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:Assessment of treatment response to dendritic cell vaccine in patients with glioblastoma using a multiparametric MRI-based prediction model.
Assessment of treatment response to dendritic cell vaccine in patients with glioblastoma using a multiparametric MRI-based prediction model.
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基于多参数 MRI 的预测模型可评估胶质母细胞瘤患者对 DCVax-L 的治疗反应。
自体肿瘤裂解物负载的树突状细胞疫苗(DCVax-L)是治疗胶质母细胞瘤的一种有前景的治疗方式。本研究的目的是探讨基于多参数MRI的预测模型在评估接受DCVax-L治疗的胶质母细胞瘤患者治疗反应中的潜在效用。
纳入17例接受标准治疗+DCVax-L治疗的胶质母细胞瘤患者。当怀疑肿瘤进展(TP)并考虑再次手术时,我们试图以组织病理学/mRANO标准作为金标准,确定基于多参数MRI预测模型正确分类为TP+混合反应或假性进展(PsP)的病例数。多参数MRI模型由扩散和灌注MRI衍生参数计算得出的肿瘤进展预测概率(PP)组成。对接受标准治疗+DCVax-L治疗的患者与仅接受标准治疗的患者(外部对照)进行了总生存期(OS)比较。此外,采用Kaplan-Meier分析比较两组患者的OS,以PsP、Ki-67和MGMT启动子甲基化状态作为分层变量。
多参数MRI模型正确预测了72.7%的病例(8/11)为TP + 混合反应,83.3%的病例(5/6)为PsP,与组织病理学/mRANO标准确定的最终诊断总体一致率为76.5%。PP值与组织病理学/mRANO标准之间存在显著的一致性相关系数(r = 0.54;p = 0.026)。DCVax-L治疗的患者OS显著长于接受标准治疗的患者(22.38 ± 12.8 vs. 13.8 ± 9.5个月,p = 0.040)。此外,伴有PsP的胶质母细胞瘤、MGMT启动子甲基化状态以及Ki-67值低于中位数的患者OS长于其对应组。
Autologous tumor lysate-loaded dendritic cell vaccine (DCVax-L) is a promising treatment modality for glioblastomas. The purpose of this study was to investigate the potential utility of multiparametric MRI-based prediction model in evaluating treatment response in glioblastoma patients treated with DCVax-L.
Seventeen glioblastoma patients treated with standard-of-care therapy + DCVax-L were included. When tumor progression (TP) was suspected and repeat surgery was being contemplated, we sought to ascertain the number of cases correctly classified as TP + mixed response or pseudoprogression (PsP) from multiparametric MRI-based prediction model using histopathology/mRANO criteria as ground truth. Multiparametric MRI model consisted of predictive probabilities (PP) of tumor progression computed from diffusion and perfusion MRI-derived parameters. A comparison of overall survival (OS) was performed between patients treated with standard-of-care therapy + DCVax-L and standard-of-care therapy alone (external controls). Additionally, Kaplan-Meier analyses were performed to compare OS between two groups of patients using PsP, Ki-67, and MGMT promoter methylation status as stratification variables.
Multiparametric MRI model correctly predicted TP + mixed response in 72.7% of cases (8/11) and PsP in 83.3% (5/6) with an overall concordance rate of 76.5% with final diagnosis as determined by histopathology/mRANO criteria. There was a significant concordant correlation coefficient between PP values and histopathology/mRANO criteria (r = 0.54; p = 0.026). DCVax-L-treated patients had significantly prolonged OS than those treated with standard-of-care therapy (22.38 ± 12.8 vs. 13.8 ± 9.5 months, p = 0.040). Additionally, glioblastomas with PsP, MGMT promoter methylation status, and Ki-67 values below median had longer OS than their counterparts.
Multiparametric MRI-based prediction model can assess treatment response to DCVax-L in patients with glioblastoma.
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