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嵌合抗原受体 T 细胞疗法治疗急性淋巴细胞白血病的生物标志物:个性化管理和预后预测的前景。

Biomarkers for Chimeric Antigen Receptor T Cell Therapy in Acute Lymphoblastic Leukemia: Prospects for Personalized Management and Prognostic Prediction.

机构信息

Bone Marrow Transplantation Center, The First Affiliated Hospital, Zhejiang University School of Medicine, Hangzhou, China.

Institute of Hematology, Zhejiang University, Hangzhou, China.

出版信息

Front Immunol. 2021 Feb 25;12:627764. doi: 10.3389/fimmu.2021.627764. eCollection 2021.


DOI:10.3389/fimmu.2021.627764
PMID:33717147
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7947199/
Abstract

Chimeric antigen receptor (CAR) T cell therapy represents a breakthrough in immunotherapy with the potential of ushering in a new era in cancer treatment. Remarkable therapeutic response and complete remission of this innovative management have been observed in patients with relapse/refractory acute lymphoblastic leukemia. With CAR-T cell therapy becoming widely used both in multicenter clinical trials and as a commercial treatment, therapeutic efficacy monitoring and management of toxicities will be indispensable for ensuring safety and improving overall survival. Biomarkers can act not only as effective indicators reflecting patients' baseline characteristics, CAR-T cell potency, and the immune microenvironment, but can also assess side effects during treatment. In this review, we will elaborate on a series of biomarkers associated with therapeutic response as well as treatment-related toxicities, and present their current condition and latent value with respect to the clinical utility. The combination of biomarker research and CAR-T cell therapy will contribute to establishing a safer and more powerful monitoring system and prolonging the event-free survival of patients.

摘要

嵌合抗原受体 (CAR) T 细胞疗法代表了免疫疗法的突破,有可能开创癌症治疗的新时代。在复发/难治性急性淋巴细胞白血病患者中,这种创新治疗方法观察到了显著的治疗反应和完全缓解。随着 CAR-T 细胞疗法在多中心临床试验和商业治疗中的广泛应用,治疗效果监测和毒性管理对于确保安全性和提高总生存率至关重要。生物标志物不仅可以作为反映患者基线特征、CAR-T 细胞效力和免疫微环境的有效指标,还可以评估治疗期间的副作用。在这篇综述中,我们将详细阐述一系列与治疗反应和治疗相关毒性相关的生物标志物,并介绍它们在临床应用中的现状和潜在价值。生物标志物研究与 CAR-T 细胞疗法的结合将有助于建立更安全、更强大的监测系统,并延长患者的无事件生存时间。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/709a/7947199/0bbb2ed52f88/fimmu-12-627764-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/709a/7947199/0bbb2ed52f88/fimmu-12-627764-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/709a/7947199/0bbb2ed52f88/fimmu-12-627764-g001.jpg

相似文献

[1]
Biomarkers for Chimeric Antigen Receptor T Cell Therapy in Acute Lymphoblastic Leukemia: Prospects for Personalized Management and Prognostic Prediction.

Front Immunol. 2021

[2]
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Front Immunol. 2018-2-19

[3]
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[4]
Systematic Review and Meta-analysis of CD19-Specific CAR-T Cell Therapy in Relapsed/Refractory Acute Lymphoblastic Leukemia in the Pediatric and Young Adult Population: Safety and Efficacy Outcomes.

Clin Lymphoma Myeloma Leuk. 2021-4

[5]
A novel generation 1928zT2 CAR T cells induce remission in extramedullary relapse of acute lymphoblastic leukemia.

J Hematol Oncol. 2018-2-20

[6]
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Best Pract Res Clin Haematol. 2017-9

[7]
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[8]
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[9]
Efficacy and safety of CD19 CAR T constructed with a new anti-CD19 chimeric antigen receptor in relapsed or refractory acute lymphoblastic leukemia.

J Hematol Oncol. 2020-9-7

[10]
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引用本文的文献

[1]
Adoptive cell therapy for cancer: combination strategies and biomarkers.

Front Immunol. 2025-8-1

[2]
Mathematical models and computational approaches in CAR-T therapeutics.

Front Immunol. 2025-8-1

[3]
European survey on CAR T-Cell analytical methods from apheresis to post-infusion immunomonitoring.

Front Immunol. 2025-4-24

[4]
Society for Immunotherapy of Cancer (SITC) consensus statement on essential biomarkers for immunotherapy clinical protocols.

J Immunother Cancer. 2025-3-7

[5]
A Proteomics Outlook on the Molecular Effectors of CAR-T Cell Therapy in Cancer Management.

J Proteome Res. 2025-6-6

[6]
Challenges and future perspectives for high-throughput chimeric antigen receptor T cell discovery.

Curr Opin Biotechnol. 2024-12

[7]
Identification of early predictive biomarkers for severe cytokine release syndrome in pediatric patients with chimeric antigen receptor T-cell therapy.

Front Immunol. 2024

[8]
Systemic toxicity of CAR-T therapy and potential monitoring indicators for toxicity prevention.

Front Immunol. 2024

[9]
A bibliometric and knowledge-map study on the treatment of hematological malignancies with CAR-T cells from 2012 to 2023.

Hum Vaccin Immunother. 2024-12-31

[10]
Biomarkers for prediction of CAR T therapy outcomes: current and future perspectives.

Front Immunol. 2024

本文引用的文献

[1]
Taming the beast: CRS and ICANS after CAR T-cell therapy for ALL.

Bone Marrow Transplant. 2021-3

[2]
Diagnostic biomarkers to differentiate sepsis from cytokine release syndrome in critically ill children.

Blood Adv. 2020-10-27

[3]
Characteristics of anti-CD19 CAR T cell infusion products associated with efficacy and toxicity in patients with large B cell lymphomas.

Nat Med. 2020-12

[4]
Hematopoietic recovery in patients receiving chimeric antigen receptor T-cell therapy for hematologic malignancies.

Blood Adv. 2020-8-11

[5]
Next-Generation Manufacturing Protocols Enriching T CAR T Cells Can Overcome Disease-Specific T Cell Defects in Cancer Patients.

Front Immunol. 2020

[6]
Biomarkers in individualized management of chimeric antigen receptor T cell therapy.

Biomark Res. 2020-5-11

[7]
Diagnosis and Management of Secondary HLH/MAS Following HSCT and CAR-T Cell Therapy in Adults; A Review of the Literature and a Survey of Practice Within EBMT Centres on Behalf of the Autoimmune Diseases Working Party (ADWP) and Transplant Complications Working Party (TCWP).

Front Immunol. 2020-3-31

[8]
Bispecific CAR-T cells targeting both CD19 and CD22 for therapy of adults with relapsed or refractory B cell acute lymphoblastic leukemia.

J Hematol Oncol. 2020-4-3

[9]
Dissecting the Tumor-Immune Landscape in Chimeric Antigen Receptor T-cell Therapy: Key Challenges and Opportunities for a Systems Immunology Approach.

Clin Cancer Res. 2020-7-15

[10]
Coagulation Disorders after Chimeric Antigen Receptor T Cell Therapy: Analysis of 100 Patients with Relapsed and Refractory Hematologic Malignancies.

Biol Blood Marrow Transplant. 2020-5

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