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Immunologic Features of Patients With Advanced Hepatocellular Carcinoma Before and During Sorafenib or Anti-programmed Death-1/Programmed Death-L1 Treatment
Hepatocellular carcinoma (HCC) is one of the leading causes of cancer-related death worldwide. Today, a promising treatment strategy is focused on the enhancement of antitumor immune responses by immune checkpoint modification. However, as only 20% of patients with HCC are responders, identification...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Wolters Kluwer
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6708670/ https://www.ncbi.nlm.nih.gov/pubmed/31295151 http://dx.doi.org/10.14309/ctg.0000000000000058 |
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author | Macek Jilkova, Zuzana Aspord, Caroline Kurma, Keerthi Granon, Anouck Sengel, Christian Sturm, Nathalie Marche, Patrice N. Decaens, Thomas |
author_facet | Macek Jilkova, Zuzana Aspord, Caroline Kurma, Keerthi Granon, Anouck Sengel, Christian Sturm, Nathalie Marche, Patrice N. Decaens, Thomas |
author_sort | Macek Jilkova, Zuzana |
collection | PubMed |
description | Hepatocellular carcinoma (HCC) is one of the leading causes of cancer-related death worldwide. Today, a promising treatment strategy is focused on the enhancement of antitumor immune responses by immune checkpoint modification. However, as only 20% of patients with HCC are responders, identification of predictive factors is urgently required. Therefore, for the first time, the features of the intrahepatic and circulating immune system in patients with advanced-stage HCC, before and during the treatment, were analyzed. METHODS: We collected fresh HCC biopsies, along with adjacent tumor-free liver tissues and peripheral blood samples, from 21 patients with advanced HCC. Furthermore, we performed an extensive immunomonitoring of patients with HCC treated with sorafenib or programmed death (PD)-1/PD-L1 pathway blockade using multiparametric flow cytometry. RESULTS: We observed that regardless of the treatment, low baseline intratumoral CD4(+)/CD8(+) T-cell ratio was associated with better overall survival (P = 0.0002). The baseline frequency of intratumoral PD-1(high) CD8(+) T cells was significantly lower in patients responding to sorafenib treatment than in the nonresponders (P = 0.0117), and the frequency of circulating PD-1(high) T cells increased with tumor progression (P = 0.0329). By contrast, responders to PD-1/PD-L1 pathway blockade showed a trend of high baseline frequency of intratumoral PD-1(high) CD8(+) T cells. Moreover, we observed a trend of LAG3 and TIM3 upregulation on circulating T cells in nonresponding patients to PD-1/PD-L1 pathway blockade. DISCUSSION: Immunosuppressive state, characterized by an enhanced intratumoral CD4(+)/CD8(+) T-cell ratio, was associated with poor prognosis. Additionally, our results suggest that the frequency of intratumoral PD-1(high) CD8(+) T cells may serve as a biomarker to identify which individuals will benefit from which treatment and support the use of combination strategies. |
format | Online Article Text |
id | pubmed-6708670 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Wolters Kluwer |
record_format | MEDLINE/PubMed |
spelling | pubmed-67086702019-10-10 Immunologic Features of Patients With Advanced Hepatocellular Carcinoma Before and During Sorafenib or Anti-programmed Death-1/Programmed Death-L1 Treatment Macek Jilkova, Zuzana Aspord, Caroline Kurma, Keerthi Granon, Anouck Sengel, Christian Sturm, Nathalie Marche, Patrice N. Decaens, Thomas Clin Transl Gastroenterol Article Hepatocellular carcinoma (HCC) is one of the leading causes of cancer-related death worldwide. Today, a promising treatment strategy is focused on the enhancement of antitumor immune responses by immune checkpoint modification. However, as only 20% of patients with HCC are responders, identification of predictive factors is urgently required. Therefore, for the first time, the features of the intrahepatic and circulating immune system in patients with advanced-stage HCC, before and during the treatment, were analyzed. METHODS: We collected fresh HCC biopsies, along with adjacent tumor-free liver tissues and peripheral blood samples, from 21 patients with advanced HCC. Furthermore, we performed an extensive immunomonitoring of patients with HCC treated with sorafenib or programmed death (PD)-1/PD-L1 pathway blockade using multiparametric flow cytometry. RESULTS: We observed that regardless of the treatment, low baseline intratumoral CD4(+)/CD8(+) T-cell ratio was associated with better overall survival (P = 0.0002). The baseline frequency of intratumoral PD-1(high) CD8(+) T cells was significantly lower in patients responding to sorafenib treatment than in the nonresponders (P = 0.0117), and the frequency of circulating PD-1(high) T cells increased with tumor progression (P = 0.0329). By contrast, responders to PD-1/PD-L1 pathway blockade showed a trend of high baseline frequency of intratumoral PD-1(high) CD8(+) T cells. Moreover, we observed a trend of LAG3 and TIM3 upregulation on circulating T cells in nonresponding patients to PD-1/PD-L1 pathway blockade. DISCUSSION: Immunosuppressive state, characterized by an enhanced intratumoral CD4(+)/CD8(+) T-cell ratio, was associated with poor prognosis. Additionally, our results suggest that the frequency of intratumoral PD-1(high) CD8(+) T cells may serve as a biomarker to identify which individuals will benefit from which treatment and support the use of combination strategies. Wolters Kluwer 2019-07-01 /pmc/articles/PMC6708670/ /pubmed/31295151 http://dx.doi.org/10.14309/ctg.0000000000000058 Text en © 2019 The Author(s). Published by Wolters Kluwer Health, Inc. on behalf of The American College of Gastroenterology This is an open-access article distributed under the terms of the Creative Commons Attribution-Non Commercial-No Derivatives License 4.0 (CCBY-NC-ND) (http://creativecommons.org/licenses/by-nc-nd/4.0/) , 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. |
spellingShingle | Article Macek Jilkova, Zuzana Aspord, Caroline Kurma, Keerthi Granon, Anouck Sengel, Christian Sturm, Nathalie Marche, Patrice N. Decaens, Thomas Immunologic Features of Patients With Advanced Hepatocellular Carcinoma Before and During Sorafenib or Anti-programmed Death-1/Programmed Death-L1 Treatment |
title | Immunologic Features of Patients With Advanced Hepatocellular Carcinoma Before and During Sorafenib or Anti-programmed Death-1/Programmed Death-L1 Treatment |
title_full | Immunologic Features of Patients With Advanced Hepatocellular Carcinoma Before and During Sorafenib or Anti-programmed Death-1/Programmed Death-L1 Treatment |
title_fullStr | Immunologic Features of Patients With Advanced Hepatocellular Carcinoma Before and During Sorafenib or Anti-programmed Death-1/Programmed Death-L1 Treatment |
title_full_unstemmed | Immunologic Features of Patients With Advanced Hepatocellular Carcinoma Before and During Sorafenib or Anti-programmed Death-1/Programmed Death-L1 Treatment |
title_short | Immunologic Features of Patients With Advanced Hepatocellular Carcinoma Before and During Sorafenib or Anti-programmed Death-1/Programmed Death-L1 Treatment |
title_sort | immunologic features of patients with advanced hepatocellular carcinoma before and during sorafenib or anti-programmed death-1/programmed death-l1 treatment |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6708670/ https://www.ncbi.nlm.nih.gov/pubmed/31295151 http://dx.doi.org/10.14309/ctg.0000000000000058 |
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