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Abstract Details

Clinical Efficacy of Immune Checkpoint Inhibitors in Glioblastoma and Brain Metastases
Neuro-oncology
P3 - Poster Session 3 (5:00 PM-6:00 PM)
6-001

To investigate existing clinical trial results on the use of ICIs against primary cancers and brain metastases from melanoma, non-small cell lung cancer (NSCLC), and breast cancer.

 

Brain tumors, including glioblastoma (GBM) and metastatic lesions, are highly aggressive, treatment-resistant, and have a poor prognosis. Immune checkpoint inhibitors (ICIs) are a type of immunotherapy that aids the patient’s immune system in killing cancer cells, often administered alongside other therapies in highly aggressive cancers.  

A systematic review was conducted based on clinical trials evaluating ICIs for the treatment of GBM and brain metastases. An initial search of three electronic databases (Embase, Ovid MEDLINE, and Web of Science) identified 417 peer-reviewed articles. After applying the inclusion criteria and completing screening of Tier I (160 articles) and Tier II (12 articles), 7 studies were retained for final analysis. Eligible studies were English-language clinical trials published between 2015 and 2025 that enrolled adult participants (≥18 years), included a control arm, and reported results.

 

The analyzed studies evaluated overall survival (OS) and progression-free survival (PFS) in patients with newly diagnosed and recurrent GBM, including both MGMT-methylated and MGMT-unmethylated tumors. Treatment strategies included nivolumab as monotherapy or in combination with radiotherapy, temozolomide, or ipilimumab; ipilimumab with temozolomide. Across these studies, neither OS nor PFS improved compared with the respective control arms in GBM. The only trial to report a significant PFS extension used pembrolizumab in combination with pemetrexed and platinum chemotherapy in patients with NSCLC.

 

ICIs offer a promising strategy for brain metastases, specifically NSCLC, enhancing immune activation and integrating well with multimodal treatments. However, GBM’s immunosuppressive microenvironment poses significant barriers, limiting ICI efficacy in larger trials. There were no significant changes in OS or PFS with ICI treatment for GBM. Further studies are warranted to define the role of ICIs in the management of brain metastases.

Authors/Disclosures
Maria Fioletova
PRESENTER
Mrs. Fioletova has nothing to disclose.
Alena Khalil Ms. Khalil has nothing to disclose.
Emma Baker Ms. Baker has nothing to disclose.
Vito G. Evola, Medical Student Mr. Evola has nothing to disclose.
Joshua Costin, PhD Prof. Costin has nothing to disclose.
Samiksha Prasad, PhD Dr. Prasad has nothing to disclose.
Steven Vanni, DO Dr. Vanni has received personal compensation in the range of $500-$4,999 for serving as a Consultant for Xtant. Dr. Vanni has received personal compensation in the range of $100,000-$499,999 for serving as an Expert Witness for Attorneys . Dr. Vanni has received intellectual property interests from a discovery or technology relating to health care.
Regina M. Graham, PhD The institution of Dr. Graham has received research support from HCA Florida University Hospital.