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:Predicting CAR-T outcomes in R/R DLBCL: a multicenter real-world study of a 5-index model.
Predicting CAR-T outcomes in R/R DLBCL: a multicenter real-world study of a 5-index model.
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该 5 指标风险模型在真实世界环境中展现出稳健的预测能力,为中国接受 CAR-T 治疗的弥漫大 B 细胞淋巴瘤患者的个体化治疗决策提供了可靠依据。
这项多中心回顾性真实世界研究旨在验证既往开发的CD19 CAR-T 疗效预测模型在中国R/R DLBCL患者中的表现。纳入2021年8月1日至2024年11月30日期间在中国4个中心接受CD19 CAR-T 治疗的92例DLBCL患者。采用5项指标预测模型——纳入双表达淋巴瘤状态、TP53改变、ECOG体能状态评分≥2、肿块≥5 cm以及既往治疗线数≥4——预测治疗结局。主要终点为总缓解率(ORR)、完全缓解(CR)率、无进展生存期(PFS)和总生存期(OS)。
中位随访时间为14.6个月。5项指标模型的C指数为0.767,提示预测性能良好。该模型能有效将患者分为不同风险组,各组PFS(P<0.0001)和OS(P=0.0007)差异显著。其表现优于IPI和R-IPI等传统预后指标。 讨论:该5项指标风险模型在真实世界环境中显示出稳健的预测能力,可为接受CAR-T 治疗的中国DLBCL患者个体化治疗决策提供可靠依据。未来将进一步优化模型并开展多区域验证。
This multicenter retrospective real world study aimed to validate a previously developed efficacy prediction model for CD19 CAR T in Chinese patients with R/R DLBCL. A total of 92 patients with DLBCL who received CD19 CAR T across four Chinese centers from August 1, 2021, to November 30, 2024 were included. The 5 index prediction model (incorporating double expressor lymphoma status, TP53 alterations, ECOG performance status 2, bulky disease 5 cm, and prior therapy lines 4) was applied to predict treatment outcomes. The primary endpoints were overall response rate (ORR), complete response (CR) rate, progression free survival (PFS), and overall survival (OS).
The median follow up was 14.6 months. The C index for the 5 index model was 0.767, indicating good predictive performance. The model effectively stratified patients into different risk groups, with significant differences observed in PFS (P < 0.0001) and OS (P = 0.0007) across groups. The model outperformed traditional prognostic indices such as IPI and R IPI. DISCUSSION: The 5 index risk model demonstrated robust predictive ability in a real world setting, providing a reliable basis for personalized treatment decisions in Chinese DLBCL patients undergoing CAR T. Future work will focus on further optimizing the model and conducting multi regional validation.
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