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:Efficacy and safety of innate and adaptive immunotherapy combined with standard of care in high-grade gliomas: a systematic review and meta-analysis.
Efficacy and safety of innate and adaptive immunotherapy combined with standard of care in high-grade gliomas: a systematic review and meta-analysis.
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因此,DC 疫苗显著延长了 HGG 患者的 OS,但 VT 和 IP 的疗效仍需进一步研究探索。所评估的所有治疗方案均与某些副作用相关。
恶性胶质瘤是最常见的颅内恶性肿瘤,死亡率最高。在免疫治疗时代,确定哪种类型的免疫治疗能提供最佳的生存机会非常重要。
在此,通过系统评价和meta分析评估了免疫治疗在高级别胶质瘤(HGG)中的疗效和安全性。探讨了不同类型免疫治疗之间的差异。检索到的命中结果在2,317篇文章中筛选纳入。我们提取了总生存期(OS)和无进展生存期(PFS)的风险比(HR)作为检验免疫治疗疗效的两个关键结局。我们还分析了所报告相应不良事件的数据,以评估免疫治疗的安全性。本研究已在PROSPERO注册(CRD42019112356)。
我们共纳入1,271例患者,其中524例接受了免疫治疗联合标准治疗(SOC),747例仅接受SOC。我们发现免疫治疗延长了OS(HR = 0.74;95% CI,0.56-0.99;Z = -2.00,P = 0.0458 < 0.05)和PFS(HR = 0.67;95% CI,0.45-0.99;Z = -1.99,P = 0.0466 < 0.05),尽管出现了一些不良事件(比例 = 0.0773,95% CI,0.0589-0.1014)。我们的数据证明了树突状细胞(DC)疫苗在延长胶质瘤患者OS方面的疗效(HR = 0.38;95% CI,0.21-0.68;Z = -3.23;P = 0.0012 < 0.05)。溶瘤病毒治疗(VT)仅在亚组分析中延长了患者生存期(HR = 0.60;95% CI,0.45-0.80;Z = -3.53;P = 0.0004 < 0.05)。相比之下,免疫增强(IP)未延长OS(HR = 0.69;95% CI,0.50-0.96;Z = -2.23;P = 0.0256)。
Malignant glioma is the most common intracranial malignant tumor with the highest mortality. In the era of immunotherapy, it is important to determine what type of immunotherapy provides the best chance of survival. METHOD: Here, the efficacy and safety of immunotherapy in high-grade glioma (HGG) were evaluated by systematic review and meta-analysis. The differences between various types of immunotherapy were explored. Retrieved hits were screened for inclusion in 2,317 articles. We extracted the overall survival (OS) and progression-free survival (PFS) hazard ratios (HRs) as two key outcomes for examining the efficacy of immunotherapy. We also analyzed data on the reported corresponding adverse events to assess the safety of immunotherapy. This study was registered with PROSPERO (CRD42019112356).
We included a total of 1,271 patients, of which 524 received a combination of immunotherapy and standard of care (SOC), while 747 received SOC alone. We found that immunotherapy extended the OS (HR = 0.74; 95% confidence interval [CI], 0.56-0.99; Z = -2.00, P = 0.0458 < 0.05) and PFS (HR = 0.67; 95% CI, 0.45-0.99; Z = -1.99, P = 0.0466 < 0.05), although certain adverse events occurred (proportion = 0.0773, 95% CI, 0.0589-0.1014). Our data have demonstrated the efficacy of the dendritic cell (DC) vaccine in prolonging the OS (HR = 0.38; 95% CI, 0.21-0.68; Z = -3.23; P = 0.0012 < 0.05) of glioma patients. Oncolytic viral therapy (VT) only extended patient survival in a subgroup analysis (HR = 0.60; 95% CI, 0.45-0.80; Z = -3.53; P = 0.0004 < 0.05). By contrast, immunopotentiation (IP) did not prolong OS (HR = 0.69; 95% CI, 0.50-0.96; Z = -2.23; P = 0.0256).
Thus, DC vaccination significantly prolonged the OS of HGG patients, however, the efficacy of VT and IP should be explored in further studies. All the therapeutic schemes evaluated were associated with certain side effects. SYSTEMATIC REVIEW REGISTRATION: https://www.crd.york.ac.uk/PROSPERO/display_record.php?RecordID=112356.
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