Evidence map›Paper›PMID 34940899›Full record

ArticleClinical neuroradiology2022

Differentiation of Cerebral Neoplasms with Vessel Size Imaging (VSI).

Asmaa Foda, Elias Kellner, Asanka Gunawardana, Xiang Gao, Martin Janz, Anna Kufner, Ahmed A Khalil, Rohat Geran, Ralf Mekle, Jochen B Fiebach and 1 more

Abstract read
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Article in Clinical neuroradiology, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing 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

4 citing papers in PubMed.

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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

11 authors.

Asmaa FodaInternational Graduate Program Medical Neurosciences, Charité - Universitätsmedizin Berlin, Hindenburgdamm 30, 12200, Berlin, Germany.ORCID http://orcid.org/0000-0003-1694-1983
Elias KellnerDepartment of Radiology, Medical Physics, University Medical Center Freiburg, Freiburg, Germany.
Asanka GunawardanaInstitute of Biometry and Clinical Epidemiology, Charité - Universitätsmedizin Berlin, Berlin, Germany.
Xiang GaoDepartment of Radiology, Medical Physics, University Medical Center Freiburg, Freiburg, Germany.
Martin JanzDepartment of Hematology, Oncology and Cancer Immunology, Charité - Universitätsmedizin Berlin, Berlin, Germany.
Anna KufnerCenter for Stroke Research Berlin, Charité - Universitätsmedizin Berlin, Berlin, Germany.
Ahmed A KhalilCenter for Stroke Research Berlin, Charité - Universitätsmedizin Berlin, Berlin, Germany.
Rohat GeranDepartment of Neurology with Experimental Neurology, Charité - Universitätsmedizin Berlin, Berlin, Germany.
Ralf MekleCenter for Stroke Research Berlin, Charité - Universitätsmedizin Berlin, Berlin, Germany.
Jochen B FiebachCenter for Stroke Research Berlin, Charité - Universitätsmedizin Berlin, Berlin, Germany.
Ivana GalinovicCenter for Stroke Research Berlin, Charité - Universitätsmedizin Berlin, Berlin, Germany.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

purposeCerebral neoplasms of various histological origins may show comparable appearances on conventional Magnetic Resonance Imaging (MRI). Vessel size imaging (VSI) is an MRI technique that enables noninvasive assessment of microvasculature by providing quantitative estimates of microvessel size and density. In this study, we evaluated the potential of VSI to differentiate between brain tumor types based on their microvascular morphology.

methodsUsing a clinical 3T MRI scanner, VSI was performed on 25 patients with cerebral neoplasms, 10 with glioblastoma multiforme (GBM), 8 with primary CNS lymphoma (PCNSL) and 7 with cerebral lung cancer metastasis (MLC). Following the postprocessing of VSI maps, mean vessel diameter (vessel size index, vsi) and microvessel density (Q) were compared across tumors, peritumoral areas, and healthy tissues.

resultsThe MLC tumors have larger and less dense microvasculature compared to PCNSLs in terms of vsi and Q (p = 0.0004 and p < 0.0001, respectively). GBM tumors have higher yet non-significantly different vsi values than PCNSLs (p = 0.065) and non-significant differences in Q. No statistically significant differences in vsi or Q were present between GBMs and MLCs. GBM tumor volume was positively correlated with vsi (r = 0.502, p = 0.0017) and negatively correlated with Q (r = -0.531, p = 0.0007).

conclusionConventional MRI parameters are helpful in differentiating between PCNSLs, GBMs, and MLCs. Additionally incorporating VSI parameters into the diagnostic protocol could help in further differentiating between PCNSLs and metastases and potentially between PCNSLs and GBMs. Future studies in larger patient cohorts are required to establish diagnostic cut-off values for VSI.

Indexed as

Brain NeoplasmsGlioblastomaSupratentorial NeoplasmsDiagnosis, DifferentialHumansMagnetic Resonance ImagingBrain imagingBrain tumorsDifferential diagnosisMagnetic resonance imagingMicrovasculature

Identifiers

PMID34940899
PMCPMC8894153

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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.