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嵌合抗原受体 T 细胞疗法治疗 B 细胞血液系统恶性肿瘤后的复发机制及治疗策略。

Relapse Mechanism and Treatment Strategy After Chimeric Antigen Receptor T-Cell Therapy in Treating B-Cell Hematological Malignancies.

机构信息

The First Central Clinical College of Tianjin Medical University, Tianjin, China.

Department of Hematology, 66571Tianjin First Central Hospital, Tianjin, China.

出版信息

Technol Cancer Res Treat. 2022 Jan-Dec;21:15330338221118413. doi: 10.1177/15330338221118413.


DOI:10.1177/15330338221118413
PMID:35989682
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC9403467/
Abstract

Over the past few decades, immunotherapy has revolutionized the modern medical oncology field. Chimeric antigen receptor (CAR)-T cell therapy has a promising curative effect in the treatment of hematological malignancies. Anti-CD19 CAR-T cells are the most mature CAR-T cells recently studied and in recent years it has achieved a complete remission rate of approximately 90% in the treatment of B-cell acute lymphoblastic leukemia (B-ALL). Although CAR-T cell therapy has greatly alleviated the disease in patients with leukemia or lymphoma, some of them still relapse after treatment. Therefore, in this article, we discuss the factors that may contribute to disease relapse following CAR-T cell therapy and summarize potential strategies to overcome these obstacles, thus providing the possibility of improving standard treatment regimens.

摘要

在过去的几十年中,免疫疗法彻底改变了现代医学肿瘤学领域。嵌合抗原受体 (CAR)-T 细胞疗法在治疗血液系统恶性肿瘤方面具有有前景的疗效。抗 CD19 CAR-T 细胞是最近研究的最成熟的 CAR-T 细胞,近年来在治疗 B 细胞急性淋巴细胞白血病 (B-ALL) 方面已达到约 90%的完全缓解率。尽管 CAR-T 细胞疗法极大地缓解了白血病或淋巴瘤患者的疾病,但其中一些患者在治疗后仍会复发。因此,在本文中,我们讨论了可能导致 CAR-T 细胞治疗后疾病复发的因素,并总结了克服这些障碍的潜在策略,从而为改善标准治疗方案提供了可能性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b95c/9403467/1b9da1f20fe4/10.1177_15330338221118413-fig3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b95c/9403467/a16246a2db05/10.1177_15330338221118413-fig1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b95c/9403467/342b6bf9251b/10.1177_15330338221118413-fig2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b95c/9403467/1b9da1f20fe4/10.1177_15330338221118413-fig3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b95c/9403467/a16246a2db05/10.1177_15330338221118413-fig1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b95c/9403467/342b6bf9251b/10.1177_15330338221118413-fig2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b95c/9403467/1b9da1f20fe4/10.1177_15330338221118413-fig3.jpg

相似文献

[1]
Relapse Mechanism and Treatment Strategy After Chimeric Antigen Receptor T-Cell Therapy in Treating B-Cell Hematological Malignancies.

Technol Cancer Res Treat. 2022

[2]
Clinical development of chimeric antigen receptor-T cell therapy for hematological malignancies.

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[3]
CAR-T cell therapy in hematological malignancies: Where are we now and where are we heading for?

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[4]
Clinical determinants of relapse following CAR-T therapy for hematologic malignancies: Coupling active strategies to overcome therapeutic limitations.

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[5]
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Stem Cell Res Ther. 2022-9-24

[6]
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[7]
Strategies to optimize chimeric antigen receptor T-cell therapy in hematologic malignancies: Chinese experience.

Haematologica. 2023-8-1

[8]
Genetic Mechanism of Leukemia Relapse Following CD19 Chimeric Antigen Receptor T Cell Therapy.

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[9]
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[10]
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引用本文的文献

[1]
Unveiling the potential of CLL-1: a promising target for AML therapy.

Biomark Res. 2025-2-12

[2]
Combination of CAR‑T cell therapy and radiotherapy: Opportunities and challenges in solid tumors (Review).

Oncol Lett. 2023-5-16

[3]
Bicistronic CAR-T cells targeting CD123 and CLL1 for AML to reduce the risk of antigen escape.

Transl Oncol. 2023-8

本文引用的文献

[1]
Optimization of metabolism to improve efficacy during CAR-T cell manufacturing.

J Transl Med. 2021-12-7

[2]
Corrigendum to <Does lineage plasticity enable escape from CAR-T cell therapy? Lessons from MLL-r leukemia'>: <[Experimental Hematology 2021; 100: 1-11]>.

Exp Hematol. 2021-11

[3]
PD-1/PD-L1 Checkpoint Inhibitors in Tumor Immunotherapy.

Front Pharmacol. 2021-9-1

[4]
Hypermethylation of CD19 promoter enables antigen-negative escape to CART-19 in vivo and in vitro.

J Immunother Cancer. 2021-8

[5]
Early-phenotype CAR-T cells for the treatment of pediatric cancers.

Ann Oncol. 2021-11

[6]
CD19/CD22 Dual-Targeted CAR T-cell Therapy for Relapsed/Refractory Aggressive B-cell Lymphoma: A Safety and Efficacy Study.

Cancer Immunol Res. 2021-9

[7]
Immune checkpoint inhibitors in lymphoma: challenges and opportunities.

Ann Transl Med. 2021-6

[8]
Anti-CD22 CAR-T Cell Therapy as a Salvage Treatment in B Cell Malignancies Refractory or Relapsed After Anti-CD19 CAR-T therapy.

Onco Targets Ther. 2021-7-2

[9]
Ciltacabtagene autoleucel, a B-cell maturation antigen-directed chimeric antigen receptor T-cell therapy in patients with relapsed or refractory multiple myeloma (CARTITUDE-1): a phase 1b/2 open-label study.

Lancet. 2021-7-24

[10]
Taking a BiTE out of the CAR T space race.

Br J Haematol. 2021-12

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