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Irreversible electroporation plus allogenic Vγ9Vδ2 T cells enhances antitumor effect for locally advanced pancreatic cancer patients

Immunotherapy has limited efficacy against locally advanced pancreatic cancer (LAPC) due to the presence of an immunosuppressive microenvironment (ISM). Irreversible electroporation (IRE) can not only induce immunogenic cell death, but also alleviate immunosuppression. This study aimed to investigat...

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Autores principales: Lin, Mao, Zhang, Xiaoyan, Liang, Shuzhen, Luo, Haihua, Alnaggar, Mohammed, Liu, Aihua, Yin, Zhinan, Chen, Jibing, Niu, Lizhi, Jiang, Yong
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7582168/
https://www.ncbi.nlm.nih.gov/pubmed/33093457
http://dx.doi.org/10.1038/s41392-020-00260-1
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author Lin, Mao
Zhang, Xiaoyan
Liang, Shuzhen
Luo, Haihua
Alnaggar, Mohammed
Liu, Aihua
Yin, Zhinan
Chen, Jibing
Niu, Lizhi
Jiang, Yong
author_facet Lin, Mao
Zhang, Xiaoyan
Liang, Shuzhen
Luo, Haihua
Alnaggar, Mohammed
Liu, Aihua
Yin, Zhinan
Chen, Jibing
Niu, Lizhi
Jiang, Yong
author_sort Lin, Mao
collection PubMed
description Immunotherapy has limited efficacy against locally advanced pancreatic cancer (LAPC) due to the presence of an immunosuppressive microenvironment (ISM). Irreversible electroporation (IRE) can not only induce immunogenic cell death, but also alleviate immunosuppression. This study aimed to investigate the antitumor efficacy of IRE plus allogeneic γδ T cells in LAPC patients. A total of 62 patients who met the eligibility criteria were enrolled in this trial, then randomized into two groups (A: n = 30 and B: n = 32). All patients received IRE therapy and after receiving IRE, the group A patients received at least two cycles of γδ T-cell infusion as one course continuously. Group A patients had better survival than group B patients (median OS: 14.5 months vs. 11 months; median PFS: 11 months vs. 8.5 months). Moreover, the group A patients treated with multiple courses of γδ T-cell infusion had longer OS (17 months) than those who received a single course (13.5 months). IRE combined with allogeneic γδ T-cell infusion is a promising strategy to enhance the antitumor efficacy in LAPC patients, yielding extended survival benefits. ClinicalTrials.gov ID: NCT03180437.
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spelling pubmed-75821682020-10-26 Irreversible electroporation plus allogenic Vγ9Vδ2 T cells enhances antitumor effect for locally advanced pancreatic cancer patients Lin, Mao Zhang, Xiaoyan Liang, Shuzhen Luo, Haihua Alnaggar, Mohammed Liu, Aihua Yin, Zhinan Chen, Jibing Niu, Lizhi Jiang, Yong Signal Transduct Target Ther Article Immunotherapy has limited efficacy against locally advanced pancreatic cancer (LAPC) due to the presence of an immunosuppressive microenvironment (ISM). Irreversible electroporation (IRE) can not only induce immunogenic cell death, but also alleviate immunosuppression. This study aimed to investigate the antitumor efficacy of IRE plus allogeneic γδ T cells in LAPC patients. A total of 62 patients who met the eligibility criteria were enrolled in this trial, then randomized into two groups (A: n = 30 and B: n = 32). All patients received IRE therapy and after receiving IRE, the group A patients received at least two cycles of γδ T-cell infusion as one course continuously. Group A patients had better survival than group B patients (median OS: 14.5 months vs. 11 months; median PFS: 11 months vs. 8.5 months). Moreover, the group A patients treated with multiple courses of γδ T-cell infusion had longer OS (17 months) than those who received a single course (13.5 months). IRE combined with allogeneic γδ T-cell infusion is a promising strategy to enhance the antitumor efficacy in LAPC patients, yielding extended survival benefits. ClinicalTrials.gov ID: NCT03180437. Nature Publishing Group UK 2020-10-23 /pmc/articles/PMC7582168/ /pubmed/33093457 http://dx.doi.org/10.1038/s41392-020-00260-1 Text en © The Author(s) 2020 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Lin, Mao
Zhang, Xiaoyan
Liang, Shuzhen
Luo, Haihua
Alnaggar, Mohammed
Liu, Aihua
Yin, Zhinan
Chen, Jibing
Niu, Lizhi
Jiang, Yong
Irreversible electroporation plus allogenic Vγ9Vδ2 T cells enhances antitumor effect for locally advanced pancreatic cancer patients
title Irreversible electroporation plus allogenic Vγ9Vδ2 T cells enhances antitumor effect for locally advanced pancreatic cancer patients
title_full Irreversible electroporation plus allogenic Vγ9Vδ2 T cells enhances antitumor effect for locally advanced pancreatic cancer patients
title_fullStr Irreversible electroporation plus allogenic Vγ9Vδ2 T cells enhances antitumor effect for locally advanced pancreatic cancer patients
title_full_unstemmed Irreversible electroporation plus allogenic Vγ9Vδ2 T cells enhances antitumor effect for locally advanced pancreatic cancer patients
title_short Irreversible electroporation plus allogenic Vγ9Vδ2 T cells enhances antitumor effect for locally advanced pancreatic cancer patients
title_sort irreversible electroporation plus allogenic vγ9vδ2 t cells enhances antitumor effect for locally advanced pancreatic cancer patients
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7582168/
https://www.ncbi.nlm.nih.gov/pubmed/33093457
http://dx.doi.org/10.1038/s41392-020-00260-1
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