# Brain metastases from non-small cell lung cancer: molecular subtypes and emerging CNS-directed precision therapies

**Authors:** Mehek Sharma, Anvay Shah, Kimberly A. Rivera-Caraballo, Girindra Raval, Balveen Kaur, Gerald C. Wallace

PMC · DOI: 10.3389/fonc.2026.1717432 · 2026-01-22

## 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.

## Key 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 drug-delivery strategies including intraventricular or intranasal administration, focused ultrasound, nanocarriers, and efflux transporter modulation. Furthermore, we provide a comprehensive update on recent and ongoing preclinical and clinical studies, highlighting novel CNS-penetrant agents with demonstrated intracranial efficacy. Understanding these mechanisms and refining targeted approaches are critical to improving CNS disease control, survival outcomes, and quality of life for NSCLC patients with brain involvement.

## Linked entities

- **Genes:** EGFR (epidermal growth factor receptor) [NCBI Gene 1956], ALK (ALK receptor tyrosine kinase) [NCBI Gene 238], ROS1 (ROS proto-oncogene 1, receptor tyrosine kinase) [NCBI Gene 6098]
- **Proteins:** PDCD1 (programmed cell death 1), CD274 (CD274 molecule)
- **Diseases:** non-small-cell lung cancer (MONDO:0005233)

## Full-text entities

- **Genes:** ROS1 (ROS proto-oncogene 1, receptor tyrosine kinase) [NCBI Gene 6098] {aka MCF3, ROS, c-ros-1}, CD274 (CD274 molecule) [NCBI Gene 29126] {aka ADMIO5, B7-H, B7H1, PD-L1, PDCD1L1, PDCD1LG1}, EGFR (epidermal growth factor receptor) [NCBI Gene 1956] {aka ERBB, ERBB1, ERRP, HER1, NISBD2, NNCIS}, PDCD1 (programmed cell death 1) [NCBI Gene 5133] {aka ADMIO4, AIMTBS, CD279, PD-1, PD1, SLEB2}, ALK (ALK receptor tyrosine kinase) [NCBI Gene 238] {aka ALK1, CD246, NBLST3}
- **Diseases:** lung tumors (MESH:D008175), L (MESH:D007926), Brain metastases (MESH:D001932), NSCLC (MESH:D002289), metastasis (MESH:D009362)
- **Species:** Homo sapiens (human, species) [taxon 9606]

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Source: https://tomesphere.com/paper/PMC12872532