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Ray of dawn: Anti-PD-1 immunotherapy enhances the chimeric antigen receptor T-cell therapy in Lymphoma patients

BACKGROUND: Chimeric antigen receptor T (CAR-T) cell therapy, a new adoptive cell therapy, has been widely used to treat lymphoma patients. Immune checkpoint blockade may improve the cytotoxicity of CAR-T cells by reducing the failure of CAR-T cells and improving antitumor activity. It has shown pro...

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Autores principales: Zhou, Yuxin, Mu, Wenjing, Wang, Chen, Zhuo, Zipeng, Xin, Yu, Li, Hongxu, Wang, Changsong
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10591343/
https://www.ncbi.nlm.nih.gov/pubmed/37872514
http://dx.doi.org/10.1186/s12885-023-11536-4
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author Zhou, Yuxin
Mu, Wenjing
Wang, Chen
Zhuo, Zipeng
Xin, Yu
Li, Hongxu
Wang, Changsong
author_facet Zhou, Yuxin
Mu, Wenjing
Wang, Chen
Zhuo, Zipeng
Xin, Yu
Li, Hongxu
Wang, Changsong
author_sort Zhou, Yuxin
collection PubMed
description BACKGROUND: Chimeric antigen receptor T (CAR-T) cell therapy, a new adoptive cell therapy, has been widely used to treat lymphoma patients. Immune checkpoint blockade may improve the cytotoxicity of CAR-T cells by reducing the failure of CAR-T cells and improving antitumor activity. It has shown promising efficacy. METHOD: We searched PubMed, the Cochrane Library, Embase and Web of Science from January 2012 to August 2022 to find data reporting the results of CAR-T cells therapy combined with PD-1 in tumor patients. An updated search was conducted in October 2023. The partial response rate (PR), complete response rate (CR), objective response rate (ORR), mortality rate, and incidence of adverse reactions were calculated. RESULTS: We analyzed 57 lymphoma patients from 5 clinical trials. The pooled partial, complete and overall response rates were 21% (95% CI 0.06–0.39, I(2) = 0.37%), 27% (95% CI 0.03–0.60, I(2) = 60.43%) and 65% (95% CI 0.23–0.98, I(2) = 76.31%), respectively. The pooled incidence of cytokine release syndrome, neutropenia, fever, and fatigue was estimated to be 57% (95% CI 0.08–0.99, I(2) = 85.20%), 47% (95% CI 0.14–0.81, I(2) = 74.17%), 59% (95% CI 0.27–0.89, I(2) = 60.23%), and 50% (95% CI 0.13–0.87, I(2) = 73.89%), respectively. CONCLUSION: CAR-T-cell therapy combined with anti-PD-1 immunotherapy in the treatment of lymphoma patients has efficacy, and the most common adverse effect is fever. REGISTRATION: The protocol was registered in prospero, with the registration number CRD42022342647. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12885-023-11536-4.
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spelling pubmed-105913432023-10-24 Ray of dawn: Anti-PD-1 immunotherapy enhances the chimeric antigen receptor T-cell therapy in Lymphoma patients Zhou, Yuxin Mu, Wenjing Wang, Chen Zhuo, Zipeng Xin, Yu Li, Hongxu Wang, Changsong BMC Cancer Research BACKGROUND: Chimeric antigen receptor T (CAR-T) cell therapy, a new adoptive cell therapy, has been widely used to treat lymphoma patients. Immune checkpoint blockade may improve the cytotoxicity of CAR-T cells by reducing the failure of CAR-T cells and improving antitumor activity. It has shown promising efficacy. METHOD: We searched PubMed, the Cochrane Library, Embase and Web of Science from January 2012 to August 2022 to find data reporting the results of CAR-T cells therapy combined with PD-1 in tumor patients. An updated search was conducted in October 2023. The partial response rate (PR), complete response rate (CR), objective response rate (ORR), mortality rate, and incidence of adverse reactions were calculated. RESULTS: We analyzed 57 lymphoma patients from 5 clinical trials. The pooled partial, complete and overall response rates were 21% (95% CI 0.06–0.39, I(2) = 0.37%), 27% (95% CI 0.03–0.60, I(2) = 60.43%) and 65% (95% CI 0.23–0.98, I(2) = 76.31%), respectively. The pooled incidence of cytokine release syndrome, neutropenia, fever, and fatigue was estimated to be 57% (95% CI 0.08–0.99, I(2) = 85.20%), 47% (95% CI 0.14–0.81, I(2) = 74.17%), 59% (95% CI 0.27–0.89, I(2) = 60.23%), and 50% (95% CI 0.13–0.87, I(2) = 73.89%), respectively. CONCLUSION: CAR-T-cell therapy combined with anti-PD-1 immunotherapy in the treatment of lymphoma patients has efficacy, and the most common adverse effect is fever. REGISTRATION: The protocol was registered in prospero, with the registration number CRD42022342647. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12885-023-11536-4. BioMed Central 2023-10-23 /pmc/articles/PMC10591343/ /pubmed/37872514 http://dx.doi.org/10.1186/s12885-023-11536-4 Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/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 licence, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons licence 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 licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data.
spellingShingle Research
Zhou, Yuxin
Mu, Wenjing
Wang, Chen
Zhuo, Zipeng
Xin, Yu
Li, Hongxu
Wang, Changsong
Ray of dawn: Anti-PD-1 immunotherapy enhances the chimeric antigen receptor T-cell therapy in Lymphoma patients
title Ray of dawn: Anti-PD-1 immunotherapy enhances the chimeric antigen receptor T-cell therapy in Lymphoma patients
title_full Ray of dawn: Anti-PD-1 immunotherapy enhances the chimeric antigen receptor T-cell therapy in Lymphoma patients
title_fullStr Ray of dawn: Anti-PD-1 immunotherapy enhances the chimeric antigen receptor T-cell therapy in Lymphoma patients
title_full_unstemmed Ray of dawn: Anti-PD-1 immunotherapy enhances the chimeric antigen receptor T-cell therapy in Lymphoma patients
title_short Ray of dawn: Anti-PD-1 immunotherapy enhances the chimeric antigen receptor T-cell therapy in Lymphoma patients
title_sort ray of dawn: anti-pd-1 immunotherapy enhances the chimeric antigen receptor t-cell therapy in lymphoma patients
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10591343/
https://www.ncbi.nlm.nih.gov/pubmed/37872514
http://dx.doi.org/10.1186/s12885-023-11536-4
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