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Case Report: Successful liver transplantation after achieving complete clinical remission of advanced HCC with Atezolizumab plus Bevacizumab combination therapy
BACKGROUND: Atezolizumab plus Bevacizumab combination therapy has recently emerged as the new standard of care for unresectable HCC. Significant tumor burden reduction can be observed under that treatment, raising the question of liver transplantation (LT). The safety of another immune checkpoint in...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2023
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10291060/ https://www.ncbi.nlm.nih.gov/pubmed/37377975 http://dx.doi.org/10.3389/fimmu.2023.1205997 |
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author | Chouik, Yasmina Erard, Domitille Demian, Hassan Schulz, Thomas Mazard, Tessa Hartig-Lavie, Kerstin Antonini, Teresa Mabrut, Jean-Yves Mohkam, Kayvan Rode, Agnès Merle, Philippe |
author_facet | Chouik, Yasmina Erard, Domitille Demian, Hassan Schulz, Thomas Mazard, Tessa Hartig-Lavie, Kerstin Antonini, Teresa Mabrut, Jean-Yves Mohkam, Kayvan Rode, Agnès Merle, Philippe |
author_sort | Chouik, Yasmina |
collection | PubMed |
description | BACKGROUND: Atezolizumab plus Bevacizumab combination therapy has recently emerged as the new standard of care for unresectable HCC. Significant tumor burden reduction can be observed under that treatment, raising the question of liver transplantation (LT). The safety of another immune checkpoint inhibitor (ICI), nivolumab, is unclear in the pre-transplant setting. METHOD: We report the case of a 57-y old man, with initial unresectable multinodular HCC contraindicated to LT and locoregional therapies, who achieves complete tumor response after Atezolizumab/Bevacizumab, and subsequently underwent LT for liver failure. RESULTS: Explant analysis revealed complete pathological response with no tumor remnant. The patient suffered from several post-operative complications but no HCC recurrence or biopsy-proven acute rejection occurred 10 months after LT. CONCLUSIONS: Atezolizumab/Bevacizumab therapy may enable complete pathological response of advanced HCC. Safety of prolonged treatment need to be assessed. |
format | Online Article Text |
id | pubmed-10291060 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-102910602023-06-27 Case Report: Successful liver transplantation after achieving complete clinical remission of advanced HCC with Atezolizumab plus Bevacizumab combination therapy Chouik, Yasmina Erard, Domitille Demian, Hassan Schulz, Thomas Mazard, Tessa Hartig-Lavie, Kerstin Antonini, Teresa Mabrut, Jean-Yves Mohkam, Kayvan Rode, Agnès Merle, Philippe Front Immunol Immunology BACKGROUND: Atezolizumab plus Bevacizumab combination therapy has recently emerged as the new standard of care for unresectable HCC. Significant tumor burden reduction can be observed under that treatment, raising the question of liver transplantation (LT). The safety of another immune checkpoint inhibitor (ICI), nivolumab, is unclear in the pre-transplant setting. METHOD: We report the case of a 57-y old man, with initial unresectable multinodular HCC contraindicated to LT and locoregional therapies, who achieves complete tumor response after Atezolizumab/Bevacizumab, and subsequently underwent LT for liver failure. RESULTS: Explant analysis revealed complete pathological response with no tumor remnant. The patient suffered from several post-operative complications but no HCC recurrence or biopsy-proven acute rejection occurred 10 months after LT. CONCLUSIONS: Atezolizumab/Bevacizumab therapy may enable complete pathological response of advanced HCC. Safety of prolonged treatment need to be assessed. Frontiers Media S.A. 2023-06-12 /pmc/articles/PMC10291060/ /pubmed/37377975 http://dx.doi.org/10.3389/fimmu.2023.1205997 Text en Copyright © 2023 Chouik, Erard, Demian, Schulz, Mazard, Hartig-Lavie, Antonini, Mabrut, Mohkam, Rode and Merle https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
spellingShingle | Immunology Chouik, Yasmina Erard, Domitille Demian, Hassan Schulz, Thomas Mazard, Tessa Hartig-Lavie, Kerstin Antonini, Teresa Mabrut, Jean-Yves Mohkam, Kayvan Rode, Agnès Merle, Philippe Case Report: Successful liver transplantation after achieving complete clinical remission of advanced HCC with Atezolizumab plus Bevacizumab combination therapy |
title | Case Report: Successful liver transplantation after achieving complete clinical remission of advanced HCC with Atezolizumab plus Bevacizumab combination therapy |
title_full | Case Report: Successful liver transplantation after achieving complete clinical remission of advanced HCC with Atezolizumab plus Bevacizumab combination therapy |
title_fullStr | Case Report: Successful liver transplantation after achieving complete clinical remission of advanced HCC with Atezolizumab plus Bevacizumab combination therapy |
title_full_unstemmed | Case Report: Successful liver transplantation after achieving complete clinical remission of advanced HCC with Atezolizumab plus Bevacizumab combination therapy |
title_short | Case Report: Successful liver transplantation after achieving complete clinical remission of advanced HCC with Atezolizumab plus Bevacizumab combination therapy |
title_sort | case report: successful liver transplantation after achieving complete clinical remission of advanced hcc with atezolizumab plus bevacizumab combination therapy |
topic | Immunology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10291060/ https://www.ncbi.nlm.nih.gov/pubmed/37377975 http://dx.doi.org/10.3389/fimmu.2023.1205997 |
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