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The immunomodulatory activity of lenvatinib prompts the survival of patients with advanced hepatocellular carcinoma

BACKGROUND: Lenvatinib is a novel multiple receptor tyrosine kinase inhibitor used for hepatocellular carcinoma (HCC) treatment. Although its main function is to suppress VEGFR and FGFR pathway, its immunomodulatory activity in HCC is not elucidated. Thus, this study aimed to investigate the immunom...

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Autores principales: Zhu, Jie, Fang, Peiqi, Wang, Chong, Gu, Meixiu, Pan, Baishen, Guo, Wei, Yang, Xinrong, Wang, Beili
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8607247/
https://www.ncbi.nlm.nih.gov/pubmed/34605616
http://dx.doi.org/10.1002/cam4.4312
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author Zhu, Jie
Fang, Peiqi
Wang, Chong
Gu, Meixiu
Pan, Baishen
Guo, Wei
Yang, Xinrong
Wang, Beili
author_facet Zhu, Jie
Fang, Peiqi
Wang, Chong
Gu, Meixiu
Pan, Baishen
Guo, Wei
Yang, Xinrong
Wang, Beili
author_sort Zhu, Jie
collection PubMed
description BACKGROUND: Lenvatinib is a novel multiple receptor tyrosine kinase inhibitor used for hepatocellular carcinoma (HCC) treatment. Although its main function is to suppress VEGFR and FGFR pathway, its immunomodulatory activity in HCC is not elucidated. Thus, this study aimed to investigate the immunomodulatory capability of lenvatinib in HCC. MATERIAL AND METHODS: Totally 47 patients with HCC were enrolled in this study, and the immune cells and serum cytokine profiles before initiation of treatment and after 1 and 3 months were measured. The immune checkpoint receptors on the immune cells were also evaluated. Kaplan–Meier survival estimate and log rank tests were used to assess the prognostic value. RESULT: The frequency of T helper (Th) cells and T regulatory (Treg) cells reduced after lenvatinib treatment, while cytotoxic T lymphocyte (CTL) cells increased significantly. The cytokine profiles showed IL‐2, IL‐5, IFN‐γ increased; other cytokines including IL‐6, IL‐10, TNF‐ α and TNF‐ β decreased with lenvatinib therapy. Furthermore, the PD‐1 and TIM‐3 expressed on CTL had greatly decreased; the expression of TIM‐3 and CTLA‐4 was reduced on Treg cells as well. Besides, the new index CTL/Treg ratio was created, and low ratio was associated with the unfavorable outcome of HCC patients. CONCLUSION: Our results confirmed that lenvatinib is capable of improving patients’ immune status, saving the effector cells from exhaustion status and inhibiting the number and function of immunosuppressive cells. The novel index CTL/Treg ratio qualifies as a predictor for the outcome of patients with lenvatinib therapy.
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spelling pubmed-86072472021-11-29 The immunomodulatory activity of lenvatinib prompts the survival of patients with advanced hepatocellular carcinoma Zhu, Jie Fang, Peiqi Wang, Chong Gu, Meixiu Pan, Baishen Guo, Wei Yang, Xinrong Wang, Beili Cancer Med Clinical Cancer Research BACKGROUND: Lenvatinib is a novel multiple receptor tyrosine kinase inhibitor used for hepatocellular carcinoma (HCC) treatment. Although its main function is to suppress VEGFR and FGFR pathway, its immunomodulatory activity in HCC is not elucidated. Thus, this study aimed to investigate the immunomodulatory capability of lenvatinib in HCC. MATERIAL AND METHODS: Totally 47 patients with HCC were enrolled in this study, and the immune cells and serum cytokine profiles before initiation of treatment and after 1 and 3 months were measured. The immune checkpoint receptors on the immune cells were also evaluated. Kaplan–Meier survival estimate and log rank tests were used to assess the prognostic value. RESULT: The frequency of T helper (Th) cells and T regulatory (Treg) cells reduced after lenvatinib treatment, while cytotoxic T lymphocyte (CTL) cells increased significantly. The cytokine profiles showed IL‐2, IL‐5, IFN‐γ increased; other cytokines including IL‐6, IL‐10, TNF‐ α and TNF‐ β decreased with lenvatinib therapy. Furthermore, the PD‐1 and TIM‐3 expressed on CTL had greatly decreased; the expression of TIM‐3 and CTLA‐4 was reduced on Treg cells as well. Besides, the new index CTL/Treg ratio was created, and low ratio was associated with the unfavorable outcome of HCC patients. CONCLUSION: Our results confirmed that lenvatinib is capable of improving patients’ immune status, saving the effector cells from exhaustion status and inhibiting the number and function of immunosuppressive cells. The novel index CTL/Treg ratio qualifies as a predictor for the outcome of patients with lenvatinib therapy. John Wiley and Sons Inc. 2021-10-04 /pmc/articles/PMC8607247/ /pubmed/34605616 http://dx.doi.org/10.1002/cam4.4312 Text en © 2021 The Authors. Cancer Medicine published by John Wiley & Sons Ltd. https://creativecommons.org/licenses/by/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Clinical Cancer Research
Zhu, Jie
Fang, Peiqi
Wang, Chong
Gu, Meixiu
Pan, Baishen
Guo, Wei
Yang, Xinrong
Wang, Beili
The immunomodulatory activity of lenvatinib prompts the survival of patients with advanced hepatocellular carcinoma
title The immunomodulatory activity of lenvatinib prompts the survival of patients with advanced hepatocellular carcinoma
title_full The immunomodulatory activity of lenvatinib prompts the survival of patients with advanced hepatocellular carcinoma
title_fullStr The immunomodulatory activity of lenvatinib prompts the survival of patients with advanced hepatocellular carcinoma
title_full_unstemmed The immunomodulatory activity of lenvatinib prompts the survival of patients with advanced hepatocellular carcinoma
title_short The immunomodulatory activity of lenvatinib prompts the survival of patients with advanced hepatocellular carcinoma
title_sort immunomodulatory activity of lenvatinib prompts the survival of patients with advanced hepatocellular carcinoma
topic Clinical Cancer Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8607247/
https://www.ncbi.nlm.nih.gov/pubmed/34605616
http://dx.doi.org/10.1002/cam4.4312
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