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:Durable efficacy and manageable long-term safety of lisocabtagene maraleucel in 3L+ FL: 3-year update from TRANSCEND FL.
Durable efficacy and manageable long-term safety of lisocabtagene maraleucel in 3L+ FL: 3-year update from TRANSCEND FL.
在此,我们报告了三线或更后线(3L+)FL患者的3年随访结果(中位[范围]在研随访时间为41.5个月[0.3-54.0])。
在TRANSCEND FL主要分析中,lisocabtagene maraleucel(liso-cel)在复发/难治性(R/R)滤泡性淋巴瘤(FL)患者中显示出高缓解率和良好的安全性。需要更长时间的随访来评估缓解持久性和长期或迟发性毒性。在此,我们报告三线或更后线(3L+)FL患者的3年随访结果(中位[范围]在研随访时间,41.5个月[0.3‒54.0])。患者为接受过≥2线联合系统性治疗(包括抗CD20抗体和烷化剂)后的R/R FL。共107例患者接受了liso-cel,103例可进行疗效评估,独立审查委员会评估的总缓解率和完全缓解率(95% CI)分别为97%(92‒99)和94%(88‒98)。所有至事件发生时间结局的中位值均未达到;缓解持续时间、无进展生存期、无下次治疗时间以及总生存期的估计36个月(95% CI)率分别为70%(60‒78)、68%(58‒76)、75%(70‒80)和86%(78‒92)。在高危亚组中,包括在开始一线免疫化疗后24个月内出现疾病进展、大包块疾病或双重难治状态的患者,缓解率和36个月至事件发生时间率保持一致。纵向安全性分析显示,≥3级血细胞减少和低丙种球蛋白血症(免疫球蛋白G <500 mg/dL)逐渐减少,支持治疗(输血、生长因子、静脉注射免疫球蛋白)的使用大多限于输注后3个月内,且在短期和长期内≥3级感染的发生率持续较低。在3年随访时,单次liso-cel输注在3L+ FL患者中产生了持久的疗效和高生存率,包括在高危亚组中,同时具有有利的长期安全性特征。Clinicaltrials.gov:NCT04245839。
In the TRANSCEND FL primary analysis, lisocabtagene maraleucel (liso-cel) showed high response rates and favorable safety in patients with relapsed/refractory (R/R) follicular lymphoma (FL). Longer follow-up is needed to assess remission durability and long-term or late-onset toxicities. Here, we report 3-year follow-up results (median [range] on-study follow-up, 41.5 months [0.3‒54.0]) in patients with third-line or later (3L+) FL. Patients had R/R FL after ≥2 prior lines of combination systemic therapy, including an anti-CD20 antibody and an alkylator. A total of 107 patients received liso-cel and 103 were efficacy evaluable, with overall and complete response rates (95% CI) per independent review committee of 97% (92‒99) and 94% (88‒98), respectively. Medians were not reached for all time-to-event outcomes; estimated 36-month (95% CI) rates for duration of response, progression-free survival, time free from next treatment, and overall survival were 70% (60‒78), 68% (58‒76), 75% (70‒80), and 86% (78‒92), respectively. Response rates and 36-month time-to-event rates were consistent in high-risk subgroups, including patients with disease progression within 24 months of starting first-line immunochemotherapy, bulky disease, or double-refractory status. Longitudinal safety analyses showed decreasing grade ≥3 cytopenias and hypogammaglobulinemia (immunoglobulin G <500 mg/dL), with use of supportive care (transfusions, growth factors, intravenous immunoglobulin) mostly limited to the 3 months after infusion, and consistently low incidences of grade ≥3 infections in short- and long-term periods. At 3-year follow-up, a single liso-cel infusion delivered durable efficacy and high survival, including in high-risk subgroups, alongside a favorable long-term safety profile in patients with 3L+ FL. Clinicaltrials.gov: NCT04245839.
MEMBER ACCOUNT
登录成功会直接打开下一页。