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 and factors influencing survival in patients with diffuse large B-cell lymphoma: a population-based analysis.
Outcomes and factors influencing survival in patients with diffuse large B-cell lymphoma: a population-based analysis.
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鉴于弥漫性大B细胞淋巴瘤(DLBCL)治疗格局的迅速演变,我们利用加拿大安大略省的关联行政数据集(ICES),在人群水平上对年龄≥18岁DLBCL患者的生存结局进行了当代分析。在8675例接受一线利妥昔单抗为基础治疗的患者中(中位年龄67岁;44%为女性),1675例(19%)接受了二线治疗(2L)。从2L开始的2年和5年总生存期(OS)分别为33%和26%。单因素分析显示,治愈性意向治疗(自体干细胞移植[ASCT])(占58%的患者)与姑息性放疗相比,OS更优(风险比[HR],0.56;P < .0001)。年龄≥60岁患者的OS劣于<60岁患者(60-69岁:HR,1.35;P =.0002;70-79岁:HR,1.64;P < .0001;≥80岁:HR,2.08;P < .0001)。
此外,早期复发与2年后复发的患者相比结局更差(<3个月:HR,1.45;P =.0002;3-6个月:HR,1.51;P =.0001;6-12个月:HR,1.88;P < .0001)。多因素分析在纳入乳酸脱氢酶、合并症负担、衰弱和收入因素后证实了这些关联。探索性分析表明,与2020年前接受姑息性治疗的历史队列相比,三线CAR-T 细胞治疗与结局改善相关(2年OS 56% vs 21%)。这项基于人群的分析表明,治愈性意向治疗(ASCT和CAR-T)与常规治疗方法相比,与OS改善相关。此处呈现的结局为未来旨在评估2L新型治疗对结局影响的分析提供了基准。
Given the rapidly evolving treatment landscape for diffuse large B-cell lymphoma (DLBCL), we performed a contemporary analysis of survival outcomes in patients aged 18 years with DLBCL at the population level using linked administrative data sets in Ontario, Canada (ICES). Among 8675 patients (median age, 67 years; 44% female) treated with frontline rituximab-based therapy, 1675 (19%) were treated with second-line therapy (2L).
The 2-year and 5-year overall survival (OS) from 2L were 33% and 26%, respectively. Univariate analysis demonstrated that curative-intent therapy (autologous stem cell transplantation [ASCT]) (58% of patients) was associated with better OS than palliative radiotherapy (hazard ratio [HR], 0. 56; P < . 0001). Patients aged 60 years showed inferior OS than those aged <60 years (age 60-69 years: HR, 1. 35; P =. 0002; aged 70-79 years: HR, 1. 64; P < . 0001; age 80 years: HR, 2. 08; P < . 0001).
In addition, early relapse was associated with worse outcomes than relapses occurring after 2 years (<3 months: HR, 1. 45; P =. 0002; 3-6 months: HR, 1. 51; P =. 0001; 6-12 months: HR, 1. 88; P < . 0001). Multivariable analysis confirmed these associations while accounting for lactate dehydrogenase, comorbidity burden, frailty, and income.
Exploratory analysis indicated that third-line chimeric antigen receptor T-cell (CAR-T) therapy was associated with improved outcomes compared to a historical cohort of patients treated with palliative therapy before 2020 (2-year OS 56% vs 21%). This population-based analysis suggests that curative-intent therapy (ASCT and CAR-T) is associated with improved OS over conventional treatment approaches. The outcomes presented here provide benchmarks for future analyses aimed at assessing the effects of novel treatments in the 2L on outcomes.
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