Evidence map›Paper›PMID 35318454›Full record

ArticleLaboratory investigation; a journal of technical methods and pathology2022

The diagnostic utility of DNA copy number analysis of core needle biopsies from soft tissue and bone tumors.

Jan Köster, Paul Piccinelli, Linda Arvidsson, Fredrik Vult von Steyern, Camila Bedeschi Rego De Mattos, Martin Almquist, Jenny Nilsson, Linda Magnusson, Fredrik Mertens

Open access · hybridAbstract read
In one paragraph

Article in Laboratory investigation; a journal of technical methods and pathology, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
0.5field-weighted citation impact, top 38% 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

3 citing papers in PubMed, 3 citations in OpenAlex.

  1. Transcriptomic Subgroups in Soft Tissue Tumors Correlate with Morphologic Subtype, Genomic Features, and Outcome.Clinical cancer research : an official journal of the American Association for Cancer Research · 2026
    Article
  2. Reporting Bone Cytopathology-A Proposal Based on a Single Tertiary Centre Experience.Cytopathology : official journal of the British Society for Clinical Cytology · 2025
    Article
  3. 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

9 authors at 2 institutions in 1 country.

Jan KösterDivision of Clinical Genetics, Department of Laboratory Medicine, Lund University, Lund, Sweden. jan.koster@med.lu.se.ORCID 0000-0002-0886-2794
Paul PiccinelliDivision of Clinical Genetics, Department of Laboratory Medicine, Lund University, Lund, Sweden.
Linda ArvidssonDepartment of Clinical Genetics and Pathology, Division of Laboratory Medicine, Lund, Sweden.
Fredrik Vult von SteyernDepartment of Orthopedics, Department of Clinical Sciences Lund, Skåne University Hospital, Lund, Sweden.
Camila Bedeschi Rego De MattosDepartment of Orthopedics, Department of Clinical Sciences Lund, Skåne University Hospital, Lund, Sweden.
Martin AlmquistDepartment of Surgery, Skåne University Hospital, Lund, Sweden.
Jenny NilssonDivision of Clinical Genetics, Department of Laboratory Medicine, Lund University, Lund, Sweden.
Linda MagnussonDivision of Clinical Genetics, Department of Laboratory Medicine, Lund University, Lund, Sweden.
Fredrik MertensDivision of Clinical Genetics, Department of Laboratory Medicine, Lund University, Lund, Sweden.ORCID 0000-0002-6278-5232
Lund University · SESkåne University Hospital · SE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Morphologic and immunohistochemical analysis of preoperative core needle biopsies (CNB) is important in the management of patients with soft tissue and bone tumors (STBTs). Most SBTB subtypes have more or less extensive DNA copy number aberrations (CNA), potentially providing useful diagnostic information. To evaluate the technical feasibility of single nucleotide polymorphism (SNP) array analysis and the diagnostic usefulness of the copy number profiles, we studied CNBs from 171 patients with suspected STBTs. SNP array analysis could be performed on 168 (98%) of the samples. The CNA profile was compatible with the CNB diagnosis in 87% of the cases. Discrepant cases were dominated by false-negative results due to nonrepresentative material or contamination with normal cells. 70 genomic profiles were indicative of specific histopathologic tumor entities and in agreement with the corresponding CNB diagnoses in 83%. In 96 of the cases with aberrant CNA profiles, the SNP profiles were of sufficient quality for segmentation, allowing clustering analysis on the basis of the Jaccard similarity index. The analysis of these segment files showed three major CNA clusters, based on the complexity levels and the predominance of gains versus losses. For 43 of these CNB samples, we had SNP array data also from their corresponding surgical samples. In 33 of these pairs, the two corresponding samples clustered next to each other, with Jaccard scores ranging from 0.61 to 0.99 (median 0.96). Also, for those tumor pairs that did not cluster together, the Jaccard scores were relatively high (median 0.9). 10 cases showed discrepant results, mainly due to varying degrees of normal cell contamination or technical issues. Thus, the copy number profile seen in a CNB is typically highly representative of the major cell population in the tumor.

Indexed as

Bone NeoplasmsSoft Tissue NeoplasmsBiopsy, Large-Core NeedleDNA Copy Number VariationsHumansRetrospective Studies

Identifiers

PMID35318454
PMCPMC9309094
OpenAlexW4221013520

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.