Abstract 496P
Background
Given the diverse clinical presentation of brain metastases (BM) in non-small cell lung cancer (NSCLC), we aimed to investigate whether the neurological symptom burden correlates with the volume of the BM as well as the peritumoral edema in a real-world patient cohort.
Methods
Cranial magnetic resonance imaging at the time of BM diagnosis was retrospectively analyzed in patients with BM from NSCLC to determine the extent of BM volume and peritumoral edema volume. Volumes of BM and peritumoral edema were categorized into quartiles (class I-IV) for statistical analysis.
Results
312 patients with information on BM volume and peritumoral edema volume were included. The median BM volume was 2.78cm3 (range 0-82.4), while the median peritumoral edema volume was 25.6 cm3 (range 0-251). 248/312 (79.5%) patients presented with neurological symptoms at BM diagnosis. An increase of BM or peritumoral edema volume also showed an increased likelihood of neurological symptoms (BM volume: OR: 1.83; CI 1.43-2.43; p<0.001; edema volume: OR: 1.4; CI 1.25-1.58; p<0.001). In detail, a correlation between the presence of focal deficits with BM and edema volume (p<0.02), and a correlation between BM volume and signs of increased intracranial pressure (p=0.001) was found. In contrast, no statistically significant association was detected between epileptic seizures and BM or edema volume (p>0.05). Incorporating interaction terms into the analysis to investigate the correlation with sex, age, and localization of BM, we observed that the effect of BM or peritumoral edema volume remained consistent across these different levels (p>0.05). Both, peritumoral edema volume and BM volume, didn’t correlate with survival in univariate and multivariate models, while the presence of neurological symptoms at BM diagnosis (HR:1.46; CI 1.0-2.8, p=0.03) presented as independent prognostic factors.
Conclusions
In conclusion, larger volumes of BM or peritumoral edema correlated with an increased probability of neurological symptoms, but not with the occurrence of epileptic seizures. In contrast to neurological symptoms at BM diagnosis, BM volume and peritumoral edema volume were not associated with prognosis in our real-world patient cohort.
Clinical trial identification
Editorial acknowledgement
Legal entity responsible for the study
The authors.
Funding
Has not received any funding.
Disclosure
M. Preusser: Financial Interests, Personal, Advisory Board: Bayer, Bristol Myers Squibb, Novartis, Gerson Lehrman Group, CMC Contrast, GSK, Mundipharma, Roche, BMJ Journals, MedMedia, AstraZeneca, Daiichi Sankyo, Merck Sharp & Dome; Financial Interests, Personal, Speaker, Consultant, Advisor: Bayer, Bristol Myers Squibb, Novartis, Gerson Lehrman Group, CMC Contrast, GSK, Mundipharma, BMJ Journals, MedMedia, AstraZeneca, Daiichi Sankyo, Merck Sharp & Dome; Financial Interests, Personal, Invited Speaker: Bayer, Bristol Myers Squibb, Novartis, Gerson Lehrman Group, CMC Contrast, GSK, Mundipharma, Roche, BMJ Journals, MedMedia, AstraZeneca, Merck Sharp & Dome; Financial Interests, Institutional, Sponsor/Funding: Roche; Financial Interests, Personal, Sponsor/Funding: Daiichi Sankyo. A.S. Berghoff: Financial Interests, Institutional, Research Funding: Daiichi Sankyo; Financial Interests, Institutional, Research Grant: Rochee; Financial Interests, Speaker, Consultant, Advisor: Roche, Bristol Myers Squibb, Merck, Daiichi Sankyo; Financial Interests, Sponsor/Funding, Travel: Roche, Amgen, AbbVie, Daiichi Sankyo. All other authors have declared no conflicts of interest.
Resources from the same session
469P - Detection of circulating tumor DNA (ctDNA) in cerebrospinal fluid (CSF) in patients with glioblastoma treated in phase I clinical trial
Presenter: Marie Porte
Session: Poster session 16
470P - Mitochondrial ribosomal proteins (MRPs) in glioblastoma multiforme: Omics approach
Presenter: Jehad Yasin
Session: Poster session 16
471P - PTEN alteration as a predictor of second-line efficacy in patients with recurrent IDHwt-glioblastoma
Presenter: Eugenia Cella
Session: Poster session 16
472P - Comprehensive quinomics assessment of BPM31510IV treatment in advanced glioblastoma multiforme patients
Presenter: Seema Nagpal
Session: Poster session 16
473P - A novel machine learning (ML) model integrating clinical and molecular data to predict response to second-line treatment in recurrent IDHwt-glioblastoma (rGBM)
Presenter: Maurizio Polano
Session: Poster session 16
474P - Potassium inward rectifier channel subfamily J member 11 mRNA expression in glioma and its significance in predicting prognosis and chemotherapy sensitivity
Presenter: kaijia zhou
Session: Poster session 16
Resources:
Abstract
475P - Optimising genomic testing for patients with central nervous system (CNS) tumours using oxford nanopore technology
Presenter: Alona Sosinsky
Session: Poster session 16
476P - The role of androgen receptor expression and epigenetic regulation in adult-type diffuse gliomas
Presenter: VINCENZO DI NUNNO
Session: Poster session 16
477P - ENHO's protective role in lower grade glioma
Presenter: Osama Younis
Session: Poster session 16