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
576P - Safety and efficacy of IBI354 (anti-HER2 ADC) in patients (pts) with advanced gastrointestinal (GI) cancers: Results from a phase I study
Presenter: Jifang Gong
Session: Poster session 16
577P - Results of the phase Ib study of NC410 combined with pembrolizumab in MSS/MSI-L colorectal cancer patients
Presenter: Eric Christenson
Session: Poster session 16
579P - Intratumoral fusobacterium as prognostic factor in early stage colorectal cancer: Results of the FUSOMAP study
Presenter: Paolo Nuciforo
Session: Poster session 16
581P - mRNA profiling as a biomarker of prognosis and response to first-line treatment in metastatic colorectal cancer: Discovery and validation of a gene expression signature in three randomized trials
Presenter: Marco Germani
Session: Poster session 16
582P - Prognostic role of macrophage infiltration and monocyte-to-lymphocyte ratio in stage III colon cancer: The MIRROR study
Presenter: debora basile
Session: Poster session 16
583P - COMPReS study: Multiomic profiling reveals organ-specific differences in metastases and identifies novel predictive biomarkers in relapsed localized colon cancer
Presenter: Blanca García-Mico
Session: Poster session 16
584P - Genomic and transcriptomic characterization of peritoneal, lung and liver metastases of colorectal carcinoma reveals site-specific differences
Presenter: Nerma Crnovrsanin
Session: Poster session 16
585P - Prospective validation of the metastatic colon cancer score (mCCS) in patients with RAS wild-type metastatic colorectal cancer treated with first-line panitumumab plus FOLFIRI/FOLFOX: Final results of the non-interventional study VALIDATE
Presenter: Norbert Marschner
Session: Poster session 16