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使用替沙格赛定治疗继发性中枢神经系统淋巴瘤的抗CD19嵌合抗原受体T细胞疗法:病例系列

Anti-CD19 Chimeric Antigen Receptor T Cell Therapy With Tisagenlecleucel for Secondary Central Nervous System Lymphoma: A Case Series.

作者信息

Dhaliwal Armaan, Mann Shivtaj

机构信息

Internal Medicine, University of Arizona College of Medicine, Tucson, USA.

Hematology and Medical Oncology, University of Arizona Cancer Center, Tucson, USA.

出版信息

Cureus. 2023 Sep 12;15(9):e45088. doi: 10.7759/cureus.45088. eCollection 2023 Sep.

Abstract

Relapsed or refractory (R/R) large B cell lymphoma (LBCL) presenting as secondary central nervous system lymphoma (SCNSL) carries a poor prognosis, with a median survival time of two to five months. Chimeric antigen receptor (CAR)-T cell therapy has been approved in R/R LBCL, but studies are ongoing to understand its efficacy and safety for SCNSL. Axicabtagene ciloleucel or tisagenlecleucel have been shown to attain high response rates in some retrospective studies; however, response durability continues to be unclear. Our study is a case series of three patients with R/R SCNSL who were treated with tisagenlecleucel. One patient achieved a complete response 30 days after CAR-T therapy but developed disease progression on day +100 imaging. The second patient had a partial response and eventual disease progression with ultimately death. The third patient died from central nervous system complications of CAR-T therapy. Two of the three patients developed immune effector cell-associated neurotoxicity syndrome grade 4 and cytokine release syndrome grade 1 toxicities. Our series of three patients demonstrates that R/R SCNSL can elicit a response with CAR-T therapy, although with a limited duration response.

摘要

复发或难治性(R/R)大B细胞淋巴瘤(LBCL)表现为继发性中枢神经系统淋巴瘤(SCNSL)时预后较差,中位生存时间为2至5个月。嵌合抗原受体(CAR)-T细胞疗法已在R/R LBCL中获得批准,但针对其治疗SCNSL的疗效和安全性的研究仍在进行中。在一些回顾性研究中,阿基仑赛或替雷利珠单抗已显示出较高的缓解率;然而,缓解的持久性仍不明确。我们的研究是一个病例系列,包含3例接受替雷利珠单抗治疗的R/R SCNSL患者。1例患者在CAR-T治疗后30天达到完全缓解,但在第100天的影像学检查中出现疾病进展。第2例患者有部分缓解,最终疾病进展并最终死亡。第3例患者死于CAR-T治疗的中枢神经系统并发症。3例患者中有2例发生了4级免疫效应细胞相关神经毒性综合征和1级细胞因子释放综合征毒性反应。我们的3例患者系列表明,R/R SCNSL接受CAR-T治疗可产生反应,尽管反应持续时间有限。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c6e3/10568653/2d3cbe182b95/cureus-0015-00000045088-i01.jpg

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