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:Prophylactic use of interleukin 6 monoclonal antibody can reduce CRS response of CAR-T cell therapy.
Prophylactic use of interleukin 6 monoclonal antibody can reduce CRS response of CAR-T cell therapy.
分数与星级只用于站内排序 —— 不代表疗效、安全性或个人适用性。
预防性使用 IL-6 单克隆抗体可显著降低 CAR-T 治疗后 CRS 并发症的发生率,也可降低 CAR-T 治疗后的 LDH 值和 CRP 峰值。
CAR-T(CAR-T)细胞免疫疗法正成为治疗血液系统恶性肿瘤最有前景的方法之一,然而,细胞因子释放综合征(CRS)等并发症严重威胁患者生命。白细胞介素6(IL-6)单克隆抗体是治疗CRS常用且有效的方法,然而,CAR-T 治疗前预防性使用IL-6单克隆抗体是否能降低CRS的发生率尚不清楚。
本研究旨在系统评价预防性使用IL-6单克隆抗体能否降低CRS的发生率。数据来源与方法:我们检索了PubMed、Embase、web of Science和Cochrane Library数据库,纳入截至2022年12月前报告的关于预防性使用IL-6单克隆抗体治疗CAR-T 细胞免疫治疗CRS相关并发症的研究。根据既定的纳入和排除标准筛选文献,提取相关数据,并使用Cochrane偏倚风险评估工具量表评价文献质量,使用Review Manager 5.3绘制相关图表。由于两项实验数据仅提供了中位数、最大值和最小值,均值和标准差(Standard Deviation,SD)由本文Delai计算,最终使用Review Manager进行数据处理,并使用STATA软件进行补充。
本研究共纳入2项试验,共37名参与者。Meta分析显示,与不使用IL-6单克隆抗体预防CRS相比,在CAR-T 细胞输注前1小时给予患者8 mg/kg的IL-6单克隆抗体,可降低CRS的发生率[RR: 0.41 95%置信区间(0.20, 0.86) I[2] = 0.0% P = 0.338 z = -2.369 (p = 0.018)]。在亚组分析中,与不使用IL-6单克隆抗体预防CRS相比,在CAR-T 细胞输注前1小时给予患者8 mg/kg的IL-6单克隆抗体,可降低乳酸脱氢酶(LDH)[MD: -617.21, 95%置信区间(-1104.41, -130.01) I[2] = 0% P = 0.88 Z = 2.48 (P = 0.01)],预防性使用IL-6单克隆抗体对降低CAR-T 治疗后C反应蛋白(CRP)峰值有显著效果[MD: -11.58, 95%置信区间(-15.28, -7.88) I[2] = 0.0% P = 0.73 z = 6.14 (p < 0.00001)]。
Chimeric antigen receptor T (CAR-T) cell immunotherapy is becoming one of the most promising treatments for hematological malignancies, however, complications such as cytokine release syndrome (CRS) seriously threaten the lives of patients. Interleukin 6(IL-6) monoclonal antibody is the common and useful treatment of CRS, however, it is not clear whether prophylactic use IL-6 monoclonal antibody before CAR-T therapy can reduce the incidence of CRS.
This study aims to systematically evaluate whether the prophylactic use of IL-6 monoclonal antibody can reduce the incidence of CRS. DATA SOURCES AND METHODS: We searched the PubMed, Embase, web of Science, and Cochrane Library databases for studies that reported the prophylactic use of IL-6 monoclonal antibody in the treatment of CRS-related complications of CAR-T cell immunotherapy before December 2022. The literature is screened according to the established inclusion and exclusion criteria, relevant data are extracted, and the quality of the literature is evaluated using the scale Cochrane bias risk assessment tool, and the Review Manager 5.3 is used to draw for related charts. Since the two experimental data only provide the median, the maximum and minimum values of the data, the mean and standard (Standard Deviation, SD) are calculated by this document Delai, and finally use Review Manager for data processing, and STATA software for supplementation.
A total of 2 trials with a total of 37 participants were included in this study. Meta-analysis showed that compared with no use of IL-6 monoclonal antibody to prevent CRS, IL-6 monoclonal antibody was given to patients at 8 mg/kg one hour before CAR-T cell infusion, which reduced the incidence of CRS [RR: 0.41 95% confidence interval (0.20, 0.86) I[2] = 0.0% P = 0.338 z = -2.369 ( p = 0.018)]. In subgroup analysis, compared with those who did not use IL-6 monoclonal antibody to prevent CRS, IL-6 monoclonal antibody was given to patients at 8 mg/kg one hour before CAR-T cell infusion, which reduced lactate dehydrogenase (LDH)[MD: -617.21, 95% confidence interval (-1104.41, -130.01) I[2] = 0% P = 0.88 Z = 2.48 ( P = 0.01)], prophylactic use of IL-6 monoclonal antibody has a significant effect on reducing peak C-reactive protein (CRP) after CAR-T therapy [MD: -11.58, 95% confidence interval (-15.28, -7.88) I[2] = 0.0% P = 0.73 z = 6.14 ( p < 0.00001)].
The prophylactic use of IL-6 monoclonal antibody can significantly reduce the incidence of CRS complications after CAR-T therapy, can also reduce LDH vaule and peak CRP vaule after CAR-T therapy. SYSTEMATIC REVIEW REGISTRATION: https://www.crd.york.ac.uk/prospero/display_record.php?ID=CRD42023487662, identifier CRD42023487662.
在 PubMed 查看 → 出版商原文(DOI) 全文 PDF(PMC)· 可下载 治疗专题与资料阅读指南 资料来源与翻译说明 报告译文或资料问题 →
MEMBER ACCOUNT
登录成功会直接打开下一页。