决定异体 CAR T 细胞排斥与扩增的细胞和分子机制
Cellular and molecular mechanisms determining allogeneic CAR T cell rejection and expansion.
我们评估了11例接受单一批次cemacabtagene ansegedleucel(cema-cel)治疗的大B细胞淋巴瘤患者,cemacabtagene ansegedleucel是一种异体抗CD19 CAR T产品。
英文原题:Anti-CD19 chimeric antigen receptor T-cell therapy has less efficacy in Richter transformation than in de novo large B-cell lymphoma and transformed low-grade B-cell lymphoma.
在一项多中心回顾性研究中,我们报告了2016年4月至2023年1月期间,接受CAR T细胞治疗的RT患者(N=30)与侵袭性B细胞淋巴瘤患者(N=283)及转化性惰性非霍奇金淋巴瘤(iNHL)患者(N=141)相比的安全性和疗效。
抗CD19嵌合抗原受体(CAR)T细胞治疗慢性淋巴细胞白血病(CLL)发生Richter转化(RT)并转为侵袭性大B细胞淋巴瘤(LBCL)的疗效尚不清楚。本多中心回顾性研究报告CAR-T治疗RT患者(n=30)的安全性和疗效,并与侵袭性B细胞淋巴瘤(n=283)和惰性非霍奇金淋巴瘤转化患者(n=141)比较;研究时间为2016年4月至2023年1月。约三分之二RT患者在转化前接受CLL治疗,其中89%使用过B细胞受体或BCL2抑制剂。RT患者CAR-T毒性与其他淋巴瘤相似,未发生细胞因子释放综合征或免疫效应细胞相关神经毒性致死。RT患者100天总缓解率和完全缓解率分别为57%和47%。中位随访19个月时,RT患者中位总生存期(OS)为9.9个月,初发LBCL患者为18个月,惰性淋巴瘤转化患者尚未达到。RT患者12个月OS为45%,初发LBCL为62%,惰性淋巴瘤转化为75%。多变量分析显示,RT组织学类型、乳酸脱氢酶升高和既往治疗线数较多与OS较差相关。CAR-T可挽救部分既往接受靶向药物治疗的CLL伴RT患者,但疗效低于初发LBCL和惰性淋巴瘤转化。
The activity of anti-CD19 chimerci antigen receptor (CAR) T-cell therapy in chronic lymphocytic leukemia (CLL) with Richter's transformation (RT) to aggressive large B-cell lymphoma (LBCL) is largely unknown. In a multicenter retrospective study, we report the safety and efficacy of CAR T-cell therapy in patients with RT (N=30) compared to patients with aggressive B-cell lymphoma (N=283) and patients with transformed indolent non-Hodgkin lymphoma (iNHL) (N=141) between April 2016 and January 2023. Two-thirds of patients received prior therapy for CLL before RT and 89% of them received B-cell receptor and B-cell lymphoma 2 inhibitors. Toxicities of CAR T-cell therapy in RT were similar to other lymphomas, with no fatalities related to cytokine release syndrome or immune effector-cell associated neurotoxicity synderome. The 100-day overall response rate and complete response rates in patients with RT were 57% and 47%, respectively. With a median follow-up of 19 months, the median overall survival (OS) was 9.9 months in patients with RT compared to 18 months in de novo LBCL and not reached in patients with transformed iNHL. The OS at 12 months was 45% in patients with RT compared with 62% and 75% in patients with de novo LBCL and transformed iNHL, respectively. In a multivariate analysis, worse OS was associated with RT histology, elevated lactate dehydrogenase, and more prior lines of therapy. CAR T-cell therapy can salvage a proportion of patients with CLL and RT exposed to prior targeted agents; however, efficacy in RT is inferior compared to de novo LBCL and transformed iNHL.
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