Evidence map›Paper›PMID 30152874›Full record

ArticleHistopathology2019

Does CSF1 overexpression or rearrangement influence biological behaviour in tenosynovial giant cell tumours of the knee?

Monique J L Mastboom, Daisy M Hoek, Judith V M G Bovée, Michiel A J van de Sande, Károly Szuhai

Open access · bronzeAbstract read
In one paragraph

Article in Histopathology, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 25 papers.

0numbers the graph read from it
0cells of the map it votes in
25citing papers in PubMed
3.4field-weighted citation impact, top 8% 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

25 citing papers in PubMed, 41 citations in OpenAlex.

  1. Trial
  2. Review
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  4. TGCT of the shoulder - a case series and literature review.Archives of orthopaedic and trauma surgery · 2026
    Review
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  7. Observational
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  10. Observational
  11. Article
  12. Article
  13. Observational
  14. Article
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  16. Role of colony-stimulating factor 1 in the neoplastic process of tenosynovial giant cell tumor.Tumour biology : the journal of the International Society for Oncodevelopmental Biology and Medicine · 2022
    Article
  17. Article
  18. Article
  19. PDGFB RNA in situ hybridization for the diagnosis of dermatofibrosarcoma protuberans.Modern pathology : an official journal of the United States and Canadian Academy of Pathology, Inc · 2021
    Article
  20. Observational
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

5 authors at 1 institution in 1 country.

Monique J L MastboomDepartment of Orthopaedic Surgery, Leiden University Medical Center, Leiden, the Netherlands.ORCID http://orcid.org/0000-0002-8980-3955
Daisy M HoekDepartment of Cell and Chemical biology, Leiden University Medical Center, Leiden, the Netherlands.
Judith V M G BovéeDepartment of Pathology, Leiden University Medical Center, Leiden, the Netherlands.
Michiel A J van de SandeDepartment of Orthopaedic Surgery, Leiden University Medical Center, Leiden, the Netherlands.
Károly SzuhaiDepartment of Cell and Chemical biology, Leiden University Medical Center, Leiden, the Netherlands.ORCID http://orcid.org/0000-0002-1228-4245
Leiden University Medical Center · NL

Funding

Daiichi SankyoLeiden University Medical Center (LUMC)
6 · The paper itself

Abstract

aimsLocalised- and diffuse-type tenosynovial giant cell tumours (TGCT) are regarded as different clinical and radiological TGCT types. However, genetically and histopathologically they seem indistinguishable. We aimed to correlate CSF1 expression and CSF1 rearrangement with the biological behaviour of different TGCT-types with clinical outcome (recurrence). METHODS AND

resultsAlong a continuum of extremes, therapy-naive knee TGCT patients with >3-year follow-up, mean age 43 (range = 6-71) years and 56% females were selected. Nine localised (two recurrences), 16 diffuse-type (nine recurrences) and four synovitis as control were included. Rearrangement of the CSF1 locus was evaluated with split-apart fluorescence in-situ hybridisation (FISH) probes. Regions were selected to score after identifying CSF1-expressing regions, using mRNA ISH with the help of digital correlative microscopy. CSF1 rearrangement was considered positive in samples containing >2 split signals/100 nuclei. Irrespective of TGCT-subtype, all cases showed CSF1 expression and in 76% CSF1 rearrangement was detected. Quantification of CSF1-expressing cells was not informative, due to the extensive intratumour heterogeneity. Of the four synovitis cases, two also showed CSF1 expression without CSF1 rearrangement. No correlation between CSF1 expression or rearrangement with clinical subtype and local recurrence was detected. Both localised and diffuse TGCT cases showed a scattered distribution in the tissue of CSF1-expressing cells.

conclusionIn diagnosing TGCT, CSF1 mRNA-ISH, in combination with CSF1 split-apart FISH using digital correlative microscopy, is an auxiliary diagnostic tool to identify rarely occurring neoplastic cells. This combined approach allowed us to detect CSF1 rearrangement in 76% of the TGCT cases. Neither CSF1 expression nor presence of CSF1 rearrangement could be associated with the difference in biological behaviour of TGCT.

Indexed as

AdolescentAdultAgedChildFemaleGene RearrangementGiant Cell Tumor of Tendon SheathHumansKneeMacrophage Colony-Stimulating FactorMaleMiddle AgedSoft Tissue NeoplasmsSynovial MembraneYoung AdultCSF1 protein, humanMacrophage Colony-Stimulating Factorcolony stimulating factor 1FISHgiant cell tumour of tendon sheathmRNA ISHpigmented villonodularrare diseasessynovitistenosynovial giant cell tumour

Identifiers

PMID30152874
PMCPMC7379608
OpenAlexW2889391793

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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.