Evidence map›Paper›PMID 30054550›Full record

ArticleScientific reports2018

Evaluation and validation of HPV real-time PCR assay for the detection of HPV DNA in oral cytobrush and FFPE samples.

Alexandre Harlé, Julie Guillet, Jacques Thomas, Xavier Sastre-Garau, Marie Rouyer, Carole Ramacci, Pauline Gilson, Cindy Dubois, Gilles Dolivet, Agnès Leroux and 2 more

Abstract read
In one paragraph

Article in Scientific reports, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed, 1 pooled it
–field-weighted citation impact
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

9 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. Pooled it
  2. Article
  3. Article
  4. Article
  5. Article
  6. Article
  7. Article
  8. Article
  9. 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

12 authors.

Alexandre HarléUniversité de Lorraine, Nancy, France. a.harle@nancy.unicancer.fr.ORCID 0000-0001-9548-6522
Julie GuilletUniversité de Lorraine, Nancy, France.
Jacques ThomasService de Biopathologie, Institut de Cancérologie de Lorraine, Vandœuvre-les-Nancy, France.
Xavier Sastre-GarauService de Biopathologie, Institut de Cancérologie de Lorraine, Vandœuvre-les-Nancy, France.
Marie RouyerService de Biopathologie, Institut de Cancérologie de Lorraine, Vandœuvre-les-Nancy, France.
Carole RamacciService de Biopathologie, Institut de Cancérologie de Lorraine, Vandœuvre-les-Nancy, France.
Pauline GilsonUniversité de Lorraine, Nancy, France.
Cindy DuboisService de Biopathologie, Institut de Cancérologie de Lorraine, Vandœuvre-les-Nancy, France.
Gilles DolivetUniversité de Lorraine, Nancy, France.
Agnès LerouxService de Biopathologie, Institut de Cancérologie de Lorraine, Vandœuvre-les-Nancy, France.
Julia SalleronCellule data management et Biostatistique, Institut de Cancérologie de Lorraine, Vandœuvre-les-Nancy, France.
Jean-Louis MerlinUniversité de Lorraine, Nancy, France.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Specific HPV genotypes have been recognized as risk factors inducing head and neck cancers (HNC). The aim of this study was to validate a real-time PCR assay to detect accurately High Risk HPV DNA in Formalin Fixed Paraffin Embedded (FFPE) and oral cytobrush samples and compare the results with conventional PCR. Repeatability, reproducibility and limit of detection of Cobas assay were estimated for oral cytobrush and FFPE samples of patients with HNC. 53 samples of patients with a HNC were then used for assay comparison with conventional PCR. Finally, 26 samples of patients with anogenital neoplasia cancer were analyzed as control and assays comparison. Among the 53 samples of patients with HNC, 12 (26.7%) were HPV positive, 33 (73.3%) were HPV negative and 8 (15.1%) were non contributive with the Cobas assay. Among the 26 samples of patients with anogenital neoplasia, 15 (57.7%) were HPV positive and 11 were HPV negative (42.3%). One sample was found with an HPV 16 and HPV 18 co-infection. Only 3 samples were found with discrepant results. Cobas assay was found suitable for routine HPV detection with a very good repeatability and reproducibility for all HPV genotypes (CV < 0.6% and <0.4% respectively). Sensitivity and specificity for Cobas assay were 91.7% [61.5%;99.8%] and 96.9% [83.8%;99.9%] respectively. Ten nanograms of DNA were sufficient for the detection of HPV 16, HPV 18 and HPV in FFPE and oral cytobrush samples. Cobas assay was found comparable to conventional PCR and can detect accurately and rapidly HPV DNA in FFPE and oral cytobrush samples for the management of HNC and other types of HPV-associated neoplasia.

Indexed as

Real-Time Polymerase Chain ReactionAdultAgedAged, 80 and overDNA, ViralFemaleGenotypeHead and Neck NeoplasmsHuman papillomavirus 16Human papillomavirus 18HumansMaleMiddle AgedPapillomavirus InfectionsParaffin EmbeddingDNA, Viral

Identifiers

PMID30054550
PMCPMC6063863

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.