一种用于克服非小细胞肺癌治疗中抗原异质性的多靶向 CAR-T 细胞平台
A Multi-Targeting Chimeric Antigen Receptor-T Cell Platform to Overcome Antigen Heterogeneity in the Treatment of Non-Small Cell Lung Cancer.
这些发现支持采用多靶点CAR-T 策略来应对NSCLC及可能其他实体瘤中的抗原异质性。
CELL INTELLIGENCE · 肿瘤细胞治疗研究
肿瘤细胞治疗研究
英文原题:Smoking History Predicts High Presence of TILs and Efficacy of PD-1 Blockade in PD-L1 Expression-negative Non-small Cell Lung Cancer Patients.
Smoking History Predicts High Presence of TILs and Efficacy of PD-1 Blockade in PD-L1 Expression-negative Non-small Cell Lung Cancer Patients.
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肿瘤细胞上程序性死亡配体1(PD-L1)的表达是程序性细胞死亡1(PD-1)阻断治疗的预测性生物标志物。本研究旨在阐明nivolumab在PD-L1表达阴性的非小细胞肺癌(NSCLC)患者中疗效的预测因素。
我们回顾性分析了2016年1月至2019年4月间晚期NSCLC患者的病历,并探究了nivolumab的预测标志物,包括CD8+TIL(肿瘤浸润淋巴细胞)(TILs)的状态。
共纳入70例NSCLC患者。重度吸烟史患者(吸烟指数:SI≥600)的总体缓解率(ORR)和无进展生存期(PFS)优于无重度吸烟史患者(SI<600)[ORR:20.6% vs. 2.8%,(p=0.02);PFS:2.4个月 vs. 1.8个月,(p=0.04)]。高密度CD8 + TIL与重度吸烟史显著相关(p=0.04)。结论:重度吸烟史(SI≥600)与大量CD8 + TIL相关,可能是nivolumab在PD-L1表达阴性肿瘤NSCLC患者中疗效的预测因素。
We retrospectively reviewed the records of advanced NSCLC patients between January 2016 and April 2019, and investigated the predictive marker of nivolumab including the status of CD8 + tumor infiltrating lymphocytes (TILs).
A total of 70 NSCLC patients were included. Overall response rate (ORR) and progression-free survival (PFS) were better in patients with a heavy smoking history (smoking index: SI≥600) than in those without (SI<600) [ORR: 20.6% vs. 2.8%, (p=0.02), and PFS: 2.4 months vs. 1.8 months, (p=0.04)]. A high density of CD8 + TILs was significantly associated with a heavy smoking history (p=0.04). Conlusion: Heavy smoking history (SI≥600), which was correlated with a large number of CD8 + TILs, could be a predictor of the efficacy of nivolumab in NSCLC patients with PD-L1 expression-negative tumors.
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