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Updated: Jan 20, 2026

A Brain Tumor/Organotypic Slice Co-culture System for Studying Tumor Microenvironment and Targeted Drug Therapies
Published on: November 7, 2015
[Basis of Tumor Microenvironment Relevant to Immunotherapies for Brain Metastases of NSCLC]
Qing Lan1, Chunxia Ji1, Yu Yao1
1Immunology Laboratory, Neurosurgical Institute of Fudan University; Department of Neurosurgery, Huashan Hospital, Fudan University, Shanghai 200040, China.
Abstract:
Brain is the most frequent site for distant metastases of non-small cell lung cancer (NSCLC). Brain metastasis (BM) is also the leading cause of disabilities and death in advanced NSCLC. In recent years, the application and effectiveness of small-molecule tyrosine kinase inhibitors has formed the basis for the treatment of NSCLC brain metastases with driver gene mutations. With the development of programmed cell death protein 1 (PD-1)/programmed cell death protein ligand 1 (PD-L1) inhibitors and relevant combination therapies, immunotherapy has become an important choice for non-classic oncogene addicted NSCLC BM patients. Also, the roles of relevant biomarkers are increasingly standing out. By reason of the particular immunopathological features of NSCLC brain metastases and its microenvironment, the aim of this review is to summarize relevant research progresses and provide more references for combination strategies of different therapeutic methods as well as the development of novel immunotherapies. .
Insights
Treatments for non-small cell lung cancer (NSCLC) brain metastases (BM) are evolving. Tyrosine kinase inhibitors and immunotherapy, including programmed cell death protein 1 (PD-1)/programmed cell death protein ligand 1 (PD-L1) inhibitors, offer new options for NSCLC BM patients.
Area of Science:
- Oncology
- Neurology
- Immunology
Background:
- Brain metastases (BM) are a frequent and severe complication of non-small cell lung cancer (NSCLC).
- BM significantly contributes to disability and mortality in advanced NSCLC patients.
- The unique tumor microenvironment of NSCLC BM influences treatment efficacy.
Purpose of the Study:
- To review recent advancements in treating NSCLC BM.
- To explore the role of targeted therapies and immunotherapies.
- To provide insights into combination strategies and novel immunotherapeutic approaches for NSCLC BM.
Main Methods:
- Literature review of recent research on NSCLC BM treatments.
- Analysis of targeted therapies, including tyrosine kinase inhibitors.
- Evaluation of immunotherapy, focusing on PD-1/PD-L1 inhibitors and combination therapies.
Main Results:
- Small-molecule tyrosine kinase inhibitors are effective for NSCLC BM with driver gene mutations.
- Immunotherapy, particularly PD-1/PD-L1 inhibitors, is a key option for patients without classic oncogene addiction.
- Biomarker roles in NSCLC BM treatment are becoming increasingly significant.
Conclusions:
- Combination strategies integrating targeted therapy and immunotherapy show promise for NSCLC BM.
- Understanding the immunopathology of the brain metastasis microenvironment is crucial for developing novel treatments.
- Further research is needed to optimize therapeutic approaches and develop new immunotherapies for NSCLC BM.
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