Evidence map›Paper›PMID 42207360›Full record

ArticleJournal of neuro-oncology2026

Predicting late radiation-associated neurocognitive and endocrine toxicity in patients with brain tumors.

Kyle Tuohy, Aarav Badani, Ava Franklin, Brad Zacharia, Dawit Aregawi, Alireza Mansouri, Paul Brown, Michael Glantz

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.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

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.

2 · The registry

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.

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

8 authors.

Kyle TuohyDepartment of Neurosurgery, Penn State Hershey Medical Center, Hershey, PA, USA.
Aarav BadaniUniversity of California Berkeley, Berkeley, CA, USA.
Ava FranklinUniversity of Virginia, Charlottesville, VA, USA.
Brad ZachariaDepartment of Neurosurgery, Penn State Hershey Medical Center, Hershey, PA, USA.
Dawit AregawiDepartment of Neurosurgery, Penn State Hershey Medical Center, Hershey, PA, USA.
Alireza MansouriDepartment of Neurosurgery, Penn State Hershey Medical Center, Hershey, PA, USA.
Paul BrownDepartment of Radiation Oncology, Mayo Clinic, Rochester, MN, USA.
Michael GlantzDepartment of Neurosurgery, Penn State Hershey Medical Center, Hershey, PA, USA. mglantz@pennstatehealth.psu.edu.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

purposeNeurocognitive and endocrine dysfunction are potential complications of cranial irradiation. However, risk factors are poorly understood, impeding accurate prognostication and exploration of potential preventive interventions. The objective of this study was to evaluate the prognostic value of various vascular and genotypic risk factors for the development of radiation-related toxicities.

methodsThis single-institution retrospective cohort study included patients with metastatic and malignant primary brain tumors who received cranial irradiation as part of their initial tumor-directed therapy. Demographic and treatment characteristics were collected, as well as putative vascular and genotypic risk factors. Univariate, multivariate, and machine-learning analyses were performed using five pre-specified measures of radiation-related toxicity. The primary outcome was change in mini-mental status exam (MMSE).

resultsEighty patients (53% male, mean age 55.7, 53% primary and 44% metastatic brain tumors) were included. Elevated homocysteine and ApOE4 genotype were the strongest predictors of MMSE decline in the multivariate model (OR 3.96 [6.5-200, p < 0.001 and 2.85 [1.92-27.6], p = 0.004). Elevated homocysteine was associated white matter change on MRI and both physician and patient assessment. ApoE4 allele was associated with new endocrine deficiency, and physician assessment. An online nomogram provides risk predictions for each of the five late toxicity outcomes: ( https://afranklin22.shinyapps.io/PRMMSERadiationRiskFactors/ )

conclusionTwo pre-treatment laboratory values (elevated homocysteine and ApOE genotype) were strongly associated with post-radiation neurocognitive and endocrine dysfunction using a variety of domains. Our predictive algorithm can aid clinicians in stratifying baseline risk and should be validated in prospective trials and with additional metrics of ND.

Indexed as

Brain NeoplasmsCranial IrradiationEndocrine System DiseasesRadiation InjuriesAdultAgedFemaleFollow-Up StudiesHumansMachine LearningMaleMiddle AgedPrognosisRetrospective StudiesRisk FactorsBrain tumorsCognitive/endocrine dysfunctionCranial irradiationMachine learningNeurotoxicity

Identifiers

PMID42207360
PMCPMC13219158

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

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.