CD81 通过阻断 CD274/PD-L1 的选择性自噬降解驱动放射抵抗性胶质母细胞瘤的免疫逃逸
CD81 drives immune evasion in radioresistant glioblastoma by blocking selective autophagic degradation of CD274/PD-L1.
CELL INTELLIGENCE · 肿瘤细胞治疗研究
肿瘤细胞治疗研究
英文原题:The clinical utility of autologous tumor lysate-loaded dendritic cell vaccination for patients with glioma: A systematic review and meta-analysis.
The clinical utility of autologous tumor lysate-loaded dendritic cell vaccination for patients with glioma: A systematic review and meta-analysis.
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在胶质瘤中,DC 疫苗显示出暂时性的疗效;疾病稳定比消退更为常见。影响倾向于降低对早期疾病的抵抗性。提高疗效仍然至关重要。通过适当的辅助治疗整合,可以增强早期治疗的效果。
树突状细胞(DC)疫苗在胶质瘤治疗中显示出前景,但最佳使用方式仍不确定。本meta分析考察了DC疫苗对胶质瘤的疗效和安全性。
本系统综述和meta分析研究按照系统综述和meta分析首选报告项目进行。从建库至2023年10月23日,对电子数据库PubMed、Embase、Web of Science和Scopus进行了全面评估。
共纳入12项研究,998例患者,平均年龄范围为40.2至56岁。在12篇文章中,DC疫苗6个月总生存期(OS)为100%[95%置信区间{95%CI}:100%-100%]。12个月OS分别为75%[95%CI:65%-85%],但24个月OS下降至32%[95%CI:20%-43%]。6个月和12个月无进展生存期分别达到49%[95%CI:21%-77%]和19%[95%CI:8%-30%]。对影像学结局的研究显示,完全缓解率和部分缓解率分别为13%[95%CI:17%-42%]和26%[95%CI:10%-42%],尽管疾病稳定达到33%[95%CI:15%-51%],提示以抗肿瘤作用为主。疾病进展率也为24%[95%CI:9%-57%]。
Dendritic cell (DC) vaccines show promise for glioma treatment, but optimal use remains uncertain. This meta-analysis examined DC vaccine efficacy and safety for gliomas.
This systematic review and meta-analysis study was conducted using the Preferred Reporting Items for Systematic Reviews and Meta-Analyses. From the date of inception to October 23, 2023, electronic databases PubMed, Embase, Web of Science, and Scopus have been thoroughly evaluated.
A total of 12 studies with 998 patients and a mean age ranging from 40.2 to 56 years were included. Across 12 articles, DC vaccine 6-month overall survival (OS) was 100% [95% confidence interval {95%CI}: 100%-100%]. Respectively, 12-month OS reported 75% [95%CI: 65%-85%] but declined to 32% [95%CI: 20%-43%] for 24-month OS. 6- and 12-month progression-free survival reached 49% [95%CI: 21%-77%] and 19% [95%CI:8%-30%]. Studying radiological outcomes shows that complete response and partial response rates were 13% [95%CI: 17%-42%], and 26% [95%CI: 10%-42%], though stable disease reached 33% [95%CI: 15%-51%], suggesting predominant antineoplastic effects. The progressive disease rate also was 24% [95%CI: 9%-57%].
In gliomas, DC vaccinations show a temporary efficacy; stability is more prevalent than regression. Impacts favor decreased resistance to early disease. Enhancing efficacy remains critical. Early therapy can be enhanced by appropriate supplementary therapy integration.
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