Evidence map›Paper›PMID 35805032›Full record

ArticleCancers2022

Evaluation Criteria for Chromosome Instability Detection by FISH to Predict Malignant Progression in Premalignant Glottic Laryngeal Lesions.

Verona E Bergshoeff, Maschenka C A Balkenhol, Annick Haesevoets, Andrea Ruland, Michelene N Chenault, Rik C Nelissen, Carine J Peutz, Ruud Clarijs, Jeroen A W M Van der Laak, Robert P Takes and 5 more

Open access · goldAbstract read
In one paragraph

Article in Cancers, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
0.2field-weighted citation impact, top 51% 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

1 citing paper in PubMed, 1 citations in OpenAlex.

  1. 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

15 authors at 5 institutions in 2 countries.

Verona E BergshoeffDepartment of Otorhinolaryngology, Head and Neck Surgery, GROW-School for Oncology & Developmental Biology, Maastricht University Medical Center, 6229 HX Maastricht, The Netherlands.
Maschenka C A BalkenholDepartment of Otorhinolaryngology, Head and Neck Surgery, GROW-School for Oncology & Developmental Biology, Maastricht University Medical Center, 6229 HX Maastricht, The Netherlands.ORCID 0000-0001-9457-618X
Annick HaesevoetsDepartment of Pathology, GROW-School for Oncology & Developmental Biology, Maastricht University Medical Center, 6229 HX Maastricht, The Netherlands.
Andrea RulandDepartment of Pathology, GROW-School for Oncology & Developmental Biology, Maastricht University Medical Center, 6229 HX Maastricht, The Netherlands.
Michelene N ChenaultDepartment of Otorhinolaryngology, Head and Neck Surgery, GROW-School for Oncology & Developmental Biology, Maastricht University Medical Center, 6229 HX Maastricht, The Netherlands.
Rik C NelissenDepartment of Otorhinolaryngology, Head and Neck Surgery, GROW-School for Oncology & Developmental Biology, Maastricht University Medical Center, 6229 HX Maastricht, The Netherlands.
Carine J PeutzDepartment of Pathology, GROW-School for Oncology & Developmental Biology, Maastricht University Medical Center, 6229 HX Maastricht, The Netherlands.
Ruud ClarijsDepartment of Pathology, Zuyderland Medical Center, 6419 PC Heerlen, The Netherlands.
Jeroen A W M Van der LaakDepartment of Pathology, Radboud University Medical Center, 6225 GA Nijmegen, The Netherlands.
Robert P TakesDepartment of Otorhinolaryngology and Head and Neck Surgery, Radboud University Medical Center, 6225 GA Nijmegen, The Netherlands.
Michiel W Van den BrekelDepartment of Head and Neck Oncology and Surgery, The Netherlands Cancer Institute, 1066 CX Amsterdam, The Netherlands.ORCID 0000-0002-6338-6743
Marie-Louise F Van VelthuysenDepartment of Pathology, Erasmus University Medical Center, 3015 GD Rotterdam, The Netherlands.ORCID 0000-0003-0435-9494
Frans C S RamaekersDepartment of Molecular Cell Biology, GROW-School for Oncology & Developmental Biology, Maastricht University Medical Center, 6229 HX Maastricht, The Netherlands.
Bernd KremerDepartment of Otorhinolaryngology, Head and Neck Surgery, GROW-School for Oncology & Developmental Biology, Maastricht University Medical Center, 6229 HX Maastricht, The Netherlands.
Ernst-Jan M SpeelDepartment of Pathology, GROW-School for Oncology & Developmental Biology, Maastricht University Medical Center, 6229 HX Maastricht, The Netherlands.ORCID 0000-0002-3016-2989
Maastricht University · NLRadboud University Nijmegen · NLErasmus MC · NLThe Netherlands Cancer Institute · NLZuyderland Medisch Centrum · NL

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: The definition of objective, clinically applicable evaluation criteria for FISH 1c/7c in laryngeal precursor lesions for the detection of chromosome instability (CI). Copy Number Variations (CNV) for chromosomes 1 and 7 reflect the general ploidy status of premalignant head and neck lesions and can therefore be used as a marker for CI. Methods: We performed dual-target FISH for chromosomes 1 and 7 centromeres on 4 µm formalin-fixed, paraffin-embedded tissue sections of 87 laryngeal premalignancies to detect CNVs. Thirty-five normal head and neck squamous cell samples were used as a control. First, the chromosome 7:1 ratio (CR) was evaluated per lesion. The normal range of CRs (≥0.84 ≤ 1.16) was based on the mean CR +/− 3 x SD found in the normal population. Second, the percentage of aberrant nuclei, harboring > 2 chromosomes of chromosome 1 and/or 7 (PAN), was established (cut-off value for abnormal PAN ≥ 10%). Results: PAN showed a stronger correlation with malignant progression than CR (resp. OR 5.6, p = 0.001 and OR 3.8, p = 0.009). PAN combined with histopathology resulted in a prognostic model with an area under the ROC curve (AUC) of 0.75 (s.e. 0.061, sensitivity 71%, specificity 70%). Conclusions: evaluation criteria for FISH 1c/7c based on PAN ≥ 10% provide the best prognostic information on the risk of malignant progression of premalignant laryngeal lesions as compared with criteria based on the CR. FISH 1c/7c detection can be applied in combination with histopathological assessment.

Indexed as

chromosome instabilitydysplasiaFISHhead and neck cancerlarynxpremalignant

Identifiers

PMID35805032
PMCPMC9265082
OpenAlexW4283793554

What OpenQuestion holds

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LicenceCC BY
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Registered trials

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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.