Brain metastases from non-small cell lung cancer: molecular subtypes and emerging CNS-directed precision therapies
Mehek Sharma, Anvay Shah, Kimberly A. Rivera-Caraballo, Girindra Raval, Balveen Kaur, Gerald C. Wallace

TL;DR
This review discusses how non-small cell lung cancer spreads to the brain and explores new treatments to improve outcomes for affected patients.
Contribution
The paper provides a comprehensive overview of molecular drivers and emerging CNS-targeted therapies for NSCLC brain metastases.
Findings
NSCLC brain metastases exhibit unique molecular adaptations compared to primary tumors.
New drug delivery methods like nanocarriers and focused ultrasound are being explored to overcome the blood-brain barrier.
Recent clinical studies highlight CNS-penetrant agents showing intracranial efficacy.
Abstract
Non-small-cell lung cancer (NSCLC) is a leading cause of morbidity and mortality globally, due in large part to the development of NSCLC-associated brain metastases (L-BM). Upon initial presentation, 11-26% of patients with NSCLC will have L-BM, while half of patients with NSCLC will develop L-BM over the course of their disease. The emergence of PD-1/PD-L1 immunotherapy and targeted therapies for EGFR, ALK, and ROS1 mutations has transformed the treatment landscape and improved outcomes for select patient populations. CNS progression remains a major challenge due to therapy resistance, the blood–brain barrier (BBB), and the unique molecular and transcriptomic adaptations exhibited by NSCLC brain metastases which differs markedly from primary lung tumors. In this review, we examine the molecular drivers of CNS metastasis, oncogenic signaling-targeted therapies, and next-generation CNS…
Genes, proteins, chemicals, diseases, species, mutations and cell lines named across the full text — each resolved to its canonical identifier and authoritative record.
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Taxonomy
TopicsBrain Metastases and Treatment · Lung Cancer Research Studies · Lung Cancer Treatments and Mutations
