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嵌合抗原受体 T 细胞治疗恶性肿瘤的严重不良事件及应对策略。

Serious adverse events and coping strategies of CAR-T cells in the treatment of malignant tumors.

机构信息

Department of Orthopedics, Honghui Hospital, Xi'an Jiaotong University, Xi'an, China.

出版信息

Front Immunol. 2022 Dec 8;13:1079181. doi: 10.3389/fimmu.2022.1079181. eCollection 2022.


DOI:10.3389/fimmu.2022.1079181
PMID:36569917
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC9772271/
Abstract

Chimeric antigen receptor T (CAR-T) cells technology has been successfully used in the treatment of B cell-derived hematological tumors and multiple myeloma. CAR-T cells are also being studied in a variety of solid tumors. Current clinical reports on CAR-T cells in the treatment of malignant tumors are abundant. The tumor-killing activity of CAR-T cells and the unique adverse effects of CAR-T cells have been confirmed by many studies. There is evidence that serious adverse events can be life-threatening. CAR-T cells therapy is increasingly used in clinical settings, so it is important to pay attention to its serious adverse events. In this review, we summarized the serious adverse events of CAR-T cells in the treatment of malignant tumors by reading literature and searching relevant clinical studies, and discussed the management and treatment of serious adverse events in an effort to provide theoretical support for clinicians who deal with such patients.

摘要

嵌合抗原受体 T (CAR-T) 细胞技术已成功应用于治疗 B 细胞来源的血液系统肿瘤和多发性骨髓瘤。CAR-T 细胞也正在多种实体瘤中进行研究。目前关于 CAR-T 细胞治疗恶性肿瘤的临床报告很多。许多研究证实了 CAR-T 细胞的杀伤活性和 CAR-T 细胞的独特不良反应。有证据表明,严重的不良反应可能危及生命。CAR-T 细胞疗法越来越多地应用于临床,因此,关注其严重的不良反应非常重要。本综述通过阅读文献和检索相关临床研究,总结了 CAR-T 细胞治疗恶性肿瘤的严重不良事件,并对严重不良事件的处理和治疗进行了讨论,以期为处理此类患者的临床医生提供理论支持。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6dd8/9772271/3d117658611f/fimmu-13-1079181-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6dd8/9772271/e702d06ea379/fimmu-13-1079181-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6dd8/9772271/3d117658611f/fimmu-13-1079181-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6dd8/9772271/e702d06ea379/fimmu-13-1079181-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6dd8/9772271/3d117658611f/fimmu-13-1079181-g002.jpg

相似文献

[1]
Serious adverse events and coping strategies of CAR-T cells in the treatment of malignant tumors.

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[2]
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[2]
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[3]
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[4]
CAR T-Cell Therapy Unveiled: Navigating Beyond CRS and ICANS to Address Delayed Complications and Optimize Management Strategies.

J Adv Pract Oncol. 2025-1-29

[5]
Challenges and overcoming strategies in CAR-T cell therapy for pediatric neuroblastoma.

World J Pediatr. 2025-2

[6]
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Front Immunol. 2024

[7]
CAR-T therapy pulmonary adverse event profile: a pharmacovigilance study based on FAERS database (2017-2023).

Front Pharmacol. 2024-8-21

[8]
Application of CAR-T cell therapy targeting mesothelin in solid tumor treatment.

Discov Oncol. 2024-7-18

[9]
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[10]
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Exp Hematol Oncol. 2024-4-25

本文引用的文献

[1]
Research advance of natural products in tumor immunotherapy.

Front Immunol. 2022

[2]
Risk of infection in patients with hematological malignancies receiving CAR T-cell therapy: systematic review and meta-analysis.

Expert Rev Anti Infect Ther. 2022-11

[3]
Cardiotoxicity Associated With Chimeric Antigen Receptor (CAR)-T Cell Therapy for Hematologic Malignancies: A Systematic Review.

Cureus. 2022-8-19

[4]
Cytopenia after chimeric antigen receptor T cell immunotherapy in relapsed or refractory lymphoma.

Front Immunol. 2022

[5]
Investigation of CRS-associated cytokines in CAR-T therapy with meta-GNN and pathway crosstalk.

BMC Bioinformatics. 2022-9-13

[6]
Non-viral, specifically targeted CAR-T cells achieve high safety and efficacy in B-NHL.

Nature. 2022-9

[7]
The efficacy and safety of chimeric antigen receptor T cells in digestive system cancers: a systematic review and meta-analysis.

Ann Transl Med. 2022-5

[8]
Emerging approaches for preventing cytokine release syndrome in CAR-T cell therapy.

J Mater Chem B. 2022-9-28

[9]
Efficacy and safety of chimeric antigen receptor T-cells treatment in central nervous system lymphoma: a PRISMA-compliant single-arm meta-analysis.

Cancer Immunol Immunother. 2023-1

[10]
Cardiovascular Toxicities with Chimeric Antigen Receptor T-cell Therapy.

Curr Cardiol Rev. 2023

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