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非小细胞肺癌脑转移患者的免疫检查点抑制:新出现的机制和个性化临床策略

Immune Checkpoint Inhibition in Patients with Brain Metastases from Non-Small-Cell Lung Cancer: Emerging Mechanisms and Personalized Clinical Strategies.

作者信息

Nasser Nicola J, Sindhu Kunal K, Nasser Loor, Shafaee Zahra, Li Joshua, Resende Salgado Lucas, Li Baoqing

机构信息

The Mount Sinai Hospital, Icahn School of Medicine at Mount Sinai, New York, NY 10029, USA.

Riverdale Kingsbridge Academy, Bronx, NY 10463, USA.

出版信息

Int J Mol Sci. 2025 Sep 4;26(17):8624. doi: 10.3390/ijms26178624.

DOI:10.3390/ijms26178624
PMID:40943541
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC12429631/
Abstract

Brain metastases are a significant complication of non-small-cell lung cancer (NSCLC), contributing to high morbidity and mortality rates. The introduction of immune checkpoint inhibitors (ICIs) has opened new therapeutic avenues for patients with NSCLC, including those with brain metastases. However, the distinct microenvironment of the brain presents unique challenges to the effectiveness of these treatments. This review examines the mechanisms by which ICIs impact brain metastases from NSCLC, with particular focus on immune cell trafficking across the blood-brain barrier (BBB), tumor microenvironment modulation, and transcriptomic evolution of brain-tropic tumor clones. Unlike prior reviews, we integrate emerging data from single-cell and spatial transcriptomic studies, BBB disruption mechanisms, and the tumor-supportive role of brain-resident glia. We also critically evaluate key clinical trials and real-world evidence, highlighting differences in ICI efficacy across patient subgroups and therapeutic contexts. Additionally, we address the evolving role of surgical resection, stereotactic radiosurgery, and cerebrospinal-fluid-based biomarkers in optimizing ICI-based treatment strategies. This synthesis provides a comprehensive, mechanistic, and clinically relevant framework for improving outcomes in patients with NSCLC brain metastases treated with immunotherapy.

摘要

脑转移是非小细胞肺癌(NSCLC)的一种重要并发症,会导致高发病率和死亡率。免疫检查点抑制剂(ICI)的引入为NSCLC患者,包括那些有脑转移的患者,开辟了新的治疗途径。然而,大脑独特的微环境给这些治疗的有效性带来了独特的挑战。本综述探讨了ICI影响NSCLC脑转移的机制,特别关注免疫细胞穿越血脑屏障(BBB)的过程、肿瘤微环境的调节以及脑靶向肿瘤克隆的转录组进化。与以往的综述不同,我们整合了来自单细胞和空间转录组研究的新数据、BBB破坏机制以及脑内常驻神经胶质细胞的肿瘤支持作用。我们还严格评估了关键临床试验和真实世界证据,突出了ICI在不同患者亚组和治疗背景下疗效的差异。此外,我们讨论了手术切除、立体定向放射外科以及基于脑脊液的生物标志物在优化基于ICI的治疗策略中不断演变的作用。这一综合内容为改善接受免疫治疗的NSCLC脑转移患者的治疗结果提供了一个全面、基于机制且与临床相关的框架。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1b37/12429631/31f2a05475a6/ijms-26-08624-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1b37/12429631/4fa5de64436b/ijms-26-08624-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1b37/12429631/725e20c299a0/ijms-26-08624-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1b37/12429631/31f2a05475a6/ijms-26-08624-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1b37/12429631/4fa5de64436b/ijms-26-08624-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1b37/12429631/725e20c299a0/ijms-26-08624-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1b37/12429631/31f2a05475a6/ijms-26-08624-g003.jpg

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本文引用的文献

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