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免疫检查点抑制剂作为无驱动突变 IV 期 NSCLC 脑转移患者的一线治疗药物。

Immune checkpoint inhibitors as first-line treatment for brain metastases in stage IV NSCLC patients without driver mutations.

机构信息

Medical Oncology Department - La Fe Hospital, Valencia, Spain; Biomarker and Precision Medicine Unit - Health Research Institute La Fe Hospital, Valencia, Spain.

Biomarker and Precision Medicine Unit - Health Research Institute La Fe Hospital, Valencia, Spain.

出版信息

Cancer Lett. 2024 Dec 1;606:217317. doi: 10.1016/j.canlet.2024.217317. Epub 2024 Nov 1.

Abstract

Immune checkpoint inhibitors (ICI) therapy with or without chemotherapy has been established as the first-line treatment for patients with non-oncogene addicted advanced Non-Small Cell Lung Cancer (NSCLC). Yet some clinical settings, such as the treatment sequence in patients with brain metastases, have barely been evidenced. Although ICIs cannot directly cross the blood-brain barrier (BBB), evidence suggests that BBB damage could allow ICIs into the central nervous system, or that they can have an indirect effect on the tumor immune microenvironment (TIME) and cause an anti-tumor response. Pivotal phase III trials have included a highly selected population but offer few data on these patients. Here we first review how ICIs can indirectly shape the brain metastases microenvironment through different mechanisms, and some possible causes of ICIs resistance. We also analyze the evidence reported in pivotal phase III trials and phase II trials focused on NSCLC brain metastases for first-line treatment, and the evidence for upfront or delayed local brain therapy. Finally, we discuss the best evidence-based approach to treat NSCLC patients with brain metastases and propose future research.

摘要

免疫检查点抑制剂(ICI)联合或不联合化疗已被确立为非成瘾性晚期非小细胞肺癌(NSCLC)患者的一线治疗方法。然而,一些临床情况,如脑转移患者的治疗顺序,几乎没有证据支持。尽管 ICI 不能直接穿过血脑屏障(BBB),但有证据表明,BBB 损伤可能允许 ICI 进入中枢神经系统,或者它们可以对肿瘤免疫微环境(TIME)产生间接影响并引起抗肿瘤反应。关键性的 III 期试验纳入了高度选择的人群,但这些患者的数据很少。在这里,我们首先回顾 ICI 如何通过不同的机制间接塑造脑转移微环境,以及 ICI 耐药的一些可能原因。我们还分析了关键性 III 期试验和针对 NSCLC 脑转移的 II 期试验中报告的一线治疗证据,以及局部脑治疗的前期或延迟证据。最后,我们讨论了治疗 NSCLC 脑转移患者的最佳循证方法,并提出了未来的研究方向。

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