决定异体 CAR T 细胞排斥与扩增的细胞和分子机制
Cellular and molecular mechanisms determining allogeneic CAR T cell rejection and expansion.
英文原题:Cross-study safety analysis of risk factors in CAR T cell clinical trials: An FDA database pilot project.
Cross-study safety analysis of risk factors in CAR T cell clinical trials: An FDA database pilot project.
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嵌合抗原受体(CAR)T细胞安全性数据库项目探索跨研究安全性数据的应用,以识别CAR-T 输注后严重细胞因子释放综合征(sCRS)和严重神经毒性(sNTX)的相关风险因素。赞助方自愿提交了17项Ⅰ/Ⅱ期研究共1926名受试者的数据,包括6项急性淋巴细胞白血病(ALL)、5项非霍奇金淋巴瘤(NHL)和6项多发性骨髓瘤(MM)研究。与NHL或MM受试者相比,ALL受试者发生sCRS和sNTX的风险较高。与使用数据库中其他载体设计制备的产品相比,接受含CD28序列的γ-逆转录病毒载体制备CAR-T 产品者,sNTX发生率更高。在较低毒性分级时使用细胞因子靶向治疗和糖皮质激素,与sCRS发生率较低相关。尽管本探索性研究受限于跨研究比较未作调整,但独立重现了CAR-T 毒性的已知风险因素。研究结果为CAR-T 临床开发领域利益相关者提供安全性趋势信息,可用于早期临床试验设计,也为进一步研究提供方向。
The Chimeric Antigen Receptor (CAR) T Cell Safety Database Project explored the use of cross-study safety data to identify risk factors associated with severe cytokine release syndrome (sCRS) and severe neurological toxicities (sNTX) after CAR T cell administration. Sponsors voluntarily submitted data for 1,926 subjects from 17 phases 1 and 2 studies (six acute lymphocytic leukemia [ALL], five non-Hodgkin's lymphoma [NHL], and six multiple myeloma [MM] studies). Subjects with ALL had a higher risk for developing sCRS and sNTX compared with subjects with NHL or MM.
Subjects who received CAR T cells produced with gammaretrovirus vectors including CD28 sequences had higher rates of sNTX compared with subjects who received products produced with other vector designs included in the database. Use of cytokine-directed therapies and corticosteroids at lower toxicity grades were associated with lower rates of sCRS.
Although this exploratory study was limited by unadjusted cross-study comparisons, it independently reproduced known risk factors for CAR T cell toxicity. Findings provide stakeholders in the CAR T cell clinical development community information on safety trends for consideration in early phase clinical trial design, as well as avenues for additional research.
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