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Liver transplant for large hepatocellular carcinoma in Malatya: The role of gamma glutamyl transferase and alpha-fetoprotein, a retrospective cohort study

BACKGROUND: There is increasing interest in transplanting patients with hepatocellular carcinoma (HCC) with tumors greater than 5 cm (Milan criteria).  AIM: To investigate possible prognostically-useful factors for liver transplantation in HCC patients with large tumors. METHODS: In this clinical st...

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Autores principales: Ince, Volkan, Carr, Brian I, Bag, Harika Gozukara, Ersan, Veysel, Usta, Sertac, Koc, Cemalettin, Gonultas, Fatih, Sarici, Baris Kemal, Karakas, Serdar, Kutluturk, Koray, Baskiran, Adil, Yilmaz, Sezai
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Baishideng Publishing Group Inc 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7769743/
https://www.ncbi.nlm.nih.gov/pubmed/33437403
http://dx.doi.org/10.4240/wjgs.v12.i12.520
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author Ince, Volkan
Carr, Brian I
Bag, Harika Gozukara
Ersan, Veysel
Usta, Sertac
Koc, Cemalettin
Gonultas, Fatih
Sarici, Baris Kemal
Karakas, Serdar
Kutluturk, Koray
Baskiran, Adil
Yilmaz, Sezai
author_facet Ince, Volkan
Carr, Brian I
Bag, Harika Gozukara
Ersan, Veysel
Usta, Sertac
Koc, Cemalettin
Gonultas, Fatih
Sarici, Baris Kemal
Karakas, Serdar
Kutluturk, Koray
Baskiran, Adil
Yilmaz, Sezai
author_sort Ince, Volkan
collection PubMed
description BACKGROUND: There is increasing interest in transplanting patients with hepatocellular carcinoma (HCC) with tumors greater than 5 cm (Milan criteria).  AIM: To investigate possible prognostically-useful factors for liver transplantation in HCC patients with large tumors. METHODS: In this clinical study, 50 patients with HCC who were transplanted at our Liver Transplant Center between April 2006 and August 2019 and had tumors greater than 6 cm maximum diameter were retrospectively analyzed. Their survival and full clinical characteristics were examined, with respect to serum alpha-fetoprotein (AFP) and gamma glutamyl transpeptidase (GGT) levels. Kaplan-Meier survival estimates were used to determine overall survival and disease-free survival in these patients. The inclusion criterion was evidence of HCC. Exclusion criteria were the presence of macroscopic portal vein thrombosis or metastasis and a follow-up period of less than 90 d. RESULTS: Using receiver operating characteristic curve (ROC) analysis, cutoff values of AFP 200 ng/mL and GGT 104 IU/L were identified and used in this study. Significantly longer overall survival (OS) and disease-free-survival (DFS) were found in patients who had lower values of either parameter, compared with higher values.  Even greater differences in survival were found when the 2 parameters were combined. Two tumor size bands were identified, in searching for the limits of this approach with larger tumors, namely 6-10 cm and > 10 cm. Combination parameters in the 6-10 cm band reflected 5-year OS of 76.2% in patients with low AFP plus low GGT vs 0% for all other groups. Patients with tumors greater than 10 cm, did not have low AFP plus low GGT. The most consistent clinical correlates for longer survival were degree of tumor differentiation and absence of microscopic portal venous invasion. CONCLUSION: Serum levels of AFP and GGT, both alone and combined, represent a simple prognostic identifier in patients with large HCCs undergoing liver transplant-ation.
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spelling pubmed-77697432021-01-11 Liver transplant for large hepatocellular carcinoma in Malatya: The role of gamma glutamyl transferase and alpha-fetoprotein, a retrospective cohort study Ince, Volkan Carr, Brian I Bag, Harika Gozukara Ersan, Veysel Usta, Sertac Koc, Cemalettin Gonultas, Fatih Sarici, Baris Kemal Karakas, Serdar Kutluturk, Koray Baskiran, Adil Yilmaz, Sezai World J Gastrointest Surg Clinical Trials Study BACKGROUND: There is increasing interest in transplanting patients with hepatocellular carcinoma (HCC) with tumors greater than 5 cm (Milan criteria).  AIM: To investigate possible prognostically-useful factors for liver transplantation in HCC patients with large tumors. METHODS: In this clinical study, 50 patients with HCC who were transplanted at our Liver Transplant Center between April 2006 and August 2019 and had tumors greater than 6 cm maximum diameter were retrospectively analyzed. Their survival and full clinical characteristics were examined, with respect to serum alpha-fetoprotein (AFP) and gamma glutamyl transpeptidase (GGT) levels. Kaplan-Meier survival estimates were used to determine overall survival and disease-free survival in these patients. The inclusion criterion was evidence of HCC. Exclusion criteria were the presence of macroscopic portal vein thrombosis or metastasis and a follow-up period of less than 90 d. RESULTS: Using receiver operating characteristic curve (ROC) analysis, cutoff values of AFP 200 ng/mL and GGT 104 IU/L were identified and used in this study. Significantly longer overall survival (OS) and disease-free-survival (DFS) were found in patients who had lower values of either parameter, compared with higher values.  Even greater differences in survival were found when the 2 parameters were combined. Two tumor size bands were identified, in searching for the limits of this approach with larger tumors, namely 6-10 cm and > 10 cm. Combination parameters in the 6-10 cm band reflected 5-year OS of 76.2% in patients with low AFP plus low GGT vs 0% for all other groups. Patients with tumors greater than 10 cm, did not have low AFP plus low GGT. The most consistent clinical correlates for longer survival were degree of tumor differentiation and absence of microscopic portal venous invasion. CONCLUSION: Serum levels of AFP and GGT, both alone and combined, represent a simple prognostic identifier in patients with large HCCs undergoing liver transplant-ation. Baishideng Publishing Group Inc 2020-12-27 2020-12-27 /pmc/articles/PMC7769743/ /pubmed/33437403 http://dx.doi.org/10.4240/wjgs.v12.i12.520 Text en ©The Author(s) 2020. Published by Baishideng Publishing Group Inc. All rights reserved. http://creativecommons.org/licenses/by-nc/4.0/ This article is an open-access article that was selected by an in-house editor and fully peer-reviewed by external reviewers. It is distributed in accordance with the Creative Commons Attribution NonCommercial (CC BY-NC 4.0) license, which permits others to distribute, remix, adapt, build upon this work non-commercially, and license their derivative works on different terms, provided the original work is properly cited and the use is non-commercial. See: http://creativecommons.org/Licenses/by-nc/4.0/
spellingShingle Clinical Trials Study
Ince, Volkan
Carr, Brian I
Bag, Harika Gozukara
Ersan, Veysel
Usta, Sertac
Koc, Cemalettin
Gonultas, Fatih
Sarici, Baris Kemal
Karakas, Serdar
Kutluturk, Koray
Baskiran, Adil
Yilmaz, Sezai
Liver transplant for large hepatocellular carcinoma in Malatya: The role of gamma glutamyl transferase and alpha-fetoprotein, a retrospective cohort study
title Liver transplant for large hepatocellular carcinoma in Malatya: The role of gamma glutamyl transferase and alpha-fetoprotein, a retrospective cohort study
title_full Liver transplant for large hepatocellular carcinoma in Malatya: The role of gamma glutamyl transferase and alpha-fetoprotein, a retrospective cohort study
title_fullStr Liver transplant for large hepatocellular carcinoma in Malatya: The role of gamma glutamyl transferase and alpha-fetoprotein, a retrospective cohort study
title_full_unstemmed Liver transplant for large hepatocellular carcinoma in Malatya: The role of gamma glutamyl transferase and alpha-fetoprotein, a retrospective cohort study
title_short Liver transplant for large hepatocellular carcinoma in Malatya: The role of gamma glutamyl transferase and alpha-fetoprotein, a retrospective cohort study
title_sort liver transplant for large hepatocellular carcinoma in malatya: the role of gamma glutamyl transferase and alpha-fetoprotein, a retrospective cohort study
topic Clinical Trials Study
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7769743/
https://www.ncbi.nlm.nih.gov/pubmed/33437403
http://dx.doi.org/10.4240/wjgs.v12.i12.520
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