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:Adjuvant Vaccination with Allogenic Dendritic Cells Significantly Prolongs Overall Survival in High-Grade Gliomas: Results of a Phase II Trial.
Adjuvant Vaccination with Allogenic Dendritic Cells Significantly Prolongs Overall Survival in High-Grade Gliomas: Results of a Phase II Trial.
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近年来,癌症治疗中的免疫疗法受到了越来越多的关注。最近,我们团队报告了一例胶质母细胞瘤患者,在接受基于树突状细胞的疫苗接种后,出现了强烈的Th1免疫反应,并几乎实现了肿瘤完全缓解。
在此,我们报告了一项I/II期前瞻性、非对照临床试验的结果,该试验纳入了37名患有胶质母细胞瘤或4级星形细胞瘤的患者。在手术后首次复发时,患者开始每月接受同种异体DC-自体肿瘤细胞杂交瘤的皮内注射。前瞻性评估了总生存期、生活质量及免疫学特征。与基因组数据共享数据库中的患者相比,接种疫苗的胶质母细胞瘤患者的总生存期为27.6±2.4个月(对比16.3±0.7,log-rank p<0.001,风险比0.53,95%CI 0.36-0.78,p<0.01),而接种疫苗的4级星形细胞瘤患者的总生存期为59.5±15.9个月(对比19.8±2.5,log-rank p<0.05,风险比0.18,95%CI 0.05-0.62,p<0.01)。
此外,截至本报告时,有七名接种疫苗的患者(两名IDH-1突变型和五名野生型)仍然存活(自诊断以来总生存期为47.9个月,标准差21.1,范围:25.4-78.6个月;自复发以来为34.2个月,范围:17.8至40.7,标准差21.3)。
我们相信,此处报告的数据能够促进基于细胞免疫疗法的高级别胶质瘤治疗方案的改进。
Immunotherapy for cancer treatment has gained increased attention in recent years. Recently, our group reported the case of a patient with glioblastoma who underwent vaccination based on dendritic cells and experienced a strong Th1 immune response together with near-complete tumor remission.
Here we report the results of a phase I/II prospective, non-controlled clinical trial with 37 patients harboring glioblastoma or grade 4 astrocytomas. At the time of first recurrence after surgery, patients began receiving monthly intradermal injections of allogenic DC-autologous tumor cell hybridomas.
Overall survival, quality of life, and immunological profiles were assessed prospectively. Compared with patients in the Genomic Data Commons data bank, overall survival for vaccinated patients with glioblastoma was 27. 6 ± 2. 4 months (vs. 16. 3 ± 0. 7, log-rank p < 0. 001, hazard ratio 0. 53, 95%CI 0. 36-0. 78, p < 0. 01), and it was 59. 5 ± 15. 9 for vaccinated astrocytoma grade 4 patients (vs. 19. 8 ± 2. 5, log-rank p < 0. 05, hazard ratio 0. 18, 95%CI 0. 05-0. 62, p < 0. 01).
Furthermore, seven vaccinated patients (two IDH-1-mutated and five wild type) remain alive at the time of this report (overall survival 47. 9 months, SD 21. 1, range: 25. 4-78. 6 months since diagnosis; and 34. 2 months since recurrence, range: 17. 8 to 40. 7, SD 21. 3).
We believe that the data reported here can foster the improvement of treatment protocols for high-grade gliomas based on cellular immunotherapy.
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