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用于治疗高危神经母细胞瘤的抗GD2免疫疗法的进展

Advances in Anti-GD2 Immunotherapy for Treatment of High-risk Neuroblastoma.

作者信息

Voeller Julie, Sondel Paul M

机构信息

Department of Pediatrics, Division of Hematology, Oncology and Bone Marrow Transplant.

Departments of Human Oncology and Genetics and Carbone Cancer Center, University of Wisconsin, Madison, WI.

出版信息

J Pediatr Hematol Oncol. 2019 Apr;41(3):163-169. doi: 10.1097/MPH.0000000000001369.


DOI:10.1097/MPH.0000000000001369
PMID:30897608
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6430125/
Abstract

Neuroblastoma (NBL) is the most common extracranial solid tumor in pediatrics, yet overall survival is poor for high-risk cases. Immunotherapy regimens using a tumor-selective antidisialoganglioside (anti-GD2) monoclonal antibody (mAb) have been studied for several decades now, but have only recently been incorporated into standard of care treatment for patients with high-risk NBL with clear benefit. Here we review a brief history of anti-GD2-based immunotherapy, current areas of neuroblastoma research targeting GD2, and potential diagnostic and therapeutic uses targeting GD2.

摘要

神经母细胞瘤(NBL)是儿科最常见的颅外实体瘤,但高危病例的总体生存率较低。使用肿瘤选择性抗二唾液酸神经节苷脂(抗GD2)单克隆抗体(mAb)的免疫治疗方案已经研究了几十年,但直到最近才被纳入高危NBL患者的标准治疗中,并取得了明显的益处。在此,我们回顾基于抗GD2免疫治疗的简史、目前针对GD2的神经母细胞瘤研究领域,以及针对GD2的潜在诊断和治疗用途。

相似文献

[1]
Advances in Anti-GD2 Immunotherapy for Treatment of High-risk Neuroblastoma.

J Pediatr Hematol Oncol. 2019-4

[2]
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[3]
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Cancer Lett. 2009-8-28

[4]
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[5]
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Semin Oncol. 2014-10

[6]
Targeted immunotherapy for high-risk neuroblastoma--the role of monoclonal antibodies.

Ann Pharmacother. 2013-2-5

[7]
Treatment of high-risk neuroblastoma with anti-GD2 antibodies.

Clin Transl Oncol. 2010-12

[8]
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Immunotherapy. 2016-9

[9]
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Cancer Lett. 2021-4-10

[10]
GD2-targeted immunotherapy and potential value of circulating microRNAs in neuroblastoma.

J Cell Physiol. 2018-2

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Support Care Cancer. 2025-2-5

[3]
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[4]
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Transl Oncol. 2025-1

[5]
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[6]
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[7]
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Int J Mol Sci. 2024-6-7

[8]
Hu14.18K.322A Causes Direct Cell Cytotoxicity and Synergizes with Induction Chemotherapy in High-Risk Neuroblastoma.

Cancers (Basel). 2024-5-30

[9]
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Front Immunol. 2024-4-9

[10]
Toxicity Spectrum of Anti-GD2 Immunotherapy: A Real-World Study Leveraging the US Food and Drug Administration Adverse Event Reporting System.

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本文引用的文献

[1]
A Comprehensive Safety Trial of Chimeric Antibody 14.18 With GM-CSF, IL-2, and Isotretinoin in High-Risk Neuroblastoma Patients Following Myeloablative Therapy: Children's Oncology Group Study ANBL0931.

Front Immunol. 2018-6-18

[2]
Tumor-Specific Inhibition of Vaccination by Distant Untreated Tumor Sites.

Cancer Immunol Res. 2018-5-10

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Tolerability, response and outcome of high-risk neuroblastoma patients treated with long-term infusion of anti-GD antibody ch14.18/CHO.

MAbs. 2017-12-5

[4]
Neuroblastoma Patients' KIR and KIR-Ligand Genotypes Influence Clinical Outcome for Dinutuximab-based Immunotherapy: A Report from the Children's Oncology Group.

Clin Cancer Res. 2017-10-2

[5]
A Pilot Trial of Humanized Anti-GD2 Monoclonal Antibody (hu14.18K322A) with Chemotherapy and Natural Killer Cells in Children with Recurrent/Refractory Neuroblastoma.

Clin Cancer Res. 2017-9-22

[6]
Tumor Antigen and Receptor Densities Regulate Efficacy of a Chimeric Antigen Receptor Targeting Anaplastic Lymphoma Kinase.

Mol Ther. 2017-7-1

[7]
Irinotecan-temozolomide with temsirolimus or dinutuximab in children with refractory or relapsed neuroblastoma (COG ANBL1221): an open-label, randomised, phase 2 trial.

Lancet Oncol. 2017-7

[8]
TGFβR1 Blockade with Galunisertib (LY2157299) Enhances Anti-Neuroblastoma Activity of the Anti-GD2 Antibody Dinutuximab (ch14.18) with Natural Killer Cells.

Clin Cancer Res. 2017-2-1

[9]
Efficient Killing of High Risk Neuroblastoma Using Natural Killer Cells Activated by Plasmacytoid Dendritic Cells.

PLoS One. 2016-10-7

[10]
Lack of immunocytological GD2 expression on neuroblastoma cells in bone marrow at diagnosis, during treatment, and at recurrence.

Pediatr Blood Cancer. 2017-1

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