CAR-T(CAR-T)细胞疗法在非肿瘤性疾病中的应用
Chimeric antigen receptor T (CAR-T) cell therapy in non-oncological diseases.
CAR-T(CAR-T)细胞在血液系统恶性肿瘤中的应用推动了这种免疫治疗形式的显著进展。
CELL INTELLIGENCE · 肿瘤细胞治疗研究
肿瘤细胞治疗研究
英文原题:The Dutch CAR-T Tumorboard Experience: Population-Based Real-World Data on Patients with Relapsed or Refractory Large B-Cell Lymphoma Referred for CD19-Directed CAR T-Cell Therapy in The Netherlands.
The Dutch CAR-T Tumorboard Experience: Population-Based Real-World Data on Patients with Relapsed or Refractory Large B-Cell Lymphoma Referred for CD19-Directed CAR T-Cell Therapy in The Netherlands.
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不同国家的复发/难治性(R/R)大 B 细胞淋巴瘤(LBCL)患者接受CAR-T(CAR-T)细胞治疗的真实世界结局差异显著。荷兰 CAR-T 肿瘤委员会建立了独特的全国基础设施,负责转诊、治疗资格评估和数据收集。
本研究旨在评估荷兰人群中 axicabtagene ciloleucel(axi-cel)的真实世界结局,包括迄今报道较少的健康相关生活质量(HR-QoL)影响。纳入 2020 年 5 月至 2022 年 5 月期间接受 2 线全身治疗后转诊接受 axi-cel 的全部 R/R LBCL 患者(N = 250)。160 例患者接受单采,其中 145 例接受 axi-cel 输注。主要不符合治疗资格的原因是疾病快速进展。治疗结局优于或至少与其他研究相当:最佳总体缓解率为 84%(完全缓解率 66%);12 个月无进展生存率和总生存率分别为 48% 和 62%。12 个月非复发死亡率(NRM)为 5%,主要由感染导致。从治疗后第 9 个月起,多个 HR-QoL 领域出现具有临床意义的改善。专家指导的患者筛选有助于 CAR-T 治疗有效且可持续地应用。队列之间的匹配比较有助于理解不同国家治疗结局差异并选择最佳实践。尽管结果良好,相当比例的 R/R LBCL 患者仍存在未满足的医疗需求。
The real-world results of chimeric antigen receptor T-cell (CAR-T) therapy for patients with relapsed/refractory (R/R) large B-cell lymphoma (LBCL) substantially differ across countries. In the Netherlands, the CAR-T tumorboard facilitates a unique nationwide infrastructure for referral, eligibility assessment and data collection. The aim of this study was to evaluate real-world outcomes of axicabtagene ciloleucel (axi-cel) in the Dutch population, including the thus-far underreported effects on health-related quality of life (HR-QoL). All patients with R/R LBCL after 2 lines of systemic therapy referred for axi-cel treatment between May 2020-May 2022 were included (N = 250). Of the 160 apheresed patients, 145 patients received an axi-cel infusion.
The main reason for ineligibility was rapidly progressive disease. The outcomes are better or at least comparable to other studies (best overall response rate: 84% (complete response: 66%); 12-month progression-free-survival rate and overall survival rate: 48% and 62%, respectively). The 12-month NRM was 5%, mainly caused by infections. Clinically meaningful improvement in several HR-QoL domains was observed from Month 9 onwards.
Expert-directed patient selection can support effective and sustainable application of CAR-T treatment. Matched comparisons between cohorts will help to understand the differences in outcomes across countries and select best practices. Despite the favorable results, for a considerable proportion of patients with R/R LBCL there still is an unmet medical need.
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