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:Health-related quality of life in patients given ciltacabtagene autoleucel for relapsed or refractory multiple myeloma (CARTITUDE-1): a phase 1b-2, open-label study.
这些持久的HRQOL改善与临床发现一致,即单次cilta-cel输注在重度预处理的复发或难治性多发性骨髓瘤患者中产生了显著且持久的缓解。这些结果支持在复发或难治性多发性骨髓瘤患者中使用cilta-cel。
CARTITUDE-1是一项1b-2期研究,评估ciltacabtagene autoleucel(cilta-cel),一种具有两个靶向B细胞成熟抗原的单域抗体的CAR-T 细胞疗法,用于复发或难治性多发性骨髓瘤患者。主要疗效结局此前已有报告。在此,我们报告使用患者报告结局评估的健康相关生活质量(HRQOL)次要结局。
这项单臂、开放标签的1b-2期研究在美国16个中心进行。患者年龄为18岁或以上,诊断为多发性骨髓瘤,东部肿瘤协作组体能状态评分为1或以下,既往接受过三线或以上治疗,或对蛋白酶体抑制剂和免疫调节药物双重难治,并且已接受过蛋白酶体抑制剂、免疫调节药物和抗CD38抗体。在淋巴细胞清除后5-7天给予单次cilta-cel输注(目标剂量0 75 10 6 CAR + T细胞/kg)。患者报告结局使用欧洲癌症研究与治疗组织(EORTC)生活质量问卷核心30项、EORTC骨髓瘤模块中预先指定的项目以及EuroQol五维描述系统问卷进行评估。患者报告结局中具有临床意义的改变通过基于锚定的最小重要差异来定义。该试验注册于ClinicalTrials.gov,NCT03548207。该试验已完成,但正在纳入一项长期随访研究。
2018年7月16日至2019年10月7日期间,78例患者入组并在研究的2期部分接受了单采。68例患者接受了治疗(43例[63%]男性,49例[72%]白人),并对其患者报告结局进行了评估(中位随访16.9个月,IQR 15.7-17.5)。输注后,观察到一过性下降,随后总体健康状况(从基线至第464天的平均变化 +8.0分,SD 20.9)、躯体功能(+4.6分,21.1)和情绪功能量表(+1.9分,23.7)随时间改善,而症状评分下降(疼痛 -14.1,SD 31.5;疲乏 -15.4;SD 29.5),表明接受cilta-cel治疗后患者HRQOL改善。
BACKGROUND: CARTITUDE-1 is a phase 1b-2 study evaluating ciltacabtagene autoleucel (cilta-cel), a chimeric antigen receptor T cell therapy with two B-cell maturation antigen-targeting single-domain antibodies, in patients with relapsed or refractory multiple myeloma. Primary efficacy outcomes have previously been reported. Here, we report health-related quality of life (HRQOL) secondary outcomes evaluated using patient-reported outcomes. METHODS: This single-arm, open-label, phwase 1b-2 study was done at 16 centres in the USA. Patients were aged 18 years or older with diagnosis of multiple myeloma and Eastern Cooperative Oncology Group performance status of 1 or less with three or more previous lines of therapy, or were double refractory to a proteasome inhibitor and immunomodulatory drug, and had received a proteasome inhibitor, immunomodulatory drug, and anti-CD38 antibody. A single cilta-cel infusion (target dose 0 75 10 6 CAR + T cells per kg) was administered 5-7 days after lymphodepletion. Patient-reported outcomes were assessed using the European Organisation for Research and Treatment of Cancer (EORTC) quality of life questionnaire core 30-item, pre-specified items from the EORTC myeloma module, and EuroQol five-dimensional descriptive system questionnaire. Clinically meaningful changes in patient-reported outcomes were defined by anchor-based minimally important differences. This trial is registered with ClinicalTrials.gov, NCT03548207. This trial is completed but feeding into a long-term follow-up study. FINDINGS: Between July 16, 2018, and Oct 7, 2019, 78 patients were enrolled and underwent apheresis in phase 2 of the study. 68 patients were treated (43 [63%] male, 49 [72%] White), and their patient-reported outcomes assessed (median follow-up 16 9 months, IQR 15 7-17 5). After infusion, a transient decline was observed, followed by improvements in global health status (mean change from baseline to day 464 +8 0 points, SD 20 9), physical (+4 6 points, 21 1), and emotional functional scales (+1 9 points, 23 7) over time, and declines for symptom-based scores (-14 1 pain, SD 31 5 and -15 4 fatigue; SD 29 5), indicating improved patient HRQOL following treatment with cilta-cel. INTERPRETATION: These durable HRQOL improvements are consistent with clinical findings, in which a single cilta-cel infusion led to substantial and durable responses in heavily pre-treated patients with relapsed or refractory multiple myeloma. These results support the use of cilta-cel in patients with relapsed or refractory multiple myeloma. FUNDING: Janssen Research & Development and Legend Biotech USA.
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