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.
我们评估了11例接受单一批次cemacabtagene ansegedleucel(cema-cel)治疗的大B细胞淋巴瘤患者,cemacabtagene ansegedleucel是一种异体抗CD19 CAR T产品。
英文原题:Factors Associated with Immune Effector Cell-Associated Neurotoxicity Syndrome in Adults with Hematological Malignancies Undergoing Chimeric Antigen Receptor T-Cell Therapy: A Systematic Review.
大约一半接受CAR T治疗的血液病患者会发生ICANS。尽管某些因素可能促进ICANS的发生,但研究及样本有限、多数研究为回顾性设计以及结果之间的不一致性,使得无法得出明确的风险因素结论。对护理实践的启示:护士在治疗后监测中发挥着关键作用,能够早期发现和管理ICANS,因为他们与患者直接且持续接触。提高护士对ICANS潜在风险因素的认识,可以增强其管理该病症的警觉性和有效性。
我们系统评价了探讨成人血液系统恶性肿瘤患者接受CAR-T细胞治疗后ICANS发生相关因素的研究,并估算了ICANS的患病率。
我们按照PRISMA指南,在4个数据库中对2010年至2024年12月发表的研究进行了系统综述(SR)。我们使用精确二项分布和基于评分检验的95%置信区间估计ICANS患病率。我们应用Freeman-Tukey双重反正弦变换,使用Stata中的Metaprop命令在随机效应模型内稳定方差。
本SR纳入16项研究(14项回顾性研究,n = 135;2项前瞻性研究,n = 300)。样本包括接受抗CD19和抗BCMA治疗的多种血液系统恶性肿瘤成人患者。一些临床因素似乎与ICANS的发生率和严重程度相关。在回顾性研究中,所有级别ICANS的合并患病率为41%(95% CI:31%-51%),3级ICANS为20%(95% CI:13%-28%)。在前瞻性研究中,合并患病率为51%(95% CI:45%-56%)。
OBJECTIVES: We systematically appraised studies investigating factors associated with ICANS development after CAR-T cell therapies in adults with hematological malignancies and estimated ICANS prevalence. METHOD: We conducted a systematic review (SR) in 4 databases following the PRISMA (Preferred Reporting Items for Systematic Reviews and Meta-Analyses) guidelines for studies published from 2010 to December 2024. We estimated ICANS prevalence with exact binomial and score test-based 95% confidence intervals. We applied the Freeman-Tukey double arcsine transformation to stabilize variances within random-effects models using the Metaprop command in Stata. RESULTS: Sixteen studies (14 retrospective, n = 135, and 2 prospective, n = 300) were included in this SR. The sample comprised adults with various hematological malignancies who received anti-CD19 anti-BCMA. Some clinical factors seem to be associated with ICANS incidence and severity. In retrospective studies, the pooled prevalence was 41% (95% CI: 31%-51%) for all grades of ICANS and 20% (95% CI: 13%-28%) for grade 3 ICANS. In prospective studies, the pooled prevalence was 51% (95% CI: 45%-56%). CONCLUSIONS: Approximately half of hematological patients undergoing CAR T therapy develop ICANS. Although some factors may contribute to the development of ICANS, limited studies and samples, the retrospective nature of the majority of studies, and the discordance among the results preclude certain risk factors conclusions. IMPLICATIONS FOR NURSING PRACTICE: Nurses play a pivotal role in post-treatment monitoring in the early detection and management of ICANS, given their direct and continuous patient interaction. Increasing nurses' awareness of potential risk factors for ICANS can enhance their vigilance and effectiveness in managing this condition.
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