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嵌合抗原受体 T 细胞(CAR-T)治疗复发/难治性弥漫大 B 细胞淋巴瘤:失败的原因是什么?

CD19 CAR-T cell therapy for relapsed or refractory diffuse large B cell lymphoma: Why does it fail?

机构信息

Cell Enhancement and Technologies for Immunotherapy, Children's National Hospital, Washington, DC; Department of Pediatrics, George Washington University, Washington, DC.

出版信息

Semin Hematol. 2023 Nov;60(5):329-337. doi: 10.1053/j.seminhematol.2023.11.007. Epub 2023 Dec 5.


DOI:10.1053/j.seminhematol.2023.11.007
PMID:38336529
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC10964476/
Abstract

Chimeric antigen receptor T (CAR-T) cell therapy is an effective treatment for relapsed or refractory diffuse large B cell lymphoma (DLBCL) with 3 CD19 targeting products now FDA-approved for this indication. However, up to 60% of patients ultimately progress or relapse following CAR-T cell therapy. Mechanisms of resistance to CAR-T cell therapy in patients with DLBCL are likely multifactorial and have yet to be fully elucidated. Determining patient, tumor and therapy-related factors that may predict an individual's response to CAR-T cell therapy requires ongoing analysis of data from clinical trials and real-world experience in this population. In this review we will discuss the factors identified to-date that may contribute to failure of CAR-T cell therapy in achieving durable remissions in patients with DLBCL.

摘要

嵌合抗原受体 T (CAR-T) 细胞疗法是一种有效的治疗方法,可用于治疗复发或难治性弥漫性大 B 细胞淋巴瘤 (DLBCL),目前已有 3 种针对 CD19 的产品获得 FDA 批准用于该适应证。然而,多达 60%的患者在接受 CAR-T 细胞治疗后最终会出现进展或复发。DLBCL 患者对 CAR-T 细胞治疗产生耐药的机制可能是多因素的,目前尚未完全阐明。确定可能预测个体对 CAR-T 细胞治疗反应的患者、肿瘤和治疗相关因素,需要对该人群的临床试验数据和真实世界经验进行持续分析。在这篇综述中,我们将讨论迄今为止确定的可能导致 CAR-T 细胞治疗在实现 DLBCL 患者持久缓解方面失败的因素。

相似文献

[1]
CD19 CAR-T cell therapy for relapsed or refractory diffuse large B cell lymphoma: Why does it fail?

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[2]
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[3]
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[5]
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[6]
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[7]
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[8]
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[9]
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[10]
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引用本文的文献

[1]
Effects of Mesenchymal Stem Cells on Functions of Chimeric Antigen Receptor-Expressing T Lymphocytes and Natural Killer Cells.

Cells. 2025-6-25

[2]
Targeting refractory diffuse large B cell lymphoma by CAR-WEE1 T-cells: In vitro evaluation.

Ann Hematol. 2025-3

[3]
Tumor Biology Hides Novel Therapeutic Approaches to Diffuse Large B-Cell Lymphoma: A Narrative Review.

Int J Mol Sci. 2024-10-23

本文引用的文献

[1]
Complexities in comparing the impact of costimulatory domains on approved CD19 CAR functionality.

J Transl Med. 2023-7-30

[2]
FDA Approval Summary: Axicabtagene Ciloleucel for Second-Line Treatment of Large B-Cell Lymphoma.

Clin Cancer Res. 2023-11-1

[3]
CAR T-cell therapy in large B cell lymphoma.

Hematol Oncol. 2023-6

[4]
Survival with Axicabtagene Ciloleucel in Large B-Cell Lymphoma.

N Engl J Med. 2023-7-13

[5]
CAR T-cell detection scoping review: an essential biomarker in critical need of standardization.

J Immunother Cancer. 2023-5

[6]
Monitoring of kinetics and exhaustion markers of circulating CAR-T cells as early predictive factors in patients with B-cell malignancies.

Front Immunol. 2023

[7]
CAR T-Cell Persistence Correlates with Improved Outcome in Patients with B-Cell Lymphoma.

Int J Mol Sci. 2023-3-16

[8]
Lisocabtagene maraleucel as second-line therapy for large B-cell lymphoma: primary analysis of the phase 3 TRANSFORM study.

Blood. 2023-4-6

[9]
Outcomes of first therapy after CD19-CAR-T treatment failure in large B-cell lymphoma.

Leukemia. 2023-1

[10]
Lymphoma tumor burden before chimeric antigen receptor T-Cell treatment: RECIL vs. Lugano vs. metabolic tumor assessment.

Front Oncol. 2022-9-8

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