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Management of Brain Metastases in Non-Small-Cell Lung Cancer
Vinicius Ernani1, Thomas E Stinchcombe2
1Fred and Pamela Buffett Cancer Center/University of Nebraska Medical Center, Omaha, NE.
Journal of Oncology Practice
|November 13, 2019
Summary
Treatments for non-small-cell lung cancer (NSCLC) with brain metastases (BMs) are evolving. Targeted therapies and tyrosine kinase inhibitors show efficacy against CNS metastases, potentially delaying local treatments.
Area of Science:
- Oncology
- Neurology
- Pharmacology
Background:
- Lung cancer is a leading cause of cancer death, with brain metastases (BMs) occurring in approximately 20% of patients.
- Traditional treatments for NSCLC with BMs include surgery, stereotactic radiosurgery, and whole-brain radiation therapy.
- The advent of targeted therapies has complicated and advanced treatment strategies for BMs.
Purpose of the Study:
- To review current data on the management of non-small-cell lung cancer (NSCLC) with brain metastases (BMs).
- To discuss the evolving role of tyrosine kinase inhibitors (TKIs) and immunotherapy in treating CNS metastases from NSCLC.
- To outline an approach for managing NSCLC patients with BMs.
Main Methods:
- Review of current literature and clinical data.
- Analysis of the efficacy of tyrosine kinase inhibitors (TKIs) against central nervous system (CNS) metastases.
- Evaluation of the emerging role of immune checkpoint inhibitors in NSCLC with BMs.
Main Results:
- Many TKIs demonstrate significant and lasting efficacy against CNS metastases, often deferring the need for local therapy.
- TKIs can reduce the risk of CNS progression in patients with NSCLC.
- The role of immunotherapy in NSCLC with BMs is under active investigation.
Conclusions:
- Tyrosine kinase inhibitors represent a significant advancement in treating non-small-cell lung cancer brain metastases.
- Further research is needed to define the optimal role of immunotherapy in this patient population.
- A multidisciplinary approach is essential for managing NSCLC patients with BMs.

