CELL INTELLIGENCE · 肿瘤细胞治疗研究
肿瘤细胞治疗研究
英文原题:Programmed death ligand 1 and tumor-infiltrating CD8(+) T lymphocytes are associated with the clinical features in meningioma.
Programmed death ligand 1 and tumor-infiltrating CD8(+) T lymphocytes are associated with the clinical features in meningioma.
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肿瘤体积与 PD-L1 表达相关,而 PTBE 是脑膜瘤中 CD8 + TIL 水平的独立预测因子。CD8 + TIL 水平与脑膜瘤肿瘤复发相关。
探讨脑膜瘤中程序性死亡配体-1(PD-L1)的表达和CD8+TIL(肿瘤浸润淋巴细胞)(TILs)的水平,并确定其水平与临床结局之间的关联。
我们进行了一项回顾性病例对照研究,纳入93例脑膜瘤患者。这些患者出现肿瘤复发,并在年龄、性别、入院时间、肿瘤部位、肿瘤体积、瘤周脑水肿(PTBE)、Simpson分级切除、WHO分级、术后放疗和随访时间方面与无复发的对照患者进行匹配。我们回顾了患者的临床资料,并进行免疫组化分析,以研究PD-L1表达和CD8+ TILs水平。采用多因素logistic回归分析临床特征与免疫标志物之间的关联。使用条件logistic回归模型计算比值比(OR)及其95%置信区间(CI),并采用Kaplan-Meier分析肿瘤复发。
肿瘤体积与PD-L1表达相关(P = 0.003,HR = 5.288,95%CI,1.786-15.651)。PTBE是CD8 + TIL水平的独立预测因子(P = 0.001,HR = 0.176,95%CI 0.065-0.477)。CD8 + TIL水平与肿瘤复发相关(P = 0.020,OR = 0.325,95%CI,0.125-0.840)。
To investigate the expression of programmed death ligand-1 (PD-L1) and the levels of CD8 + tumor-infiltrating lymphocytes (TILs) in meningioma as well as determine the association between their levels and the clinical outcomes.
We performed a retrospective case-control study on 93 patients with meningioma. The patients showed tumor recurrence and were matched with the control patients without recurrence in their age, gender, admission time, tumor sites, tumor volume, peritumoral brain edema (PTBE), Simpson grade resection, WHO grade, postoperative radiotherapy, and the follow-up duration. We reviewed the clinical data of patients and performed immunohistochemistry analysis to investigate the PD-L1 expression and the levels of CD8 + TILs. Multivariate logistic regression was performed to analyze the association between clinical features and immune markers. The conditional logistic regression models were used to calculate the odds ratios (ORs) with 95% confidence intervals (CIs), and Kaplan-Meier analysis was performed to analyze tumor recurrence.
Tumor volume was correlated with the PD-L1 expression (P = 0.003, HR = 5.288, 95%CI, 1.786-15.651). PTBE served as an independent predictor of CD8 + TIL levels (P = 0.001, HR = 0.176, 95%CI 0.065-0.477). The levels of CD8 + TILs were associated with tumor recurrence (P = 0.020, OR = 0.325, 95%CI, 0.125-0.840).
Tumor volume was associated with PD-L1 expression, and PTBE was an independent predictor of CD8 + TIL levels in meningioma. CD8 + TIL levels correlated with tumor recurrence in meningioma.
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