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抗 PD-1/PD-L1 检查点抑制剂治疗 NSCLC 患者中循环髓源抑制细胞 PD-L1 表达的预后意义。

Prognostic Significance of PD-L1 Expression on Circulating Myeloid-Derived Suppressor Cells in NSCLC Patients Treated with Anti-PD-1/PD-L1 Checkpoint Inhibitors.

机构信息

Functional Cytomics Lab, Germans Trias i Pujol Research Institute (IGTP), Campus Can Ruti, Crta. de Can Ruti, Camí de les Escoles, s/n, 08916 Badalona, Spain.

Department of Cellular Biology, Physiology and Immunology, Autonomous University of Barcelona (UAB), 08193 Cerdanyola del Vallès, Spain.

出版信息

Int J Mol Sci. 2024 Nov 15;25(22):12269. doi: 10.3390/ijms252212269.

Abstract

Even though anti-PD-1/PD-L1 immune checkpoint inhibitors (ICIs) in non-small cell lung cancer (NSCLC) have improved survival, a high percentage of patients still do not respond to ICIs. Myeloid-derived suppressor cells (MDSCs) are circulating cells that express PD-L1 and can infiltrate and proliferate in the tumor microenvironment, inducing immunosuppression. By evaluating changes in PD-L1 expression of live peripheral blood MDSCs, we are able to define a new PD-L1 index, useful in predicting ICI escape in NSCLC patients before initiating anti-PD-1/PD-L1 immunotherapy. In this study, a cohort of 37 NSCLC patients was prospectively analyzed, obtaining independent PD-L1 indexes. In patients with a PD-L1 index > 5.88, progressive disease occurred in 58.33% of patients [median progression-free survival (PFS) = 5.73 months; 95%CI = 2.67-20.53], showing significant differences when compared with patients with a PD-L1 index ≤ 5.88, in whom 7.69% progressed and median PFS was not reached (NR); -value = 0.0042. Overall survival (OS) was significantly worse in patients with a high vs. low PD-L1 index (41.67% vs. 76.92%; median OS = 18.03 months, 95%CI = 6.77-25.23 vs. NR, 95%CI = 1.87-NR; -value = 0.035). The PD-L1 index can be applied to stratify NSCLC patients according to their probability of response to ICIs at baseline. In addition to quantifying tumoral expression, this index could be used to compare nonresponse to treatment.

摘要

尽管抗 PD-1/PD-L1 免疫检查点抑制剂(ICI)在非小细胞肺癌(NSCLC)中的应用提高了生存率,但仍有很大比例的患者对 ICI 没有反应。髓源性抑制细胞(MDSCs)是表达 PD-L1 的循环细胞,可以浸润和增殖于肿瘤微环境中,诱导免疫抑制。通过评估活外周血 MDSC 中 PD-L1 的表达变化,我们能够定义一个新的 PD-L1 指数,该指数有助于在启动抗 PD-1/PD-L1 免疫治疗之前预测 NSCLC 患者对 ICI 的逃逸。在这项研究中,前瞻性分析了 37 例 NSCLC 患者队列,获得了独立的 PD-L1 指数。在 PD-L1 指数>5.88 的患者中,58.33%的患者出现疾病进展[中位无进展生存期(PFS)=5.73 个月;95%CI=2.67-20.53],与 PD-L1 指数≤5.88 的患者相比差异具有统计学意义,后者进展的患者比例为 7.69%,中位 PFS 未达到(NR);-值=0.0042。高 PD-L1 指数患者的总生存期(OS)明显差于低 PD-L1 指数患者(41.67%比 76.92%;中位 OS=18.03 个月,95%CI=6.77-25.23 比 NR,95%CI=1.87-NR;-值=0.035)。PD-L1 指数可用于根据患者对 ICI 的基线反应概率对 NSCLC 患者进行分层。除了定量评估肿瘤表达外,该指数还可用于比较治疗无反应。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/db07/11594642/f678ed975120/ijms-25-12269-g001.jpg

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