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Therapeutic strategies for post-transplant recurrence of hepatocellular carcinoma
Despite stringent selection criteria, hepatocellular carcinoma recurrence after liver transplantation (LT) still occurs in up to 20% of cases, mostly within the first 2–3 years. No adjuvant treatments to prevent such an occurrence have been developed so far. However, a balanced use of immunosuppress...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Baishideng Publishing Group Inc
2022
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9494935/ https://www.ncbi.nlm.nih.gov/pubmed/36160651 http://dx.doi.org/10.3748/wjg.v28.i34.4929 |
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author | Sposito, Carlo Citterio, Davide Virdis, Matteo Battiston, Carlo Droz Dit Busset, Michele Flores, Maria Mazzaferro, Vincenzo |
author_facet | Sposito, Carlo Citterio, Davide Virdis, Matteo Battiston, Carlo Droz Dit Busset, Michele Flores, Maria Mazzaferro, Vincenzo |
author_sort | Sposito, Carlo |
collection | PubMed |
description | Despite stringent selection criteria, hepatocellular carcinoma recurrence after liver transplantation (LT) still occurs in up to 20% of cases, mostly within the first 2–3 years. No adjuvant treatments to prevent such an occurrence have been developed so far. However, a balanced use of immunosuppression with minimal dose of calcineurin inhibitors and possible addition of mammalian target of rapamycin inhibitors is strongly advisable. Moreover, several pre- and post-transplant predictors of recurrence have been identified and may help determine the frequency and duration of post-transplant follow-up. When recurrence occurs, the outcomes are poor with a median survival of 12 mo according to most retrospective studies. The factor that most impacts survival after recurrence is timing (within 1–2 years from LT according to different authors). Several therapeutic options may be chosen in case of recurrence, according to timing and disease presentation. Surgical treatment seems to provide a survival benefit, especially in case of late recurrence, while the benefit of locoregional treatments has been suggested only in small retrospective studies. When systemic treatment is indicated, sorafenib has been proved safe and effective, while only few data are available for lenvatinib and regorafenib in second line. The use of immune checkpoint inhibitors is controversial in this setting, given the safety warnings for the risk of acute rejection. |
format | Online Article Text |
id | pubmed-9494935 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Baishideng Publishing Group Inc |
record_format | MEDLINE/PubMed |
spelling | pubmed-94949352022-09-23 Therapeutic strategies for post-transplant recurrence of hepatocellular carcinoma Sposito, Carlo Citterio, Davide Virdis, Matteo Battiston, Carlo Droz Dit Busset, Michele Flores, Maria Mazzaferro, Vincenzo World J Gastroenterol Review Despite stringent selection criteria, hepatocellular carcinoma recurrence after liver transplantation (LT) still occurs in up to 20% of cases, mostly within the first 2–3 years. No adjuvant treatments to prevent such an occurrence have been developed so far. However, a balanced use of immunosuppression with minimal dose of calcineurin inhibitors and possible addition of mammalian target of rapamycin inhibitors is strongly advisable. Moreover, several pre- and post-transplant predictors of recurrence have been identified and may help determine the frequency and duration of post-transplant follow-up. When recurrence occurs, the outcomes are poor with a median survival of 12 mo according to most retrospective studies. The factor that most impacts survival after recurrence is timing (within 1–2 years from LT according to different authors). Several therapeutic options may be chosen in case of recurrence, according to timing and disease presentation. Surgical treatment seems to provide a survival benefit, especially in case of late recurrence, while the benefit of locoregional treatments has been suggested only in small retrospective studies. When systemic treatment is indicated, sorafenib has been proved safe and effective, while only few data are available for lenvatinib and regorafenib in second line. The use of immune checkpoint inhibitors is controversial in this setting, given the safety warnings for the risk of acute rejection. Baishideng Publishing Group Inc 2022-09-14 2022-09-14 /pmc/articles/PMC9494935/ /pubmed/36160651 http://dx.doi.org/10.3748/wjg.v28.i34.4929 Text en ©The Author(s) 2022. Published by Baishideng Publishing Group Inc. All rights reserved. https://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: https://creativecommons.org/Licenses/by-nc/4.0/ |
spellingShingle | Review Sposito, Carlo Citterio, Davide Virdis, Matteo Battiston, Carlo Droz Dit Busset, Michele Flores, Maria Mazzaferro, Vincenzo Therapeutic strategies for post-transplant recurrence of hepatocellular carcinoma |
title | Therapeutic strategies for post-transplant recurrence of hepatocellular carcinoma |
title_full | Therapeutic strategies for post-transplant recurrence of hepatocellular carcinoma |
title_fullStr | Therapeutic strategies for post-transplant recurrence of hepatocellular carcinoma |
title_full_unstemmed | Therapeutic strategies for post-transplant recurrence of hepatocellular carcinoma |
title_short | Therapeutic strategies for post-transplant recurrence of hepatocellular carcinoma |
title_sort | therapeutic strategies for post-transplant recurrence of hepatocellular carcinoma |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9494935/ https://www.ncbi.nlm.nih.gov/pubmed/36160651 http://dx.doi.org/10.3748/wjg.v28.i34.4929 |
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