Evidence map›Paper›PMID 37287574›Full record

ArticleNeuro-oncology advances2023

Spinal meningiomas.

Christoph Hohenberger, Peter Hau, Karl-Michael Schebesch, Oliver Kölbl, Markus J Riemenschneider, Fabian Pohl, Martin Proeschold, Nils Ole Schmidt

Open access · goldAbstract read
In one paragraph

Article in Neuro-oncology advances, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed
2.4field-weighted citation impact, top 11% 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, 11 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Article
  6. Lumbar angiomatous meningioma: how to manage this rare entity? A case report.International journal of surgery case reports · 2025
    Article
  7. Review
  8. Article
  9. Clear cell meningiomas-case presentation, review of radiographic identifiers, and treatment approaches.Child's nervous system : ChNS : official journal of the International Society for Pediatric Neurosurgery · 2024
    Review
  10. 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

8 authors at 1 institution in 1 country.

Christoph HohenbergerDepartment of Neurosurgery, University Medical Center Regensburg, Regensburg, Germany.
Peter HauBrain Tumor Center, University Medical Center Regensburg, Regensburg, Germany.ORCID https://orcid.org/0000-0003-3894-5053
Karl-Michael SchebeschDepartment of Neurosurgery, University Medical Center Regensburg, Regensburg, Germany.
Oliver KölblDepartment of Radiotherapy, University Medical Center Regensburg, Regensburg, Germany.
Markus J RiemenschneiderDepartment of Neuropathology, University Medical Center Regensburg, Regensburg, Germany.
Fabian PohlDepartment of Radiotherapy, University Medical Center Regensburg, Regensburg, Germany.
Martin ProescholdDepartment of Neurosurgery, University Medical Center Regensburg, Regensburg, Germany.
Nils Ole SchmidtDepartment of Neurosurgery, University Medical Center Regensburg, Regensburg, Germany.
University Hospital Regensburg · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Spinal meningiomas (SM) are lesions with a mostly favorable oncological and surgical prognosis and a low incidence of tumor recurrence. SM account for approximately 1.2-12.7% of all meningiomas and 25% of all spinal cord tumors. Typically, SM are located in the intradural extramedullary space. SM grow slowly and spread laterally into the subarachnoid space, stretching and sometimes incorporating the surrounding arachnoid but rarely the pia. Standard treatment is surgery with the primary aims of achieving complete tumor resection as well as improving and recovering neurologic function. Radiotherapy may be considered in case of tumor recurrence, for challenging surgical cases, and for patients with higher-grade lesions (World Health Organization grade 2 or 3); however, radiotherapy is mostly used as an adjuvant therapy for SM. New molecular and genetic profiling increases the understanding of SM and may uncover additional treatment options.

Indexed as

molecular and genetic targetsrecurrence ratesurgical therapy

Identifiers

PMID37287574
PMCPMC10243846
OpenAlexW4379769018

What OpenQuestion holds

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LicenceCC BY-NC
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.