Dhaliwal Armaan, Mann Shivtaj
Internal Medicine, University of Arizona College of Medicine, Tucson, USA.
Hematology and Medical Oncology, University of Arizona Cancer Center, Tucson, USA.
Cureus. 2023 Sep 12;15(9):e45088. doi: 10.7759/cureus.45088. eCollection 2023 Sep.
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.
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。