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Efficacy of Sorafenib for the Treatment of Post-Transplant Hepatocellular Carcinoma Recurrence
BACKGROUND: The role of sorafenib in patients with hepatocellular carcinoma (HCC) recurrence after liver transplantation (LT) has been rarely studied. The aim of this study was to evaluate the efficacy of sorafenib in post-LT era. METHODS: Consecutive patients with post-transplant HCC recurrence not...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
The Korean Academy of Medical Sciences
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6209769/ https://www.ncbi.nlm.nih.gov/pubmed/30402048 http://dx.doi.org/10.3346/jkms.2018.33.e283 |
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author | Kang, Seong Hee Cho, Hyeki Cho, Eun Ju Lee, Jeong-Hoon Yu, Su Jong Kim, Yoon Jun Yi, Nam-Joon Lee, Kwang-Woong Suh, Kyung-Suk Yoon, Jung-Hwan |
author_facet | Kang, Seong Hee Cho, Hyeki Cho, Eun Ju Lee, Jeong-Hoon Yu, Su Jong Kim, Yoon Jun Yi, Nam-Joon Lee, Kwang-Woong Suh, Kyung-Suk Yoon, Jung-Hwan |
author_sort | Kang, Seong Hee |
collection | PubMed |
description | BACKGROUND: The role of sorafenib in patients with hepatocellular carcinoma (HCC) recurrence after liver transplantation (LT) has been rarely studied. The aim of this study was to evaluate the efficacy of sorafenib in post-LT era. METHODS: Consecutive patients with post-transplant HCC recurrence not eligible to resection or locoregional therapy were included. Patients receiving best supportive care (BSC) until 2007 were compared with those treated by sorafenib thereafter. RESULTS: Of a total of 65 patients, 20 patients received BSC and 45 received sorafenib. Clinical characteristics were similar between two groups except that sorafenib group received tacrolimus and mammalian target-of-rapamycin inhibitors more frequently than BSC group. Treatment with sorafenib conferred a survival advantage as compared with BSC for survival after recurrence (median, 14.2 vs. 6.8 months; P = 0.01). In multivariate analyses, high serum α-fetoprotein level, synchronous intrahepatic recurrence and distant metastasis at the time of recurrence, and BSC were independently associated with poorer survival after recurrence. Sorafenib treatment was associated with better survival after recurrence as compared with BSC (hazard ratio, 0.25; 95% confidence interval, 0.10–0.62; P = 0.002). In addition, sorafenib group showed tolerable toxicity in the post-transplant setting. CONCLUSION: Sorafenib may be beneficial in patients with post-transplant HCC recurrence. |
format | Online Article Text |
id | pubmed-6209769 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | The Korean Academy of Medical Sciences |
record_format | MEDLINE/PubMed |
spelling | pubmed-62097692018-11-07 Efficacy of Sorafenib for the Treatment of Post-Transplant Hepatocellular Carcinoma Recurrence Kang, Seong Hee Cho, Hyeki Cho, Eun Ju Lee, Jeong-Hoon Yu, Su Jong Kim, Yoon Jun Yi, Nam-Joon Lee, Kwang-Woong Suh, Kyung-Suk Yoon, Jung-Hwan J Korean Med Sci Original Article BACKGROUND: The role of sorafenib in patients with hepatocellular carcinoma (HCC) recurrence after liver transplantation (LT) has been rarely studied. The aim of this study was to evaluate the efficacy of sorafenib in post-LT era. METHODS: Consecutive patients with post-transplant HCC recurrence not eligible to resection or locoregional therapy were included. Patients receiving best supportive care (BSC) until 2007 were compared with those treated by sorafenib thereafter. RESULTS: Of a total of 65 patients, 20 patients received BSC and 45 received sorafenib. Clinical characteristics were similar between two groups except that sorafenib group received tacrolimus and mammalian target-of-rapamycin inhibitors more frequently than BSC group. Treatment with sorafenib conferred a survival advantage as compared with BSC for survival after recurrence (median, 14.2 vs. 6.8 months; P = 0.01). In multivariate analyses, high serum α-fetoprotein level, synchronous intrahepatic recurrence and distant metastasis at the time of recurrence, and BSC were independently associated with poorer survival after recurrence. Sorafenib treatment was associated with better survival after recurrence as compared with BSC (hazard ratio, 0.25; 95% confidence interval, 0.10–0.62; P = 0.002). In addition, sorafenib group showed tolerable toxicity in the post-transplant setting. CONCLUSION: Sorafenib may be beneficial in patients with post-transplant HCC recurrence. The Korean Academy of Medical Sciences 2018-10-12 /pmc/articles/PMC6209769/ /pubmed/30402048 http://dx.doi.org/10.3346/jkms.2018.33.e283 Text en © 2018 The Korean Academy of Medical Sciences. https://creativecommons.org/licenses/by-nc/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (https://creativecommons.org/licenses/by-nc/4.0/) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Original Article Kang, Seong Hee Cho, Hyeki Cho, Eun Ju Lee, Jeong-Hoon Yu, Su Jong Kim, Yoon Jun Yi, Nam-Joon Lee, Kwang-Woong Suh, Kyung-Suk Yoon, Jung-Hwan Efficacy of Sorafenib for the Treatment of Post-Transplant Hepatocellular Carcinoma Recurrence |
title | Efficacy of Sorafenib for the Treatment of Post-Transplant Hepatocellular Carcinoma Recurrence |
title_full | Efficacy of Sorafenib for the Treatment of Post-Transplant Hepatocellular Carcinoma Recurrence |
title_fullStr | Efficacy of Sorafenib for the Treatment of Post-Transplant Hepatocellular Carcinoma Recurrence |
title_full_unstemmed | Efficacy of Sorafenib for the Treatment of Post-Transplant Hepatocellular Carcinoma Recurrence |
title_short | Efficacy of Sorafenib for the Treatment of Post-Transplant Hepatocellular Carcinoma Recurrence |
title_sort | efficacy of sorafenib for the treatment of post-transplant hepatocellular carcinoma recurrence |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6209769/ https://www.ncbi.nlm.nih.gov/pubmed/30402048 http://dx.doi.org/10.3346/jkms.2018.33.e283 |
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