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经地西他滨预处理的双靶点嵌合抗原受体 T 细胞(CD19/CD22 CAR-T)治疗联合 PD-1 和 BTK 抑制剂维持治疗难治性原发性中枢神经系统淋巴瘤患者获得长期完全缓解。

Long-term Complete Remission of Decitabine-Primed Tandem CD19/CD22 CAR-T Therapy with PD-1 and BTK Inhibitors Maintenance in a Refractory Primary Central Nervous System Lymphoma Patient.

机构信息

College of Pharmaceutical Sciences Soochow University, The First Affiliated Hospital of Soochow University, Suzhou, China.

National Clinical Research Center for Hematologic Diseases, Jiangsu Institute of Hematology, The First Affiliated Hospital of Soochow University, Suzhou, China.

出版信息

Cancer Res Treat. 2023 Oct;55(4):1363-1368. doi: 10.4143/crt.2023.371. Epub 2023 Jun 14.


DOI:10.4143/crt.2023.371
PMID:37321275
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC10582536/
Abstract

Primary central nervous system lymphoma (PCNSL) is a rare and aggressive non-Hodgkin's lymphoma that affects the brain, eyes, cerebrospinal fluid, or spinal cord without systemic involvement. The outcome of patients with PCNSL is worse compared to patients with systemic diffuse large B-cell lymphoma. Given potential mortality associated with severe immune effector cell-associated neurotoxicity syndrome (ICANS), patients with PCNSL have been excluded from most clinical trials involving chimeric antigen receptor T-cell (CAR-T) therapy initially. Here, we report for the first time to apply decitabine-primed tandem CD19/CD22 dual-targeted CAR-T therapy with programmed cell death-1 (PD-1) and Bruton's tyrosine kinase (BTK) inhibitors maintenance in one patient with multiline-resistant refractory PCNSL and the patient has maintained complete remission (CR) for a 35-month follow-up period. This case represents the first successful treatment of multiline resistant refractory PCNSL with long-term CR and without inducing ICANS under tandem CD19/CD22 bispecific CAR-T therapy followed by maintenance therapy with PD-1 and BTK inhibitors. This study shows tremendous potential in the treatment of PCNSL and offers a look toward ongoing clinical studies.

摘要

原发性中枢神经系统淋巴瘤(PCNSL)是一种罕见且侵袭性的非霍奇金淋巴瘤,影响大脑、眼睛、脑脊液或脊髓而无全身受累。与全身弥漫性大 B 细胞淋巴瘤患者相比,PCNSL 患者的预后更差。鉴于严重免疫效应细胞相关神经毒性综合征(ICANS)相关的潜在死亡率,最初大多数涉及嵌合抗原受体 T 细胞(CAR-T)治疗的临床试验都排除了 PCNSL 患者。在这里,我们首次报告了一例多线耐药难治性 PCNSL 患者应用去甲基化药物-预处理的串联 CD19/CD22 双靶点 CAR-T 治疗,并联合程序性细胞死亡蛋白 1(PD-1)和布鲁顿酪氨酸激酶(BTK)抑制剂维持治疗。该患者在 35 个月的随访期内保持完全缓解(CR)。该病例代表了首例多线耐药难治性 PCNSL 在串联 CD19/CD22 双特异性 CAR-T 治疗后联合 PD-1 和 BTK 抑制剂维持治疗下,无 ICANS 诱导且长期 CR 的成功治疗。该研究为 PCNSL 的治疗提供了巨大的潜力,并为正在进行的临床研究提供了参考。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1a29/10582536/cc3eb27d888f/crt-2023-371f4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1a29/10582536/4c3734bfc69f/crt-2023-371f1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1a29/10582536/2038ce66dded/crt-2023-371f2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1a29/10582536/a2507eb8d94a/crt-2023-371f3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1a29/10582536/cc3eb27d888f/crt-2023-371f4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1a29/10582536/4c3734bfc69f/crt-2023-371f1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1a29/10582536/2038ce66dded/crt-2023-371f2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1a29/10582536/a2507eb8d94a/crt-2023-371f3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1a29/10582536/cc3eb27d888f/crt-2023-371f4.jpg

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引用本文的文献

[1]
From molecular design to clinical translation: dual-targeted CAR-T strategies in cancer immunotherapy.

Int J Biol Sci. 2025-3-31

[2]
New hopes and challenges in targeted therapy and immunotherapy for primary central nervous system lymphoma.

Front Immunol. 2025-2-18

[3]
The synergistic immunotherapeutic impact of engineered CAR-T cells with PD-1 blockade in lymphomas and solid tumors: a systematic review.

Front Immunol. 2024

本文引用的文献

[1]
Case report: CD19-directed CAR-T cell therapy combined with BTK inhibitor and PD-1 antibody against secondary central nervous system lymphoma.

Front Immunol. 2022

[2]
Decitabine-primed tandem CD19/CD22 CAR-T therapy in relapsed/refractory diffuse large B-cell lymphoma patients.

Front Immunol. 2022

[3]
Safety and efficacy of tisagenlecleucel in primary CNS lymphoma: a phase 1/2 clinical trial.

Blood. 2022-4-14

[4]
Primary central nervous system lymphoma.

Blood. 2022-9-1

[5]
CD19-directed CAR T-cell therapy for treatment of primary CNS lymphoma.

Blood Adv. 2021-10-26

[6]
CAR T-Cells for CNS Lymphoma: Driving into New Terrain?

Cancers (Basel). 2021-5-20

[7]
Current and emerging therapies for primary central nervous system lymphoma.

Biomark Res. 2021-5-6

[8]
CAR T-Cell Therapy Is Effective but Not Long-Lasting in B-Cell Lymphoma of the Brain.

Front Oncol. 2020-8-4

[9]
Optimized tandem CD19/CD20 CAR-engineered T cells in refractory/relapsed B-cell lymphoma.

Blood. 2020-10-1

[10]
CD19 and CD70 Dual-Target Chimeric Antigen Receptor T-Cell Therapy for the Treatment of Relapsed and Refractory Primary Central Nervous System Diffuse Large B-Cell Lymphoma.

Front Oncol. 2019-12-4

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