Evidence map›Paper›PMID 42185640›Full record

ArticleJournal of neuro-oncology2026

Liquid biopsy-based genomic risk score to predict neurologic death in non-small cell lung cancer patients.

Sarah E Glynn, Ralph D'Agostino, Claire M Lanier, Ariel R Choi, Michael Farris, Mohammed Abdulhaleem, Patrick Young, Yuezhu Wang, Margaret Smith, Jimmy Ruiz and 11 more

Abstract read
In one paragraph

Article in Journal of neuro-oncology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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0citing papers in PubMed
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1 · What the graph read from it

What it found

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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

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Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

21 authors.

Sarah E GlynnDepartment of Radiation Oncology, Wake Forest University School of Medicine, Winston Salem, NC, USA. sarah.glynn@advocatehealth.org.ORCID http://orcid.org/0000-0002-4382-3213
Ralph D'AgostinoDepartment of Biostatistics and Data Science, Wake Forest University School of Medicine, Winston Salem, NC, USA.
Claire M LanierDepartment of Radiation Oncology, Wake Forest University School of Medicine, Winston Salem, NC, USA.
Ariel R ChoiDepartment of Radiation Oncology, Wake Forest University School of Medicine, Winston Salem, NC, USA.
Michael FarrisDepartment of Radiation Oncology, Wake Forest University School of Medicine, Winston Salem, NC, USA.
Mohammed AbdulhaleemDepartment of Hospital Medicine, Wake Forest University School of Medicine, Winston Salem, NC, USA.
Patrick YoungDepartment of Radiation Oncology, Wake Forest University School of Medicine, Winston Salem, NC, USA.
Yuezhu WangDepartment of Molecular and Cellular Bioscience, Wake Forest University School of Medicine, Winston Salem, NC, USA.
Margaret SmithDepartment of Molecular and Cellular Bioscience, Wake Forest University School of Medicine, Winston Salem, NC, USA.
Jimmy RuizDepartment of Internal Medicine, Section of Hematology and Oncology, Wake Forest University School of Medicine, Winston Salem, NC, USA.
Thomas LycanDepartment of Internal Medicine, Section of Hematology and Oncology, Wake Forest University School of Medicine, Winston Salem, NC, USA.
William Jeffrey PettyDepartment of Internal Medicine, Section of Hematology and Oncology, Wake Forest University School of Medicine, Winston Salem, NC, USA.
Christina K CramerDepartment of Radiation Oncology, Wake Forest University School of Medicine, Winston Salem, NC, USA.
Stephen B TatterDepartment of Neurosurgery, Wake Forest University School of Medicine, Winston Salem, NC, USA.
Adrian W LaxtonDepartment of Neurosurgery, Wake Forest University School of Medicine, Winston Salem, NC, USA.
Jaclyn J WhiteDepartment of Neurosurgery, Wake Forest University School of Medicine, Winston Salem, NC, USA.
Jing SuDepartment of Biostatistics and Health Data Science, Indiana University School of Medicine, Indianapolis, IN, USA.
Christopher T WhitlowDepartment of Diagnostic Radiology, Wake Forest University School of Medicine, Winston Salem, NC, USA.
Fei XingDepartment of Cancer Biology, Wake Forest University School of Medicine, Winston Salem, NC, USA.
Michael D ChanDepartment of Radiation Oncology, Wake Forest University School of Medicine, Winston Salem, NC, USA.
Corbin A HelisDepartment of Radiation Oncology, Wake Forest University School of Medicine, Winston Salem, NC, USA.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

introductionBiomarkers that predict neurologic death may allow for personalization of therapy for high-risk brain metastases patients.

methodsPatients with NSCLC who underwent comprehensive genomic profiling were identified in an institutional database. Neurologic death was determined by medical record review. Proportional hazards regression models considering non-neurologic death as a competing risk were used to identify mutations statistically associated with the occurrence of neurologic death (p < 0.1) and to create a risk scoring system for neurologic death. A competing risk proportional hazards regression model with non-neurologic death as a competing risk was used to assess the association between the risk score and neurologic death, and to calculate hazard ratios predicting neurologic death between risk groups.

results307 patients were included in the primary analysis and 213 in a cohort of patients with brain metastases. Risk scores were constructed in both populations. Patients with higher risk scores had an increased risk of neurologic death when compared to those in the low-risk group, with respective HRs of 3.76 for the entire cohort and 2.87 for the brain metastasis cohort per unit increase in the risk score. When dividing the risk score into three groups, the cumulative incidence of neurologic death in high, moderate, and low risk groups was 49.0%, 20.3% and 0% for the entire cohort and 52.4%, 30.4%, and 0% in the brain metastasis cohort.

conclusionDevelopment of a genomic signature to predict neurologic death via non-invasive liquid biopsy appears feasible in NSCLC patients.

Indexed as

Biomarkers, TumorBrain NeoplasmsCarcinoma, Non-Small-Cell LungLung NeoplasmsAgedFemaleFollow-Up StudiesGenetic Risk ScoreGenomicsHumansLiquid BiopsyMaleMiddle AgedPrognosisRisk FactorsBiomarkers, TumorBrain deathBrain metastasesGenetic biomarkersNext generation sequencingNon-small cell lung cancerRadiotherapy

Identifiers

PMID42185640
PMCPMC13201357

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.