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.
CELL INTELLIGENCE · 肿瘤细胞治疗研究
肿瘤细胞治疗研究
英文原题:In Vivo Cellular Expansion of Lisocabtagene Maraleucel and Association With Efficacy and Safety in Relapsed/Refractory Large B-Cell Lymphoma.
In Vivo Cellular Expansion of Lisocabtagene Maraleucel and Association With Efficacy and Safety in Relapsed/Refractory Large B-Cell Lymphoma.
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Lisocabtagene maraleucel(liso-cel)是一种自体、靶向 CD19 的CAR-T 细胞产品,用于治疗接受过 2 线或以上系统性治疗后复发/难治性大 B 细胞淋巴瘤(LBCL)的成人患者。单次给药 liso-cel 后的体内细胞扩增特征已被描述。本文进一步表征了关键研究 TRANSCEND NHL 001(ClinicalTrials.gov 标识符,NCT02631044)中 liso-cel 的体内扩增,以评估在调整关键基线特征后,单次给药 liso-cel 后的体内细胞扩增与疗效或安全性之间的关系。采用两种生物分析方法,即定量聚合酶链反应和流式细胞术,评估 liso-cel 的细胞动力学,二者在体内细胞扩增方面显示出高度一致性。多变量 logistic 回归分析表明,在复发/难治性 LBCL 患者中,liso-cel 较高的体内细胞扩增与较高的总缓解率和完全缓解率相关,并与较高的细胞因子释放综合征和神经系统事件发生率相关。年龄和肿瘤负荷(按垂直直径乘积之和计算)可能混杂了 liso-cel 体内细胞扩增与疗效之间的关系,在控制这些因素后,该关联变得更强。
该研究测试了 liso-cel 的重复给药;然而,重复给药后的 liso-cel 体内细胞扩增低于初始给药后。这些发现应有助于全面理解 liso-cel 的体内细胞动力学及其与复发/难治性 LBCL 结局的关联。
Lisocabtagene maraleucel (liso-cel) is an autologous, CD19-directed, chimeric antigen receptor T-cell product for the treatment of adult patients with relapsed or refractory large B-cell lymphoma (LBCL) after 2 or more lines of systemic therapy. In vivo cellular expansion after single-dose administration of liso-cel has been characterized. In this article, in vivo liso-cel expansion in the pivotal study TRANSCEND NHL 001 (ClinicalTrials. gov identifier, NCT02631044) was further characterized to assess the relationship between in vivo cellular expansion after single-dose administration of liso-cel and efficacy or safety after adjusting for key baseline characteristics. Two bioanalytical methods, quantitative polymerase chain reaction and flow cytometry, were used for the assessment of cellular kinetics of liso-cel, which showed high concordance for in vivo cellular expansion.
Multivariable logistic regression analyses demonstrated that higher in vivo cellular expansion of liso-cel was associated with a higher overall response and complete response rate, and a higher incidence of cytokine release syndrome and neurological events in patients with relapsed or refractory LBCL.
Age and tumor burden (by sum of the product of perpendicular diameters) were likely to confound the relationship between in vivo cellular expansion and efficacy, where the association became stronger after controlling for these factors. Repeat dosing of liso-cel was tested in the study; however, in vivo cellular expansion of liso-cel was lower after repeat dosing than after the initial dose.
These findings should enable a comprehensive understanding of the in vivo cellular kinetics of liso-cel and the association with outcomes in relapsed/refractory LBCL.
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