ArticleCommunications medicine2026
Cerebrospinal fluid cfDNA-based molecular assessment of resection extent and prognosis in glioma.
Article in Communications medicine, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.
What it found
Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.
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.
The trial behind it
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.
Who cites it
1 citing paper in PubMed.
- Cerebrospinal Fluid in Pediatric Neuro-Oncology: Molecular Diagnosis, Disease Monitoring, and Clinical Translation.International journal of molecular sciences · 2026Review
Corrections and comments
PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.
Authors and funding
10 authors.
Funding
No grant is acknowledged in the PubMed record.
Abstract
backgroundGliomas, the most common brain tumors, present significant challenges in treatment, particularly glioblastoma multiforme (GBM), due to their infiltrative nature and difficulty in achieving gross total resection (GTR). Accurate assessment of surgical resection extent is critical for patient prognosis and survival. This study investigates the utility of cerebrospinal fluid (CSF) cell-free DNA (cfDNA) as a quantitative biomarker for evaluating glioma resection extent and patient prognosis.
methodsNext-generation sequencing (NGS) was used to profile genomic alterations in tumor DNA and CSF cfDNA obtained before and after surgery. Concordance between mutations detected in tumor tissue and CSF cfDNA was assessed. Post-operative changes in mean mutant allele frequency (MAF) and tumor mutational burden (TMB) were evaluated, and their associations with overall survival (OS) were analyzed.
resultsA high concordance rate (83.50%) exists between CSF cfDNA and tumor tissue, particularly for key somatic mutations such as TERT, TP53, PTEN, and IDH1. Post-operative cfDNA analysis shows a significant reduction in mean MAF and TMB. Apart from non-GTR and multiple lesions, patients who exhibit a ≥ 90% reduction in mean MAF or in the MAF of driver mutations post-surgery demonstrate significantly improved OS.
conclusionsThese findings suggest that CSF cfDNA effectively represents the genetic profile of gliomas and serves as a sensitive measure for surgical resection efficacy and patient prognosis, highlighting its potential as a non-invasive biomarker for enhancing post-operative management in glioma patients.
Identifiers
What OpenQuestion holds
Registered trials
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.