Evidence map›Paper›PMID 35994156›Full record

ArticleJournal of neuro-oncology2022

The role of methylation profiling in histologically diagnosed neurocytoma: a case series.

Adam Z Kalawi, Denise M Malicki, Zied Abdullaev, Drew W Pratt, Martha Quezado, Kenneth Aldape, Jennifer D Elster, Megan R Paul, Paritosh C Khanna, Michael L Levy and 1 more

Open access · hybridAbstract read
In one paragraph

Article in Journal of neuro-oncology, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed, 1 pooled it
1.4field-weighted citation impact, top 18% of its field
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

10 citing papers in PubMed, 1 synthesis or guideline pooled it, 9 citations in OpenAlex.

  1. Pooled it
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  9. First-time identification of a KIF5B-NTRK2 fusion in extraventricular neurocytoma.Journal of neuropathology and experimental neurology · 2023
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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 at 4 institutions in 1 country.

Adam Z KalawiDivision of Child Neurology, Department of Neurosciences, University of California, San Diego, CA, USA. Azkalawi@health.ucsd.edu.
Denise M MalickiRady Children's Hospital, San Diego, CA, USA.
Zied AbdullaevLaboratory of Pathology, National Cancer Institute, Bethesda, MD, USA.
Drew W PrattDepartment of Pathology, University of Michigan, Ann Arbor, MI, USA.
Martha QuezadoLaboratory of Pathology, National Cancer Institute, Bethesda, MD, USA.
Kenneth AldapeLaboratory of Pathology, National Cancer Institute, Bethesda, MD, USA.
Jennifer D ElsterRady Children's Hospital, San Diego, CA, USA.
Megan R PaulRady Children's Hospital, San Diego, CA, USA.
Paritosh C KhannaRady Children's Hospital, San Diego, CA, USA.
Michael L LevyRady Children's Hospital, San Diego, CA, USA.
John R CrawfordDivision of Child Neurology, Department of Neurosciences, University of California, San Diego, CA, USA.
University of California, San Diego · USNational Cancer Institute · USRady Children's Hospital-San Diego · USUniversity of Michigan–Ann Arbor · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

purposeTo highlight the clinical, neuroradiographic, neuropathologic, and molecular features of histologically identified neurocytoma in a pediatric cohort and highlight the evolving use methylation profiling in providing diagnostic clarity in difficult to diagnosis pediatric brain tumors.

methodsFive consecutive children (ages 9-13, 2 girls 3 boys) were histologically diagnosed with neurocytoma at Rady Children's Hospital San Diego from 2012 to 2018. Clinical and molecular features were analyzed with regards to treatment course and outcome.

resultsPresenting symptoms included seizures (n = 2), syncope (n = 1), headache (n = 2), visual disturbances (n = 2) and emesis (n = 2). Tumor location included intraventricular (n = 2), intraventricular with parenchymal spread (n = 1), and extraventricular (n = 2). Magnetic resonance imaging demonstrated reduced diffusivity (2/5), signal abnormality on susceptibility-weighted sequences (3/5), and varying degrees of contrast enhancement (4/5). All patients underwent surgical resection alone. Recurrence occurred in four children that were treated with surgery (4/4), adjuvant radiation (2/4), and chemoradiation (1/4). Neuropathologic features included positivity for GFAP (4/5), synaptophysin (4/5), NSE (2/2), NeuN (4/4), and variable Ki-67 (< 1% to 15%). Next generation sequencing (3/5) and microarray (3/5) collectively were abnormal in four of five tumors. Methylation profiling was successfully performed on four of five samples which led to modification of diagnosis in two patients and the others were either unclassifiable or confirmatory with the histologic diagnosis. Mean time to follow up was 77 months (range 44-112 months). Mean progression free survival and overall survival were 24 months (range 6 to 52 months) and 100% respectively.

conclusionNeurocytomas are a rare clinical entity that warrants further investigation into molecular and pathologic prognosticating features. Methylation profiling may aid in differentiation of neurocytoma from other difficult to diagnose tumors who share similar histologic features.

Indexed as

Brain NeoplasmsNeurocytomaChildFemaleHumansKi-67 AntigenMagnetic Resonance ImagingMaleMethylationSynaptophysinKi-67 AntigenSynaptophysinAtypical neurocytomaMethylationNeurocytomaPediatric brain tumorPediatric neurocytoma

Identifiers

PMID35994156
PMCPMC9477906
OpenAlexW4292583653

What OpenQuestion holds

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LicenceCC BY
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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.