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:Advancements and challenges: immunotherapy therapy in high-grade glioma - a meta-analysis of randomized clinical trials.
Advancements and challenges: immunotherapy therapy in high-grade glioma - a meta-analysis of randomized clinical trials.
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免疫治疗有望成为 HGG 的有效治疗方法,尤其是 DCV。然而,结果因治疗类型和患者个体特征的不同而差异显著。需要进一步的随机对照试验来建立可靠的临床指南并优化治疗方案。
高级别胶质瘤(HGG)是最具侵袭性的原发性脑肿瘤,尽管采用常规治疗,预后仍然很差。免疫治疗因其能够激发针对肿瘤细胞的靶向免疫反应,已成为一种有前景的治疗途径。
本meta分析旨在评估多种免疫治疗策略,包括免疫检查点抑制剂(ICI)、病毒疗法和树突状细胞疫苗(DCV)在治疗HGG中的疗效和安全性。
按照PRISMA框架,我们检索了PubMed、Cochrane和Embase中报告HGG患者接受免疫治疗结局的研究。关键指标包括总生存期、无进展生存期和治疗相关不良事件。
我们回顾了47项研究,分析了3674例接受免疫治疗的HGG患者数据。接受ICI治疗的患者平均总生存期为11.05个月,病毒治疗为11.79个月,而DCV显著更长,为24.11个月。ICI的平均无进展生存期(PFS)为3.65个月。病毒治疗显示PFS有利于对照组,表明影响极小,而DCV显示出显著的PFS改善,与对照组相比,中位风险比低0.43倍(95% CI:29-64%)。ICI的不良事件主要为1级或2级,病毒治疗包括一例5级事件,DCV的不良事件主要为1级或2级,表明安全性良好。
High-grade gliomas (HGG) are the most aggressive primary brain tumors with poor prognoses despite conventional treatments. Immunotherapy has emerged as a promising avenue due to its potential to elicit a targeted immune response against tumor cells.
This meta-analysis aimed to evaluate the efficacy and safety of various immunotherapeutic strategies, including immune checkpoint inhibitors (ICI), virotherapy, and dendritic cell vaccines (DCV) in treating HGG.
Following the PRISMA framework, we searched PubMed, Cochrane, and Embase for studies reporting outcomes of HGG patients treated with immunotherapy. Key metrics included overall survival, progression-free survival, and treatment-related adverse events.
We reviewed 47 studies, analyzing data from 3674 HGG patients treated with immunotherapy. The mean overall survival for patients treated with ICI was 11.05 months, with virotherapy at 11.79 months and notably longer for DCV at 24.11 months. The mean progression-free survival (PFS) for ICIs was 3.65 months. Virotherapy demonstrated a PFS favoring the control group, indicating minimal impact, while DCV showed substantial PFS improvement with a median of 0.43 times lower hazard compared to controls (95% CI: 29-64%). Adverse events were primarily Grade 1 or 2 for ICI, included a Grade 5 event for virotherapy, and were predominantly Grade 1 or 2 for DCV, indicating a favorable safety profile.
Immunotherapy holds potential as an effective treatment for HGG, especially DCV. However, results vary significantly with the type of therapy and individual patient profiles. Further randomized controlled trials are necessary to establish robust clinical guidelines and optimize treatment protocols.
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