly increased proliferative activity compared with that in the AI(‐) group (P<0.05, Ag‐NOR number: 2.3±0.8 vs. 1.9±0.4). However, there was no significant difference between the numbers of Ag‐NORs in non‐tumorous liver from these two groups (1.5±0.2 vs. 1.5±0.2). Patients with heavy alcohol intake should be followed particularly closely, even if they have received curative surgery, since heavy alcohol intake is closely related to a poor postoperative prognosis. Blackwell Publishing Ltd 1996-08 /pmc/articles/PMC5921169/ /pubmed/8797895 http://dx.doi.org/10.1111/j.1349-7006.1996.tb02113.x Text en
spellingShingle Article
Okada, Shuichi
Ishii, Hiroshi
Nose, Haruhiko
Okusaka, Takuji
Kyogoku, Akiko
Yoshimori, Masayoshi
Shimada, Kazuaki
Yamamoto, Junji
Kosuge, Tomoo
Yamasaki, Susumu
Sakamoto, Michiie
Hirohashi, Setsuo
Effect of Heavy Alcohol Intake on Long‐term Results after Curative Resection of Hepatitis C Virus‐related Hepatocellular Carcinoma
title Effect of Heavy Alcohol Intake on Long‐term Results after Curative Resection of Hepatitis C Virus‐related Hepatocellular Carcinoma
title_full Effect of Heavy Alcohol Intake on Long‐term Results after Curative Resection of Hepatitis C Virus‐related Hepatocellular Carcinoma
title_fullStr Effect of Heavy Alcohol Intake on Long‐term Results after Curative Resection of Hepatitis C Virus‐related Hepatocellular Carcinoma
title_full_unstemmed Effect of Heavy Alcohol Intake on Long‐term Results after Curative Resection of Hepatitis C Virus‐related Hepatocellular Carcinoma
title_short Effect of Heavy Alcohol Intake on Long‐term Results after Curative Resection of Hepatitis C Virus‐related Hepatocellular Carcinoma
title_sort effect of heavy alcohol intake on long‐term results after curative resection of hepatitis c virus‐related hepatocellular carcinoma
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5921169/
https://www.ncbi.nlm.nih.gov/pubmed/8797895
http://dx.doi.org/10.1111/j.1349-7006.1996.tb02113.x
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