Evidence map›Paper›PMID 42867757›Full record

Observational studyJournal of neuro-oncology2026

Weekly hippocampal diffusion changes during partial-brain radiation therapy for high-grade glioma: associations with dose and early memory change.

Ory Haisraely, Bikash Panthi, Kyle Richard Noll, Eleni Konstantinopoulou, Andrew Elliott, Sara Thrower, Holly Langshaw, Wasif Talpur, Catherine Sullaway, Todd Swanson and 11 more

Abstract readObservational Study
In one paragraph

Observational study 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

21 authors.

Ory HaisraelyDepartment of Radiation Oncology, The University of Texas MD Anderson Cancer Center, 1515 Holcombe Blvd, Houston, TX, 77030, USA.ORCID http://orcid.org/0000-0001-6612-1866
Bikash PanthiDepartment of Radiation Oncology, The University of Texas MD Anderson Cancer Center, 1515 Holcombe Blvd, Houston, TX, 77030, USA.
Kyle Richard NollDepartment of Radiation Oncology, The University of Texas MD Anderson Cancer Center, 1515 Holcombe Blvd, Houston, TX, 77030, USA.ORCID http://orcid.org/0000-0002-7105-1900
Eleni KonstantinopoulouDepartment of Radiation Oncology, The University of Texas MD Anderson Cancer Center, 1515 Holcombe Blvd, Houston, TX, 77030, USA.ORCID http://orcid.org/0000-0003-4077-9648
Andrew ElliottDepartment of Radiation Oncology, The University of Texas MD Anderson Cancer Center, 1515 Holcombe Blvd, Houston, TX, 77030, USA.
Sara ThrowerDepartment of Radiation Physics, The University of Texas MD Anderson Cancer Center, Houston, TX, USA.ORCID http://orcid.org/0000-0001-9915-7443
Holly LangshawDepartment of Radiation Oncology, The University of Texas MD Anderson Cancer Center, 1515 Holcombe Blvd, Houston, TX, 77030, USA.
Wasif TalpurDepartment of Radiation Oncology, The University of Texas MD Anderson Cancer Center, 1515 Holcombe Blvd, Houston, TX, 77030, USA.
Catherine SullawayDepartment of Neuropsychology, The University of Texas MD Anderson Cancer Center, Houston, TX, USA.
Todd SwansonDepartment of Radiation Oncology, The University of Texas MD Anderson Cancer Center, 1515 Holcombe Blvd, Houston, TX, 77030, USA.
Chenyang WangDepartment of Radiation Oncology, The University of Texas MD Anderson Cancer Center, 1515 Holcombe Blvd, Houston, TX, 77030, USA.
Martin C TomDepartment of Radiation Oncology, The University of Texas MD Anderson Cancer Center, 1515 Holcombe Blvd, Houston, TX, 77030, USA.
Thomas BeckhamDepartment of Radiation Oncology, The University of Texas MD Anderson Cancer Center, 1515 Holcombe Blvd, Houston, TX, 77030, USA.
Wen JiangDepartment of Radiation Oncology, The University of Texas MD Anderson Cancer Center, 1515 Holcombe Blvd, Houston, TX, 77030, USA.
Debra Nana YeboaDepartment of Radiation Oncology, The University of Texas MD Anderson Cancer Center, 1515 Holcombe Blvd, Houston, TX, 77030, USA.
Mary Frances McAleerDepartment of Radiation Oncology, The University of Texas MD Anderson Cancer Center, 1515 Holcombe Blvd, Houston, TX, 77030, USA.
Amol GhiaDepartment of Radiation Oncology, The University of Texas MD Anderson Cancer Center, 1515 Holcombe Blvd, Houston, TX, 77030, USA.
Susan Lynne McGovernDepartment of Radiation Oncology, The University of Texas MD Anderson Cancer Center, 1515 Holcombe Blvd, Houston, TX, 77030, USA.
Jing LiDepartment of Radiation Oncology, The University of Texas MD Anderson Cancer Center, 1515 Holcombe Blvd, Houston, TX, 77030, USA.
Jeffrey Scott Wefel *Department of Radiation Oncology, The University of Texas MD Anderson Cancer Center, 1515 Holcombe Blvd, Houston, TX, 77030, USA.
Caroline Chung *Department of Radiation Oncology, The University of Texas MD Anderson Cancer Center, 1515 Holcombe Blvd, Houston, TX, 77030, USA. cchung3@mdanderson.org.ORCID http://orcid.org/0000-0002-9662-1519

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

purposeTo characterize the weekly trajectory of hippocampal diffusion during fractionated partial-brain radiation therapy (RT) for high-grade glioma and determine whether the magnitude of change is associated with planned hippocampal dose.

methodsForty-five adults enrolled in a prospective observational imaging study and treated with 60 Gy in 30 fractions with concurrent temozolomide underwent diffusion MRI before RT and weekly during treatment. Relative bilateral hippocampal apparent diffusion coefficient (ADC) change and fractional anisotropy (FA) were evaluated longitudinally. Linear mixed-effects models included treatment week and planned mean bilateral hippocampal dose as fixed main effects. A secondary laterally-specific analysis evaluated baseline-to-Week-6 ADC change separately in the hippocampi ipsilateral and contralateral to the tumor.

resultsHippocampal ADC increased progressively from a median relative change of 0.5% at Week 1 to 12% (IQR, 6%-18%) at Week 6. The ADC time coefficient was + 2.2% points per week (95% CI, 1.8-2.5; P < 0.001). After accounting for week, higher planned mean bilateral hippocampal dose was associated with greater ADC change (+ 0.81% points/Gy; 95% CI, 0.76-0.93; P < 0.001). In the secondary laterally-specific analysis, higher dose was associated with greater Week-6 ADC change in both the ipsilateral hippocampus (β = 0.83% points/Gy; 95% CI, 0.52-1.26; P = 0.013) and the contralateral hippocampus (β = 0.36% points/Gy; 95% CI, 0.05-0.712; P = 0.046). FA remained stable through Week 3 and declined during Weeks 4-6.

conclusionWeekly diffusion MRI demonstrates a progressive, dose-associated hippocampal response during fractionated RT. The laterality-specific findings further support an association between local radiation exposure and ADC change and support hippocampal ADC as a candidate treatment-phase imaging phenotype for prospective validation.

Indexed as

Brain NeoplasmsCranial IrradiationGliomaHippocampusMemory DisordersAdultAgedDiffusion Magnetic Resonance ImagingFemaleFollow-Up StudiesHumansMaleMiddle AgedNeoplasm GradingProspective StudiesTemozolomideTemozolomideApparent diffusion coefficientDiffusion MRIHigh-grade gliomaHippocampusRadiation therapy

Identifiers

PMID42867757
PMCPMC13661711

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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.