Evidence map›Paper›PMID 40443040›Full record

ArticleNeuro-oncology2025

Impact of corticosteroid administration on contrast-enhancing volume and diffusion MRI in treatment naïve glioblastoma.

Francesco Sanvito, Asher Kim, Catalina Raymond, Ashley Teraishi, Richard G Everson, Phioanh L Nghiemphu, Albert Lai, Robert A Chong, David A Nathanson, Noriko Salamon and 3 more

Abstract read
In one paragraph

Article in Neuro-oncology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed, 1 pooled it
–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

7 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. Pooled it
  2. Article
  3. Article
  4. Article
  5. Review
  6. Article
  7. Article
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

13 authors.

Francesco SanvitoDepartment of Radiological Sciences, David Geffen School of Medicine, University of California at Los Angeles, Los Angeles, California.ORCID 0000-0003-3379-9958
Asher KimDepartment of Bioengineering, Henry Samueli School of Engineering and Applied Science, University of California at Los Angeles, Los Angeles, California.
Catalina RaymondDepartment of Radiological Sciences, David Geffen School of Medicine, University of California at Los Angeles, Los Angeles, California.ORCID 0000-0003-2757-439X
Ashley TeraishiDepartment of Radiological Sciences, David Geffen School of Medicine, University of California at Los Angeles, Los Angeles, California.
Richard G EversonDepartment of Neurosurgery, David Geffen School of Medicine, University of California at Los Angeles, Los Angeles, California.
Phioanh L NghiemphuDepartment of Neurology, David Geffen School of Medicine, University of California at Los Angeles, Los Angeles, California.ORCID 0000-0003-4064-6079
Albert LaiDepartment of Neurology, David Geffen School of Medicine, University of California at Los Angeles, Los Angeles, California.ORCID 0000-0002-7265-2986
Robert A ChongDepartment of Neurology, David Geffen School of Medicine, University of California at Los Angeles, Los Angeles, California.
David A NathansonDepartment of Pharmacology, David Geffen School of Medicine, University of California at Los Angeles, Los Angeles, California.
Noriko SalamonDepartment of Radiological Sciences, David Geffen School of Medicine, University of California at Los Angeles, Los Angeles, California.ORCID 0000-0002-3520-9467
Timothy F CloughesyUCLA Neuro-Oncology Program, David Geffen School of Medicine, University of California at Los Angeles, Los Angeles, California.
Jingwen YaoDepartment of Bioengineering, Henry Samueli School of Engineering and Applied Science, University of California at Los Angeles, Los Angeles, California.
Benjamin M EllingsonDepartment of Psychiatry, David Geffen School of Medicine, University of California at Los Angeles, Los Angeles, California.ORCID 0000-0002-2764-6640

Funding

UCLA SPORE in Brain CancerP50CA211015 · NCI · UNIVERSITY OF CALIFORNIA LOS ANGELES · PI Yvonne Yu-Hsuan Chen · 2017 to 2026
$25.2M
Role of decorin and diffusion MRI in anti-VEGF efficacy for recurrent glioblastomaR01CA270027 · NCI · UNIVERSITY OF CALIFORNIA LOS ANGELES · PI TIMOTHY CLOUGHESY, Benjamin M. Ellingson · 2022 to 2026
$3.0M
Quantitative molecular MR-PET imaging of glycolysis in glioblastomaR01CA279984 · NCI · UNIVERSITY OF CALIFORNIA LOS ANGELES · PI Benjamin M. Ellingson, David A. Nathanson · 2023 to 2026
$2.4M
NCI NIH HHS P50 CA211015NCI NIH HHS R01 CA270027NCI NIH HHS R01 CA279984NIH/NCI R01CA270027
6 · The paper itself

Abstract

backgroundCorticosteroids impact the radiographic interpretation of glioblastoma, including artificial reduction in the contrast-enhancing tumor volume and intensity (i.e., a "pseudoresponse") and in the apparent diffusion coefficient (ADC). This study aimed to estimate the influence of corticosteroids on these measurements in treatment naïve glioblastoma before surgery.

methodsFifty-seven pairs of MRI scans from 54 patients with presurgical treatment-naïve glioblastoma were retrospectively grouped as increased (n = 29, all corticosteroid-free at baseline), stable (n = 25), or decreased (n = 3) corticosteroid dose between scans (median interval: 15 days). Tumor size and ADC changes between timepoints were compared between lesions with increased and stable corticosteroids. Volumetric changes ascribable to increased corticosteroid dose was modeled, adjusting for the time between scans.

resultsIncreased corticosteroid dose showed an observed volumetric shrinkage of the contrast-enhancing tumor (median: -23.7%) and reduction in estimated growth rates (median: -2.48% per day), significantly different (P < .0001) from the control group receiving a stable dose (median: +36.0% volume; +2.08% growth rate). When adjusting for the time interval between scans, the estimated corticosteroid-induced volumetric shrinkage was 44.0% (P < .0001, 95% CI, 25.7%-62.2%). Increased corticosteroid dose also decreased ADC in the contrast-enhancing tumor (median reduction: 180, IQR = 39 - 281 × 10-6 mm2/s, P = .0005).

conclusionCorticosteroid administration can induce a significant "pseudoresponse" in glioblastoma, with an observed reduction in contrast-enhancing tumor volume of 23.7% and a time interval adjusted reduction of 44.0% (25.7%-62.2%), and an ADC drop of 180 × 10-6 mm2/s (14.2%). These data confirm that radiographic measurements are impacted by corticosteroids and provide benchmarks for the development of adjusted response criteria accounting for corticosteroid use.

Indexed as

Adrenal Cortex HormonesBrain NeoplasmsDiffusion Magnetic Resonance ImagingGlioblastomaAdultAgedContrast MediaFemaleFollow-Up StudiesHumansMaleMiddle AgedPrognosisRetrospective StudiesTumor BurdenAdrenal Cortex HormonesContrast Mediacorticosteroidsglioblastomaglucocorticoidsmagnetic resonance imagingpseudoresponse

Identifiers

PMID40443040
PMCPMC12908483

What OpenQuestion holds

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Registered trials

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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.