Evidence map›Paper›PMID 26581891›Full record

ArticleBMC cancer2015

The combination of four molecular markers improves thyroid cancer cytologic diagnosis and patient management.

Federica Panebianco, Chiara Mazzanti, Sara Tomei, Paolo Aretini, Sara Franceschi, Francesca Lessi, Giancarlo Di Coscio, Generoso Bevilacqua, Ivo Marchetti

Open access · goldAbstract read
In one paragraph

Article in BMC cancer, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 28 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
28citing papers in PubMed, 2 pooled it
6.0field-weighted citation impact, top 3% 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

28 citing papers in PubMed, 2 syntheses or guidelines pooled it, 52 citations in OpenAlex.

  1. Pooled it
  2. Pooled it
  3. Article
  4. Article
  5. Review
  6. Article
  7. Article
  8. Article
  9. Review
  10. Article
  11. Article
  12. Article
  13. Review
  14. Article
  15. Article
  16. Article
  17. Article
  18. Article
  19. Article
  20. 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 3 institutions in 2 countries.

Federica PanebiancoDivision of Surgical, Molecular, and Ultrastructural Pathology, University of Pisa and Pisa University Hospital, Via Roma 57, Pisa, 56100, Italy. panebiancof@upmc.edu.
Chiara MazzantiDivision of Surgical, Molecular, and Ultrastructural Pathology, University of Pisa and Pisa University Hospital, Via Roma 57, Pisa, 56100, Italy. c.mazzanti@fondazionepisascienza.org.
Sara TomeiSidra Medical and Research Center, Research Branch, Division of Translational Medicine, Al Corniche Street, PO 26999, Doha, Qatar. stomei@sidra.org.
Paolo AretiniPisa Science Foundation, Via Panfilo Castaldi 2, Pisa, 5612, Italy. p.aretini@fondazionepisascienza.org.
Sara FranceschiPisa Science Foundation, Via Panfilo Castaldi 2, Pisa, 5612, Italy. sara.franceschi@fondazionepisascienza.org.
Francesca LessiPisa Science Foundation, Via Panfilo Castaldi 2, Pisa, 5612, Italy. f.lessi@fondazionepisascienza.org.
Giancarlo Di CoscioSection of Cytopathology, University of Pisa and Pisa University Hospital, Via Roma 57, Pisa, 56100, Italy. g.dicoscio@ao-pisa.toscana.it.
Generoso BevilacquaDivision of Surgical, Molecular, and Ultrastructural Pathology, University of Pisa and Pisa University Hospital, Via Roma 57, Pisa, 56100, Italy. generoso.bevilacqua@med.unipi.it.
Ivo MarchettiDivision of Surgical, Molecular, and Ultrastructural Pathology, University of Pisa and Pisa University Hospital, Via Roma 57, Pisa, 56100, Italy. i.marchetti@ao-pisa.toscana.it.
University of Pisa · ITFondazione Pisa · ITSidra Medical and Research Center · QA

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundPapillary thyroid cancer is the most common endocrine malignancy. The most sensitive and specific diagnostic tool for thyroid nodule diagnosis is fine-needle aspiration (FNA) biopsy with cytological evaluation. Nevertheless, FNA biopsy is not always decisive leading to "indeterminate" or "suspicious" diagnoses in 10%-30% of cases. BRAF V600E detection is currently used as molecular test to improve the diagnosis of thyroid nodules, yet it lacks sensitivity. The aim of the present study was to identify novel molecular markers/computational models to improve the discrimination between benign and malignant thyroid lesions.

methodsWe collected 118 pre-operative thyroid FNA samples. All 118 FNA samples were characterized for the presence of the BRAF V600E mutation (exon15) by pyrosequencing and further assessed for mRNA expression of four genes (KIT, TC1, miR-222, miR-146b) by quantitative polymerase chain reaction. Computational models (Bayesian Neural Network Classifier, discriminant analysis) were built, and their ability to discriminate benign and malignant tumors were tested. Receiver operating characteristic (ROC) analysis was performed and principal component analysis was used for visualization purposes.

resultsIn total, 36/70 malignant samples carried the V600E mutation, while all 48 benign samples were wild type for BRAF exon15. The Bayesian neural network (BNN) and discriminant analysis, including the mRNA expression of the four genes (KIT, TC1, miR-222, miR-146b) showed a very strong predictive value (94.12% and 92.16%, respectively) in discriminating malignant from benign patients. The discriminant analysis showed a correct classification of 100% of the samples in the malignant group, and 95% by BNN. KIT and miR-146b showed the highest diagnostic accuracy of the ROC curve, with area under the curve values of 0.973 for KIT and 0.931 for miR-146b.

conclusionsThe four genes model proposed in this study proved to be highly discriminative of the malignant status compared with BRAF assessment alone. Its implementation in clinical practice can help in identifying malignant/benign nodules that would otherwise remain suspicious.

Indexed as

AgedBayes TheoremBiomarkers, TumorBiopsy, Fine-NeedleFemaleGene Expression ProfilingGenetic MarkersHumansMaleMicroRNAsMiddle AgedMutationNeoplasm ProteinsPrincipal Component AnalysisProto-Oncogene Proteins B-rafProto-Oncogene Proteins c-kitBiomarkers, TumorGenetic MarkersMicroRNAsMIR222, humanMIRN146 microRNA, humanNeoplasm ProteinsProto-Oncogene Proteins B-rafProto-Oncogene Proteins c-kitRNARNA, MitochondrialTCIM protein, human

Identifiers

PMID26581891
PMCPMC4652365
OpenAlexW2177709689

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.