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tisagenlecleucel CAR T 细胞疗法治疗中枢神经系统淋巴瘤。

Tisagenlecleucel CAR T-cell therapy in secondary CNS lymphoma.

机构信息

Cellular Immunotherapy Program, Massachusetts General Hospital Cancer Center.

Blood and Marrow Transplant Program, Massachusetts General Hospital.

出版信息

Blood. 2019 Sep 12;134(11):860-866. doi: 10.1182/blood.2019001694. Epub 2019 Jul 18.

DOI:10.1182/blood.2019001694
PMID:31320380
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7022436/
Abstract

Chimeric antigen receptor (CAR) T cells targeting CD19 have emerged as a leading engineered T-cell therapy for relapsed/refractory B-cell non-Hodgkin lymphoma. The phase 1/2 clinical trials that led to US Food and Drug Administration approval excluded patients with central nervous system (CNS) involvement, due to strict eligibility criteria. Here, we report on our institutional experience with 8 secondary CNS lymphoma patients treated with commercial tisagenlecleucel. No patient experienced greater than grade 1 neurotoxicity, and no patient required tocilizumab or steroids for CAR T-cell-mediated toxicities. Biomarker analysis suggested CAR T-cell expansion, despite the absence of systemic disease, and early response assessments demonstrated activity of IV infused CAR T cells within the CNS space.

摘要

嵌合抗原受体 (CAR) T 细胞靶向 CD19 已成为治疗复发性/难治性 B 细胞非霍奇金淋巴瘤的主要工程 T 细胞疗法。导致美国食品和药物管理局批准的 1/2 期临床试验排除了中枢神经系统 (CNS) 受累的患者,这是由于严格的资格标准。在这里,我们报告了我们机构使用商业 tisagenlecleucel 治疗 8 例继发性中枢神经系统淋巴瘤患者的经验。没有患者出现大于 1 级的神经毒性,也没有患者因 CAR T 细胞介导的毒性而需要使用托珠单抗或皮质类固醇。生物标志物分析表明尽管没有系统性疾病,但存在 CAR T 细胞扩增,并且早期反应评估表明 IV 输注的 CAR T 细胞在中枢神经系统空间内具有活性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/50f6/7022436/962397a7bd2c/bloodBLD2019001694absf1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/50f6/7022436/962397a7bd2c/bloodBLD2019001694absf1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/50f6/7022436/962397a7bd2c/bloodBLD2019001694absf1.jpg

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