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Immunotherapy after liver transplantation: Where are we now?

BACKGROUND: There is limited evidence on the safety of immunotherapy use after liver transplantation and its efficacy in treating post-liver transplant hepatocellular carcinoma (HCC) recurrence. AIM: To assess the safety of immunotherapy after liver transplant and its efficacy in treating post-liver...

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Autores principales: Au, Kin Pan, Chok, Kenneth Siu Ho
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Baishideng Publishing Group Inc 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8554723/
https://www.ncbi.nlm.nih.gov/pubmed/34754394
http://dx.doi.org/10.4240/wjgs.v13.i10.1267
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author Au, Kin Pan
Chok, Kenneth Siu Ho
author_facet Au, Kin Pan
Chok, Kenneth Siu Ho
author_sort Au, Kin Pan
collection PubMed
description BACKGROUND: There is limited evidence on the safety of immunotherapy use after liver transplantation and its efficacy in treating post-liver transplant hepatocellular carcinoma (HCC) recurrence. AIM: To assess the safety of immunotherapy after liver transplant and its efficacy in treating post-liver transplant HCC recurrence. METHODS: A literature review was performed to identify patients with prior liver transplantation and subsequent immunotherapy. We reviewed the rejection rate and risk factors of rejection. In patients treated for HCC, the oncological outcomes were evaluated including objective response rate, progression-free survival (PFS), and overall survival (OS). RESULTS: We identified 25 patients from 16 publications and 3 patients from our institutional database (total n = 28). The rejection rate was 32% (n = 9). Early mortality occurred in 21% (n = 6) and was mostly related to acute rejection (18%, n = 5). Patients who developed acute rejection were given immunotherapy earlier after transplantation (median 2.9 years vs 5.3 years, P = 0.02) and their graft biopsies might be more frequently programmed death ligand-1-positive (100% vs 33%, P = 0.053). Their PFS (1.0 ± 0.1 mo vs 3.5 ± 1.1 mo, P = 0.02) and OS (1.0 ± 0.1 mo vs 19.2 ± 5.5 mo, P = 0.001) compared inferiorly to patients without rejection. Among the 19 patients treated for HCC, the rejection rate was 32% (n = 6) and the overall objective response rate was 11%. The median PFS and OS were 2.5 ± 1.0 mo and 7.3 ± 2.7 mo after immunotherapy. CONCLUSION: Rejection risk is the major obstacle to immunotherapy use in liver transplant recipients. Further studies on the potential risk factors of rejection are warranted.
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spelling pubmed-85547232021-11-08 Immunotherapy after liver transplantation: Where are we now? Au, Kin Pan Chok, Kenneth Siu Ho World J Gastrointest Surg Scientometrics BACKGROUND: There is limited evidence on the safety of immunotherapy use after liver transplantation and its efficacy in treating post-liver transplant hepatocellular carcinoma (HCC) recurrence. AIM: To assess the safety of immunotherapy after liver transplant and its efficacy in treating post-liver transplant HCC recurrence. METHODS: A literature review was performed to identify patients with prior liver transplantation and subsequent immunotherapy. We reviewed the rejection rate and risk factors of rejection. In patients treated for HCC, the oncological outcomes were evaluated including objective response rate, progression-free survival (PFS), and overall survival (OS). RESULTS: We identified 25 patients from 16 publications and 3 patients from our institutional database (total n = 28). The rejection rate was 32% (n = 9). Early mortality occurred in 21% (n = 6) and was mostly related to acute rejection (18%, n = 5). Patients who developed acute rejection were given immunotherapy earlier after transplantation (median 2.9 years vs 5.3 years, P = 0.02) and their graft biopsies might be more frequently programmed death ligand-1-positive (100% vs 33%, P = 0.053). Their PFS (1.0 ± 0.1 mo vs 3.5 ± 1.1 mo, P = 0.02) and OS (1.0 ± 0.1 mo vs 19.2 ± 5.5 mo, P = 0.001) compared inferiorly to patients without rejection. Among the 19 patients treated for HCC, the rejection rate was 32% (n = 6) and the overall objective response rate was 11%. The median PFS and OS were 2.5 ± 1.0 mo and 7.3 ± 2.7 mo after immunotherapy. CONCLUSION: Rejection risk is the major obstacle to immunotherapy use in liver transplant recipients. Further studies on the potential risk factors of rejection are warranted. Baishideng Publishing Group Inc 2021-10-27 2021-10-27 /pmc/articles/PMC8554723/ /pubmed/34754394 http://dx.doi.org/10.4240/wjgs.v13.i10.1267 Text en ©The Author(s) 2021. 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: http://creativecommons.org/Licenses/by-nc/4.0/
spellingShingle Scientometrics
Au, Kin Pan
Chok, Kenneth Siu Ho
Immunotherapy after liver transplantation: Where are we now?
title Immunotherapy after liver transplantation: Where are we now?
title_full Immunotherapy after liver transplantation: Where are we now?
title_fullStr Immunotherapy after liver transplantation: Where are we now?
title_full_unstemmed Immunotherapy after liver transplantation: Where are we now?
title_short Immunotherapy after liver transplantation: Where are we now?
title_sort immunotherapy after liver transplantation: where are we now?
topic Scientometrics
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8554723/
https://www.ncbi.nlm.nih.gov/pubmed/34754394
http://dx.doi.org/10.4240/wjgs.v13.i10.1267
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