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:Five-year survival outcomes of lisocabtagene maraleucel in R/R LBCL from the TRANSCEND NHL 001 study.
这些数据支持liso-cel在R/R LBCL患者中的治愈潜力。
我们展示了TRANSCEND NHL 001(TRANSCEND)中复发或难治性(R/R)大B细胞淋巴瘤(LBCL)患者的5年生存结果,包括来自单独长期随访(LTFU)研究的数据。总体而言,345例患者接受了白细胞分离术,270例接受了lisocabtagene maraleucel(liso-cel)治疗。在257例可评估疗效的患者中,中位总生存期(OS)为27.5个月(95%置信区间[CI],16.2-47.3;白细胞分离术集:15.2个月;95% CI,11.5-23.4);估计5年OS为38%(95% CI,32-45;白细胞分离术集:33%;95% CI,28-39)。中位疾病特异性生存期(DSS;排除与疾病进展无关的死亡)为67.8个月(95% CI,23.5至未达到[NR];白细胞分离术集:27.4个月;95% CI,14.4-69.7);估计5年DSS为52%(95% CI,45-59;白细胞分离术集:47%;95% CI,41-52)。在TRANSCEND中可评估疗效、研究完成时存活并纳入LTFU的患者中(n = 84),中位OS和DSS均为NR(95% CI,NR至NR);估计5年OS和DSS分别为78%(95% CI,67-86)和92%(95% CI,84-97)。大多数死亡发生在输注后≤2年;未观察到新的安全性信号,晚期严重感染和第二原发恶性肿瘤发生率较低。这些数据支持liso-cel在R/R LBCL患者中的治愈潜力。该试验注册于www.clinicaltrials.gov,编号为NCT02631044和NCT03435796。
We present 5-year survival results in patients with relapsed or refractory (R/R) large B-cell lymphoma (LBCL) from TRANSCEND NHL 001 (TRANSCEND), including data from the separate long-term follow-up (LTFU) study. Overall, 345 patients were leukapheresed and 270 received lisocabtagene maraleucel (liso-cel). Among 257 patients who were efficacy-evaluable, median overall survival (OS) was 27.5 months (95% confidence interval [CI], 16.2-47.3; leukapheresed set: 15.2 months; 95% CI, 11.5-23.4); estimated 5-year OS was 38% (95% CI, 32-45; leukapheresed set: 33%; 95% CI, 28-39). Median disease-specific survival (DSS; excludes deaths unrelated to disease progression) was 67.8 months (95% CI, 23.5 to not reached [NR]; leukapheresed set: 27.4 months; 95% CI, 14.4-69.7]); estimated 5-year DSS was 52% (95% CI, 45-59; leukapheresed set: 47%; 95% CI, 41-52). Among patients from TRANSCEND who were efficacy-evaluable, alive at study completion, and enrolled in the LTFU (n = 84), median OS and DSS were NR (95% CI, NR to NR); estimated 5-year OS and DSS were 78% (95% CI, 67-86) and 92% (95% CI, 84-97), respectively. Most deaths occurred ≤2 years after infusion; no new safety signals were observed with low rates of late severe infections and second primary malignancies. These data support the curative potential of liso-cel in patients with R/R LBCL. This trial was registered at www.clinicaltrials.gov as NCT02631044 and NCT03435796.
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