Department of Medical Oncology, Catalan Institute of Oncology, Hospital Duran i Reynals, Avinguda de la Gran Via de l'Hospitalet, 199-203, L'Hospitalet de Llobregat, Barcelona, Spain; Clinical Research in Solid Tumors (CReST) Group, Molecular Mechanisms and Experimental Therapeutics in Cancer (Oncobell). IDIBELL, Avinguda de la Gran Via de l'Hospitalet, 199-203, L'Hospitalet de Llobregat, Barcelona, Spain.
Neuro-Oncology Unit, Bellvitge University Hospital-ICO (IDIBELL), Avinguda de la Gran Via de l'Hospitalet, 199-203, L'Hospitalet de Llobregat, Barcelona, Spain.
Cancer Treat Rev. 2020 Sep;89:102067. doi: 10.1016/j.ctrv.2020.102067. Epub 2020 Jul 7.
Brain metastases are frequent complications in patients with non-small-cell lung cancer (NSCLC) associated with significant morbidity and poor prognosis. Our goal is to give a global overlook on clinical efficacy from immune checkpoint inhibitors in this setting and to review the role of biomarkers and molecular interactions in brain metastases from patients with NSCLC.
We reviewed clinical trials reporting clinical outcomes of patients with NSCLC with brain metastases as well as publications assessing the tumor microenvironment and the complex molecular interactions of tumor cells with immune and resident cells in brain metastases from NSCLC biopsies or preclinical models.
Although limited data are available on immunotherapy in patients with brain metastases, immune checkpoint inhibitors alone or in combination with chemotherapy have shown promising intracranial efficacy and safety results. The underlying mechanism of action of immune checkpoint inhibitors in the brain niche and their influence on tumor microenvironment are still not known. Lower PD-L1 expression and less T CD8 infiltration were found in brain metastases compared with matched NSCLC primary tumors, suggesting an immunosuppressive microenvironment in the brain. Reactive astrocytes and tumor associated macrophages are paramount in NSCLC brain metastases and play a role in promoting tumor progression and immune evasion.
Discordances in the immune profile between primary tumours and brain metastases underscore differences in the tumour microenvironment and immune system interactions within the lung and brain niche. The characterization of immune phenotype of brain metastases and dissecting the interplay among immune cells and resident stromal cells along with cancer cells is crucial to unravel effective immunotherapeutic approaches in patients with NSCLC and brain metastases.
脑转移是与显著发病率和预后不良相关的非小细胞肺癌(NSCLC)患者的常见并发症。我们的目标是全面概述免疫检查点抑制剂在这一背景下的临床疗效,并回顾 NSCLC 脑转移患者的生物标志物和分子相互作用的作用。
我们回顾了报告 NSCLC 伴脑转移患者临床结局的临床试验报告,以及评估 NSCLC 脑转移活检或临床前模型中肿瘤微环境以及肿瘤细胞与免疫和固有细胞复杂分子相互作用的出版物。
尽管脑转移患者的免疫治疗数据有限,但单独使用免疫检查点抑制剂或联合化疗已显示出有希望的颅内疗效和安全性结果。免疫检查点抑制剂在脑龛中的作用机制及其对肿瘤微环境的影响尚不清楚。与匹配的 NSCLC 原发性肿瘤相比,脑转移中 PD-L1 表达较低且 T CD8 浸润较少,表明脑内存在免疫抑制微环境。反应性星形胶质细胞和肿瘤相关巨噬细胞在 NSCLC 脑转移中至关重要,它们在促进肿瘤进展和免疫逃逸中发挥作用。
原发肿瘤和脑转移之间免疫谱的差异突显了肺部和脑龛内肿瘤微环境和免疫系统相互作用的差异。脑转移的免疫表型特征的表征以及解析免疫细胞与固有基质细胞以及癌细胞之间的相互作用对于揭示 NSCLC 和脑转移患者的有效免疫治疗方法至关重要。