Department of Pathology and Laboratory Medicine, Dartmouth-Hitchcock Medical Center, Geisel School of Medicine at Dartmouth, Lebanon, NH 03756, USA.
Division of Hematology/Oncology, Department of Medicine, University of California at San Francisco, San Francisco, CA 94143, USA.
Int J Mol Sci. 2024 Feb 7;25(4):2044. doi: 10.3390/ijms25042044.
Brain metastases represent a significant clinical challenge in the treatment of non-small-cell lung cancer (NSCLC), often leading to a severe decline in patient prognosis and survival. Recent advances in imaging and systemic treatments have increased the detection rates of brain metastases, yet clinical outcomes remain dismal due to the complexity of the metastatic tumor microenvironment (TME) and the lack of specific biomarkers for early detection and targeted therapy. The intricate interplay between NSCLC tumor cells and the surrounding TME in brain metastases is pivotal, influencing tumor progression, immune evasion, and response to therapy. This underscores the necessity for a deeper understanding of the molecular underpinnings of brain metastases, tumor microenvironment, and the identification of actionable biomarkers that can inform multimodal treatment approaches. The goal of this review is to synthesize current insights into the TME and elucidate molecular mechanisms in NSCLC brain metastases. Furthermore, we will explore the promising horizon of emerging biomarkers, both tissue- and liquid-based, that hold the potential to radically transform the treatment strategies and the enhancement of patient outcomes.
脑转移是治疗非小细胞肺癌(NSCLC)的一个重大临床挑战,常导致患者预后和生存严重恶化。成像和全身治疗的最新进展提高了脑转移的检出率,但由于转移瘤微环境(TME)的复杂性以及缺乏用于早期检测和靶向治疗的特异性生物标志物,临床结果仍不理想。NSCLC 肿瘤细胞与脑转移中周围 TME 的复杂相互作用至关重要,影响肿瘤进展、免疫逃逸和对治疗的反应。这凸显了深入了解脑转移的分子基础、肿瘤微环境以及鉴定可告知多模式治疗方法的可行生物标志物的必要性。本文综述的目的是综合目前对 TME 的认识,并阐明 NSCLC 脑转移中的分子机制。此外,我们还将探讨新兴生物标志物的广阔前景,包括组织和液体生物标志物,它们有可能彻底改变治疗策略并提高患者的预后。