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lisocabtagene maraleucel 在复发/难治性大 B 细胞淋巴瘤中的体内细胞扩增及其与疗效和安全性的关联

英文原题:In Vivo Cellular Expansion of Lisocabtagene Maraleucel and Association With Efficacy and Safety in Relapsed/Refractory Large B-Cell Lymphoma.

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In Vivo Cellular Expansion of Lisocabtagene Maraleucel and Association With Efficacy and Safety in Relapsed/Refractory Large B-Cell Lymphoma.

PubMed 2022/03/20(内容时间) Clin Pharmacol Ther Q1 · IF 4.9(JCR 2025)

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中文摘要

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。

展开英文摘要原文

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.

论文信息

作者
Ogasawara K、Lymp J、Mack T、Dell'Aringa J、Huang CP、Smith J、Peiser L、Kostic A
第一作者单位
Bristol Myers Squibb, Princeton, New Jersey, USA.United Kingdom
通讯作者单位
Bristol Myers Squibb, Seattle, Washington, USA.United Kingdom
文献类型
非美国政府资助研究
期刊
Clinical pharmacology and therapeutics2022 Jul
原文标识
PubMed 35156195 · DOI 10.1002/cpt.2561