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Tenofovir versus entecavir on the prognosis of hepatitis B-related hepatocellular carcinoma after surgical resection: a randomised controlled trial
BACKGROUND: Nucleot(s)ide analog treatment (entecavir (ETV) and tenofovir (TDF)) is reported to be associated with decreased tumor recurrence and death in hepatitis B virus (HBV)-related hepatocellular carcinoma (HCC) patients, yet further work is needed to evaluate the different efficacies of these...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Lippincott Williams & Wilkins
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10583900/ https://www.ncbi.nlm.nih.gov/pubmed/37335984 http://dx.doi.org/10.1097/JS9.0000000000000554 |
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author | Linye, He Zijing, Xia Xiaoyun, Zhang Zhihui, Li Tianfu, Wen Chuan, Li |
author_facet | Linye, He Zijing, Xia Xiaoyun, Zhang Zhihui, Li Tianfu, Wen Chuan, Li |
author_sort | Linye, He |
collection | PubMed |
description | BACKGROUND: Nucleot(s)ide analog treatment (entecavir (ETV) and tenofovir (TDF)) is reported to be associated with decreased tumor recurrence and death in hepatitis B virus (HBV)-related hepatocellular carcinoma (HCC) patients, yet further work is needed to evaluate the different efficacies of these two agents on the prognosis of early-stage HBV-related HCC patients after curative liver resection. MATERIAL AND METHODS: From July 2017 to January 2019, 148 patients with HBV-related HCC who underwent curative liver resection were randomized to receive TDF (n=74) or ETV (n=74) therapy. The primary end point was tumor recurrence in the intention-to-treat population. Overall survival and tumor recurrence of patients were compared by multivariable-adjusted Cox regression and competing risk analyses. RESULTS: During the follow-up with continued antiviral therapy, 37 (25.0%) patients developed tumor recurrence, and 16 (10.8%) patients died (N=15) or received liver transplantation (N=1). In the intention-to-treat cohort, the recurrence-free survival for the TDF group was significantly better than that for the ETV group (P=0.026). In the multivariate analysis, the relative risks of recurrence and death/liver transplantation for ETV therapy were 3.056 (95% CI: 1.015–9.196; P=0.047) and 2.566 (95% CI: 1.264–5.228; P=0.009), respectively. Subgroup analysis of the PP population indicated a better overall survival and RFS of patients receiving TDF therapy (P=0.048; hazard ratio (HR) =0.362; 95% CI: 0.132–0.993 and P=0.014; HR =0.458; 95% CI: 0.245–0.856). Additionally, TDF therapy was an independent protective factor against late tumor recurrence (P=0.046; (HR)=0.432; 95% CI: 0.189–0.985) but not against early tumor recurrence (P=0.109; HR =1.964; 95% CI: 0.858–4.494). CONCLUSION: HBV-related HCC patients treated with consistent TDF therapy had a significantly lower risk of tumor recurrence than those treated with ETV after curative treatment. |
format | Online Article Text |
id | pubmed-10583900 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Lippincott Williams & Wilkins |
record_format | MEDLINE/PubMed |
spelling | pubmed-105839002023-10-19 Tenofovir versus entecavir on the prognosis of hepatitis B-related hepatocellular carcinoma after surgical resection: a randomised controlled trial Linye, He Zijing, Xia Xiaoyun, Zhang Zhihui, Li Tianfu, Wen Chuan, Li Int J Surg Original Research BACKGROUND: Nucleot(s)ide analog treatment (entecavir (ETV) and tenofovir (TDF)) is reported to be associated with decreased tumor recurrence and death in hepatitis B virus (HBV)-related hepatocellular carcinoma (HCC) patients, yet further work is needed to evaluate the different efficacies of these two agents on the prognosis of early-stage HBV-related HCC patients after curative liver resection. MATERIAL AND METHODS: From July 2017 to January 2019, 148 patients with HBV-related HCC who underwent curative liver resection were randomized to receive TDF (n=74) or ETV (n=74) therapy. The primary end point was tumor recurrence in the intention-to-treat population. Overall survival and tumor recurrence of patients were compared by multivariable-adjusted Cox regression and competing risk analyses. RESULTS: During the follow-up with continued antiviral therapy, 37 (25.0%) patients developed tumor recurrence, and 16 (10.8%) patients died (N=15) or received liver transplantation (N=1). In the intention-to-treat cohort, the recurrence-free survival for the TDF group was significantly better than that for the ETV group (P=0.026). In the multivariate analysis, the relative risks of recurrence and death/liver transplantation for ETV therapy were 3.056 (95% CI: 1.015–9.196; P=0.047) and 2.566 (95% CI: 1.264–5.228; P=0.009), respectively. Subgroup analysis of the PP population indicated a better overall survival and RFS of patients receiving TDF therapy (P=0.048; hazard ratio (HR) =0.362; 95% CI: 0.132–0.993 and P=0.014; HR =0.458; 95% CI: 0.245–0.856). Additionally, TDF therapy was an independent protective factor against late tumor recurrence (P=0.046; (HR)=0.432; 95% CI: 0.189–0.985) but not against early tumor recurrence (P=0.109; HR =1.964; 95% CI: 0.858–4.494). CONCLUSION: HBV-related HCC patients treated with consistent TDF therapy had a significantly lower risk of tumor recurrence than those treated with ETV after curative treatment. Lippincott Williams & Wilkins 2023-06-16 /pmc/articles/PMC10583900/ /pubmed/37335984 http://dx.doi.org/10.1097/JS9.0000000000000554 Text en Copyright © 2023 The Author(s). Published by Wolters Kluwer Health, Inc. https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article distributed under the terms of the Creative Commons Attribution-Non Commercial-No Derivatives License 4.0 (https://creativecommons.org/licenses/by-nc-nd/4.0/) (CCBY-NC-ND), where it is permissible to download and share the work provided it is properly cited. The work cannot be changed in any way or used commercially without permission from the journal. http://creativecommons.org/licenses/by-nc-nd/4.0/ (https://creativecommons.org/licenses/by-nc-nd/4.0/) |
spellingShingle | Original Research Linye, He Zijing, Xia Xiaoyun, Zhang Zhihui, Li Tianfu, Wen Chuan, Li Tenofovir versus entecavir on the prognosis of hepatitis B-related hepatocellular carcinoma after surgical resection: a randomised controlled trial |
title | Tenofovir versus entecavir on the prognosis of hepatitis B-related hepatocellular carcinoma after surgical resection: a randomised controlled trial |
title_full | Tenofovir versus entecavir on the prognosis of hepatitis B-related hepatocellular carcinoma after surgical resection: a randomised controlled trial |
title_fullStr | Tenofovir versus entecavir on the prognosis of hepatitis B-related hepatocellular carcinoma after surgical resection: a randomised controlled trial |
title_full_unstemmed | Tenofovir versus entecavir on the prognosis of hepatitis B-related hepatocellular carcinoma after surgical resection: a randomised controlled trial |
title_short | Tenofovir versus entecavir on the prognosis of hepatitis B-related hepatocellular carcinoma after surgical resection: a randomised controlled trial |
title_sort | tenofovir versus entecavir on the prognosis of hepatitis b-related hepatocellular carcinoma after surgical resection: a randomised controlled trial |
topic | Original Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10583900/ https://www.ncbi.nlm.nih.gov/pubmed/37335984 http://dx.doi.org/10.1097/JS9.0000000000000554 |
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