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:Chimeric antigen receptor-T cell therapy shows similar efficacy and toxicity in patients with diffuse large B-cell lymphoma aged 70 and older compared to younger patients: A multicenter cohort study.
Chimeric antigen receptor-T cell therapy shows similar efficacy and toxicity in patients with diffuse large B-cell lymphoma aged 70 and older compared to younger patients: A multicenter cohort study.
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靶向CD19的嵌合抗原受体(CAR)-T细胞疗法已成为复发/难治性弥漫性大B细胞淋巴瘤(r/r DLBCL)的标准治疗。尽管CAR-T 细胞治疗的获益在总体患者人群中已明确,但关于其在年龄≥70岁DLBCL患者(pts)中疗效和毒性的真实世界证据仍相对缺乏。
我们开展了一项多中心回顾性分析,纳入2019年至2023年间在三家三级医疗中心接受CAR-T 细胞治疗(axicabtagene ciloleucel或tisagenlecleucel)的172例r/r DLBCL患者。患者按CAR-T 输注时的年龄分组(<70岁 vs. ≥70岁)。随后进行了描述性和生存分析,包括倾向性评分匹配,以比较两个年龄组之间的结局。
我们识别出109例年龄<70岁和63例年龄≥70岁的患者。两个年龄组的总体缓解率相当(77.7% vs. 78.3%;p = 0.63)。中位随访时间为8.3个月,两个队列的中位无进展生存期分别为10.2个月(95%置信区间[CI]:6.5-21.8)和11.1个月(95% CI:4.9-NR)(p = 0.93)。中位总生存期分别达到21.8个月(95% CI:11.8-NR)和34.4个月(95% CI:10.1-NR)(p = 0.97)。未观察到细胞因子释放综合征(p = 0.53)或3级神经毒性(p = 0.56)的发生率存在显著差异。两组间的复发死亡率和非复发死亡率无显著差异。
我们的发现提供了额外支持,表明CAR-T 细胞疗法在年龄≥70岁的r/r DLBCL患者中可行且有效,其结局与在较年轻患者中观察到的结局相当。对于老年r/r DLBCL患者,不应放弃CAR-T 细胞治疗。
CD19-directed chimeric antigen receptor (CAR)-T cell therapy has become a standard treatment for relapsed/refractory diffuse large B-cell lymphoma (r/r DLBCL). While the benefits of CAR-T cell treatment are clear in the general patient population, there remains a relative scarcity of real-world evidence regarding its efficacy and toxicity in patients (pts) aged 70 years with DLBCL.
We conducted a multicenter retrospective analysis including 172 r/r DLBCL pts with CAR-T cell treatment, axicabtagene ciloleucel or tisagenlecleucel, between 2019 and 2023 at three tertiary centers. Pts were grouped by age at CAR-T infusion (<70 vs. 70 years). Subsequently, descriptive and survival analyses, including propensity score matching, were performed to compare outcomes between both age groups.
We identified 109 pts aged <70 and 63 pts aged 70 years. Overall response rates for both age groups were comparable (77. 7% vs. 78. 3%; p = 0. 63). With a median follow-up of 8. 3 months, median progression-free survival was 10. 2 months (95% confidence interval [CI]: 6. 5-21. 8) and 11. 1 months (95% CI: 4. 9-NR) ( p = 0. 93) for both cohorts.
Median overall survival reached 21. 8 months (95% CI: 11. 8-NR) and 34. 4 months (95% CI: 10. 1-NR) ( p = 0. 97), respectively. No significant differences in the incidence of cytokine release syndrome ( p = 0. 53) or grade 3 neurotoxicity ( p = 0. 56) were observed. Relapse and nonrelapse mortality were not significantly different between both groups.
Our findings provide additional support that CAR-T cell therapy is feasible and effective in patients with r/r DLBCL aged 70 years or older, demonstrating outcomes comparable to those observed in younger patients. CAR-T cell therapy should be not withheld for elderly patients with r/r DLBCL.
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