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:Outcomes of relapsed/refractory diffuse large B-cell lymphoma and influence of chimaeric antigen receptor T trial eligibility criteria in second line-A population-based study of 736 patients.
Outcomes of relapsed/refractory diffuse large B-cell lymphoma and influence of chimaeric antigen receptor T trial eligibility criteria in second line-A population-based study of 736 patients.
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近期发表的几项试验探讨了复发/难治性弥漫性大B细胞淋巴瘤(R/R DLBCL)的新型疗法。为评估这些疗法在真实世界中的获益,需要关于临床常规治疗患者的全面数据。
我们报告了2007-2014年期间瑞典所有接受治愈性治疗的DLBCL患者中识别出的736例R/R DLBCL患者的结局。评估了生存率及其与疾病特征、二线治疗和是否符合嵌合抗原受体(CAR)T细胞试验标准的关联。中位总生存期(OS)为6.6个月(≤70岁为9.6个月,>70岁为4.9个月)。早期复发(≤12个月)与选择较低强度治疗和较差生存率密切相关。在年龄不超过70岁的患者中,63%开始接受强化二线治疗,34%接受了自体干细胞移植(ASCT)。移植患者的两年OS为56%(早期复发≤12个月为40%,晚期复发>12个月为66%)。少数患者≤76岁(n = 178/506,35%)符合CAR-T 试验标准。符合试验标准的早期复发患者的中位无进展生存期(PFS)为4.8个月。
总之,大多数R/R DLBCL表现为早期复发,且往往不符合或无法完成强化方案,导致生存结局不佳。符合CAR-T 试验条件的真实世界患者同样预后不良,这为新型疗法的疗效提供了基准。
Several recently published trials investigate novel therapies for relapsed/refractory diffuse large B-cell lymphoma (R/R DLBCL). To estimate the benefit of these therapies in the real-world setting, comprehensive data on patients treated in clinical routine are needed.
We report outcomes for 736 R/R DLBCL patients identified among all curatively treated DLBCL patients in Sweden in the period 2007-2014. Survival and associations with disease characteristics, second-line treatment and fulfilment of chimaeric antigen receptor (CAR) T-cell trial criteria were assessed. Median overall survival (OS) was 6. 6 months ( 70 years 9. 6 months, >70 years 4. 9 months). Early relapse ( 12 months) was strongly associated with selection of less intensive treatment and poor survival.
Among patients of at most 70 years of age, 63% started intensive second-line treatment and 34% received autologous stem cell transplantation (ASCT). Two-year OS among transplanted patients was 56% (early relapse 12 months 40%, late relapse >12 months 66%). A minority of patients 76 years (n = 178/506, 35%) fitted CAR T trial criteria. Median progression-free survival (PFS) for patients with early relapse fitting trial criteria was 4. 8 months.
In conclusion, most R/R DLBCL manifest early and are often ineligible for or cannot complete intensive regimens resulting in dismal survival. Real-world patients eligible for CAR T trials also did poorly, providing a benchmark for efficacy of novel therapies.
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